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### Running command:
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###   /Library/Frameworks/R.framework/Resources/bin/R CMD check --install=check:MungeSumstats.install-out.txt --library=/Library/Frameworks/R.framework/Resources/library --no-vignettes --timings MungeSumstats_1.4.5.tar.gz
###
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* using log directory ‘/Users/biocbuild/bbs-3.15-bioc/meat/MungeSumstats.Rcheck’
* using R version 4.2.1 (2022-06-23)
* using platform: x86_64-apple-darwin17.0 (64-bit)
* using session charset: UTF-8
* using option ‘--no-vignettes’
* checking for file ‘MungeSumstats/DESCRIPTION’ ... OK
* checking extension type ... Package
* this is package ‘MungeSumstats’ version ‘1.4.5’
* package encoding: UTF-8
* checking package namespace information ... OK
* checking package dependencies ... OK
* checking if this is a source package ... OK
* checking if there is a namespace ... OK
* checking for hidden files and directories ... OK
* checking for portable file names ... OK
* checking for sufficient/correct file permissions ... OK
* checking whether package ‘MungeSumstats’ can be installed ... OK
* checking installed package size ... OK
* checking package directory ... OK
* checking ‘build’ directory ... OK
* checking DESCRIPTION meta-information ... OK
* checking top-level files ... OK
* checking for left-over files ... OK
* checking index information ... OK
* checking package subdirectories ... OK
* checking R files for non-ASCII characters ... OK
* checking R files for syntax errors ... OK
* checking whether the package can be loaded ... OK
* checking whether the package can be loaded with stated dependencies ... OK
* checking whether the package can be unloaded cleanly ... OK
* checking whether the namespace can be loaded with stated dependencies ... OK
* checking whether the namespace can be unloaded cleanly ... OK
* checking dependencies in R code ... OK
* checking S3 generic/method consistency ... OK
* checking replacement functions ... OK
* checking foreign function calls ... OK
* checking R code for possible problems ... OK
* checking Rd files ... OK
* checking Rd metadata ... OK
* checking Rd cross-references ... OK
* checking for missing documentation entries ... OK
* checking for code/documentation mismatches ... OK
* checking Rd \usage sections ... OK
* checking Rd contents ... OK
* checking for unstated dependencies in examples ... OK
* checking contents of ‘data’ directory ... OK
* checking data for non-ASCII characters ... OK
* checking data for ASCII and uncompressed saves ... OK
* checking R/sysdata.rda ... OK
* checking files in ‘vignettes’ ... OK
* checking examples ... OK
Examples with CPU (user + system) or elapsed time > 5s
                     user system elapsed
get_genome_builds 101.407  6.355 108.171
format_sumstats    61.253  3.850  65.252
read_vcf            7.355  0.135  18.032
* checking for unstated dependencies in ‘tests’ ... OK
* checking tests ...
  Running ‘testthat.R’
 OK
* checking for unstated dependencies in vignettes ... OK
* checking package vignettes in ‘inst/doc’ ... OK
* checking running R code from vignettes ... SKIPPED
* checking re-building of vignette outputs ... SKIPPED
* checking PDF version of manual ... OK
* DONE

Status: OK

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### Running command:
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###   /Library/Frameworks/R.framework/Resources/bin/R CMD INSTALL MungeSumstats
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* installing to library ‘/Library/Frameworks/R.framework/Versions/4.2/Resources/library’
* installing *source* package ‘MungeSumstats’ ...
** using staged installation
** R
** data
** inst
** byte-compile and prepare package for lazy loading
** help
*** installing help indices
** building package indices
** installing vignettes
** testing if installed package can be loaded from temporary location
** testing if installed package can be loaded from final location
** testing if installed package keeps a record of temporary installation path
* DONE (MungeSumstats)

R version 4.2.1 (2022-06-23) -- "Funny-Looking Kid"
Copyright (C) 2022 The R Foundation for Statistical Computing
Platform: x86_64-apple-darwin17.0 (64-bit)

R is free software and comes with ABSOLUTELY NO WARRANTY.
You are welcome to redistribute it under certain conditions.
Type 'license()' or 'licence()' for distribution details.

R is a collaborative project with many contributors.
Type 'contributors()' for more information and
'citation()' on how to cite R or R packages in publications.

Type 'demo()' for some demos, 'help()' for on-line help, or
'help.start()' for an HTML browser interface to help.
Type 'q()' to quit R.

> library(testthat)
> library(MungeSumstats)
> 
> test_check("MungeSumstats")
Collecting metadata from Open GWAS.
Filtering metadata by substring criteria.
Found 3 GWAS datasets matching search criteria across:
   - 3 trait(s)
   - 1 population(s)
   - 2 category(ies)
   - 2 subcategory(ies)
   - 2 publication(s)
   - 2 consortia(ium)
   - 1 genome build(s)
Collecting metadata from Open GWAS.
Filtering metadata by substring criteria.
Filtering metadata by sample/case/control/SNP size criteria.
Excluding sample/case/control size with NAs.
Found 3 GWAS datasets matching search criteria across:
   - 3 trait(s)
   - 1 population(s)
   - 2 category(ies)
   - 2 subcategory(ies)
   - 2 publication(s)
   - 2 consortia(ium)
   - 1 genome build(s)
Collecting metadata from Open GWAS.
Filtering metadata by substring criteria.
Found 45 GWAS datasets matching search criteria across:
   - 42 trait(s)
   - 3 population(s)
   - 2 category(ies)
   - 2 subcategory(ies)
   - 7 publication(s)
   - 5 consortia(ium)
   - 1 genome build(s)
Downloading VCF ==> /tmp/RtmpXFes5o/ieu-a-298.vcf.gz
Downloading with download.file.
trying URL 'https://gwas.mrcieu.ac.uk/files/ieu-a-298/ieu-a-298.vcf.gz'
Content type 'application/gzip' length 234480 bytes (228 KB)
==================================================
downloaded 228 KB

Downloading VCF index ==> https://gwas.mrcieu.ac.uk/files/ieu-a-298/ieu-a-298.vcf.gz.tbi
Downloading with download.file.
trying URL 'https://gwas.mrcieu.ac.uk/files/ieu-a-298/ieu-a-298.vcf.gz.tbi'
Content type 'application/gzip' length 37803 bytes (36 KB)
==================================================
downloaded 36 KB

Processing 1 datasets from Open GWAS.

========== Processing dataset : a-fake-id ==========

Downloading VCF ==> /tmp/RtmpXFes5o/a-fake-id.vcf.gz
Downloading with download.file.
trying URL 'https://gwas.mrcieu.ac.uk/files/a-fake-id/a-fake-id.vcf.gz'
Processing 1 datasets from Open GWAS.

========== Processing dataset : ieu-a-298 ==========

Using previously downloaded VCF.
Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/ieu-a-298/ieu-a-298.tsv.gz
File already tabix-indexed.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.4 secs
5 empty column(s) detected.
1 sample detected: ieu-a-298
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 3.6 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 1.1 secs
Dropping 1 duplicate columns.
Checking for empty columns.
Removing 1 empty columns.
Unlisting 4 columns.
Renaming ID as SNP.
VCF file has -log10 P-values, these will be  converted to unadjusted p-values in the 'P' column.
No INFO (SI) column detected.
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	chr	BP	end	REF	ALT	FILTER	ES	SE	LP	SS	P	
Summary statistics report:
   - 10,684 rows
   - 10,684 unique variants
   - 553 genome-wide significant variants (P<5e-8)
   - 22 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Ensuring that the N column is all integers.
The sumstats N column is not all integers, this could effect downstream analysis. These will be converted to integers.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
N already exists within sumstats_dt.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/ieu-a-298/ieu-a-298.tsv.gz
Summary statistics report:
   - 10,684 rows (100% of original 10,684 rows)
   - 10,684 unique variants
   - 553 genome-wide significant variants (P<5e-8)
   - 22 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR      BP A1 A2     END FILTER   BETA     SE      LP     N
1: rs76805690   1 2256288  C  A 2256288   PASS 0.0389 0.0175 1.58536 74046
2: rs75379543   1 2261983  C  A 2261983   PASS 0.0427 0.0167 1.96738 74046
3: rs75273719   1 2263666  G  A 2263666   PASS 0.0502 0.0171 2.47353 74046
4:   rs903904   1 2263888  C  T 2263888   PASS 0.0413 0.0169 1.82769 74046
             P
1: 0.025980051
2: 0.010780031
3: 0.003361012
4: 0.014869967
Returning path to saved data.

ieu-a-298 : Done in 0.09 minutes.

Done with all processing in 0.09 minutes.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77847bf3399a.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778465449e46
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A0	A1	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77847bf3399a.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784469d93db.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778465449e46
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784469d93db.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77844102ce76.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778441d1fc2c
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A2	A1	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for correct direction of A1 (reference) and A2 (alternative allele).
Loading reference genome data.
There are 47 SNPs where A1 doesn't match the reference genome.
These will be flipped with their effect columns.
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Warning: When method is an integer, must be >0.
67 SNPs (72%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77844102ce76.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  G  A 0.63060 -0.017 0.003 2.359e-10
3: rs34305371   1 72733610  G  A 0.91231 -0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784591aeac.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778441d1fc2c
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Ensuring all SNPs are on the reference genome.
Loading reference genome data.
Checking for correct direction of A1 (reference) and A2 (alternative allele).
There are 46 SNPs where A1 doesn't match the reference genome.
These will be flipped with their effect columns.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Warning: When method is an integer, must be >0.
67 SNPs (72%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784591aeac.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  G  A 0.63060 -0.017 0.003 2.359e-10
3: rs34305371   1 72733610  G  A 0.91231 -0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778438409be6.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77847b01e099
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Loading reference genome data.
1 SNPs are non-biallelic. These will be removed.
Writing in tabular format ==>  /tmp/RtmpXFes5o/snp_bi_allelic.tsv.gz
Warning: When method is an integer, must be >0.
46 SNPs (50%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778438409be6.tsv.gz
Summary statistics report:
   - 92 rows (98.9% of original 93 rows)
   - 92 unique variants
   - 69 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784736ddb37.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77847b01e099
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Loading reference genome data.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784736ddb37.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77843f2096ab.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778452f0ccf7
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Ensuring parameters comply with LDSC format.
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
1 SNP IDs are not correctly formatted. These will be corrected from the reference genome.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Ensuring all SNPs are on the reference genome.
Loading reference genome data.
Checking for correct direction of A1 (reference) and A2 (alternative allele).
There are 46 SNPs where A1 doesn't match the reference genome.
These will be flipped with their effect columns.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Computing Z-score from P using formula: `sign(BETA)*sqrt(stats::qchisq(P,1,lower=FALSE)`
Assigning N=1001 for all SNPs.
67 SNPs (72%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77843f2096ab.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P IMPUTATION_SNP
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08             NA
2: rs11210860   1 43982527  G  A 0.63060 -0.017 0.003 2.359e-10             NA
3: rs34305371   1 72733610  G  A 0.91231 -0.035 0.005 3.762e-14             NA
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08             NA
   flipped         Z IMPUTATION_z_score    N
1:      NA  5.630777               TRUE 1001
2:    TRUE -6.335939               TRUE 1001
3:    TRUE -7.568968               TRUE 1001
4:      NA -5.630488               TRUE 1001
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77842b735b20.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77844d613f10
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	N_CON	N_CAS	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Ensuring all SNPs are on the reference genome.
Loading reference genome data.
Checking for correct direction of A1 (reference) and A2 (alternative allele).
There are 46 SNPs where A1 doesn't match the reference genome.
These will be flipped with their effect columns.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Computing effective sample size using the LDSC method:
 Neff = (N_CAS+N_CON) * (N_CAS/(N_CAS+N_CON)) / mean((N_CAS/(N_CAS+N_CON))[(N_CAS+N_CON)==max(N_CAS+N_CON)]))
Computing sample size using the sum method:
 N = N_CAS + N_CON
Computing effective sample size using the GIANT method:
 Neff = 2 / (1/N_CAS + 1/N_CON)
Computing effective sample size using the METAL method:
 Neff = 4 / (1/N_CAS + 1/N_CON)
67 SNPs (72%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77842b735b20.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P N_CON N_CAS
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08   100   120
2: rs11210860   1 43982527  G  A 0.63060 -0.017 0.003 2.359e-10   100   120
3: rs34305371   1 72733610  G  A 0.91231 -0.035 0.005 3.762e-14   100   120
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08   100   120
   Neff_ldsc   N Neff_giant Neff_metal
1:       220 220        109        218
2:       220 220        109        218
3:       220 220        109        218
4:       220 220        109        218
Returning path to saved data.
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.4 secs
6 empty column(s) detected.
1 sample detected: EBI-a-GCST005647
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 2.6 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.3 secs
Dropping 2 duplicate columns.
Checking for empty columns.
Unlisting 4 columns.
Renaming ID as SNP.
VCF file has -log10 P-values, these will be  converted to unadjusted p-values in the 'P' column.
No INFO (SI) column detected.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784bc7cabf.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77842f8bee44
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	chr	BP	end	REF	ALT	FILTER	AF	ES	LP	SE	P	N	
Summary statistics report:
   - 101 rows
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
N already exists within sumstats_dt.
2 SNPs (2%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784bc7cabf.tsv.gz
Summary statistics report:
   - 101 rows (100% of original 101 rows)
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
           SNP CHR    BP A1 A2   END FILTER    FRQ    BETA       LP     SE
1:  rs58108140   1 10583  G  A 10583   PASS 0.1589  0.0312 0.369267 0.0393
2:    rs806731   1 30923  G  T 30923   PASS 0.7843 -0.0114 0.126854 0.0353
3: rs116400033   1 51479  T  A 51479   PASS 0.1829  0.0711 1.262410 0.0370
4: rs146477069   1 54421  A  G 54421   PASS 0.0352 -0.0240 0.112102 0.0830
            P      N
1: 0.42730011 293723
2: 0.74669974 293723
3: 0.05464998 293723
4: 0.77249913 293723
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77843351e39c.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77842f8bee44
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	chr	BP	end	REF	ALT	FILTER	AF	ES	LP	P	N	
Summary statistics report:
   - 101 rows
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
The sumstats SE column is not present...Deriving SE from Beta and P
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
N already exists within sumstats_dt.
2 SNPs (2%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77843351e39c.tsv.gz
Summary statistics report:
   - 101 rows (100% of original 101 rows)
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
           SNP CHR    BP A1 A2   END FILTER    FRQ    BETA       LP          P
1:  rs58108140   1 10583  G  A 10583   PASS 0.1589  0.0312 0.369267 0.42730011
2:    rs806731   1 30923  G  T 30923   PASS 0.7843 -0.0114 0.126854 0.74669974
3: rs116400033   1 51479  T  A 51479   PASS 0.1829  0.0711 1.262410 0.05464998
4: rs146477069   1 54421  A  G 54421   PASS 0.0352 -0.0240 0.112102 0.77249913
        N         SE IMPUTATION_SE
1: 293723 0.03930361          TRUE
2: 293723 0.03529477          TRUE
3: 293723 0.03699948          TRUE
4: 293723 0.08301411          TRUE
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778455cea4c3.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77842f8bee44
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	CHR	BP	A1	A2	FRQ	Z	SE	P	N	
Summary statistics report:
   - 25 rows
   - 25 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
The sumstats BETA column is not present...Deriving BETA from Z and SE
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
N already exists within sumstats_dt.
13 SNPs (52%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778455cea4c3.tsv.gz
Summary statistics report:
   - 25 rows (100% of original 25 rows)
   - 25 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
           SNP CHR     BP A1 A2       FRQ      Z          SE      P      N
1:  rs12184267   1 715265  C  T 0.9591931 -0.916 0.007518884 0.3598 225955
2:  rs12184277   1 715367  A  G 0.9589313 -0.656 0.007491601 0.5116 226215
3:  rs12184279   1 717485  C  A 0.9594241 -1.050 0.007534860 0.2938 226224
4: rs116801199   1 720381  G  T 0.9578380 -0.300 0.007391344 0.7644 226626
           BETA IMPUTATION_BETA
1: -0.006887298            TRUE
2: -0.004914490            TRUE
3: -0.007911603            TRUE
4: -0.002217403            TRUE
Returning path to saved data.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Sorting coordinates.
Filtering SNPs based on INFO score.
46 SNPs are below the INFO threshold of 0.9 and will be removed.
Writing in tabular format ==>  /tmp/RtmpXFes5o/info_filter.tsv.gz
INFO_filter==0. Skipping INFO score filtering step.
Filtering SNPs based on INFO score.
All rows have INFO>=0.9
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Sorting coordinates.
3 p-values are >1 which LDSC/MAGMA may not be able to handle. These will be converted to 1.
5 p-values are <0 which LDSC/MAGMA may not be able to handle. These will be converted to 0.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Sorting coordinates.
8 p-values are <=5e-324 which LDSC/MAGMA may not be able to handle. These will be converted to 0.
Reading header.
Tabular format detected.
Reading header.
Tabular format detected.
Reading header.
Tabular format detected.
Reading header.
VCF format detected.This will be converted to a standardised table format.
Importing tabular file: /Library/Frameworks/R.framework/Versions/4.2/Resources/library/MungeSumstats/extdata/eduAttainOkbay.txt
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Computing Z-score from P using formula: `sign(BETA)*sqrt(stats::qchisq(P,1,lower=FALSE)`


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77845b2b8e65.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778418f1ebf
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	EAF	Beta	SE	Pval	CHR_BP_A2_A1	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Summary statistics file does not have obvious CHR/BP columns. Checking to see if they are joined in another column.
Column CHR_BP_A2_A1 has been separated into the columns CHR, BP, A2, A1
Standardising column headers.
First line of summary statistics file: 
SNP	FRQ	BETA	SE	P	CHR	BP	A2	A1	
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77845b2b8e65.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77843fff2b56.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778418f1ebf
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77843fff2b56.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77844b12f9f4.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784690701fa
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	EAF	Beta	SE	Pval	CHR_BP_A2_A1	CHR_BP_A2_A1_2	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Summary statistics file does not have obvious CHR/BP columns. Checking to see if they are joined in another column.
Warning: Multiple columns in the sumstats file seem to relate to Chromosome:Base Pair position:A2:A1.
The column CHR_BP_A2_A1_2 will be kept whereas the column(s) CHR_BP_A2_A1 will be removed.
If this is not the correct column to keep, please remove all incorrect columns from those listed here before 
running `format_sumstats()`.
Column CHR_BP_A2_A1_2 has been separated into the columns CHR, BP, A2, A1
Standardising column headers.
First line of summary statistics file: 
SNP	FRQ	BETA	SE	P	CHR	BP	A2	A1	
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77844b12f9f4.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77847bf4641c.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784690701fa
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77847bf4641c.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77845d324ff3.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784481cd631
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	EAF	Beta	SE	Pval	alleles	allele	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Warning: Multiple columns in the sumstats file seem to relate to alleles A1>A2.
The column ALLELES will be kept whereas the column(s) ALLELE will be removed.
If this is not the correct column to keep, please remove all incorrect columns from those listed here before 
running `format_sumstats()`.
Column ALLELES has been separated into the columns A1, A2
Checking A1 is uppercase
Checking A2 is uppercase
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77845d324ff3.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778450eda6bf.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784481cd631
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778450eda6bf.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77843073a408.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77845a8c4a91
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	A1	A2	EAF	Beta	SE	Pval	CHR_BP	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Summary statistics file does not have obvious CHR/BP columns. Checking to see if they are joined in another column.
Column CHR_BP has been separated into the columns CHR, BP
Standardising column headers.
First line of summary statistics file: 
SNP	A1	A2	FRQ	BETA	SE	P	CHR	BP	
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77843073a408.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77846cfe5d06.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77845a8c4a91
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77846cfe5d06.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77841a017009.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778487678fe
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	A1	A2	EAF	Beta	SE	Pval	CHR_BP	CHR_BP_2	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Summary statistics file does not have obvious CHR/BP columns. Checking to see if they are joined in another column.
Warning: Multiple columns in the sumstats file seem to relate to Chromosome:Base Pair position.
The column CHR_BP_2 will be kept whereas the column(s) CHR_BP will be removed.
If this is not the correct column to keep, please remove all incorrect columns from those listed here before 
running `format_sumstats()`.
Column CHR_BP_2 has been separated into the columns CHR, BP
Standardising column headers.
First line of summary statistics file: 
SNP	A1	A2	FRQ	BETA	SE	P	CHR	BP	
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77841a017009.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778424c1b7ec.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778487678fe
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778424c1b7ec.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77842ebbb52c.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778418cec455
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77842ebbb52c.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77846fb20ad9.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778420ee191a
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77846fb20ad9.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.
Setting sorted=FALSE (required when formatted=FALSE).
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Assigning N=1000 for all SNPs.
N already exists within sumstats_dt.
[1] "Testing: compute_n='ldsc'"
Computing effective sample size using the LDSC method:
 Neff = (N_CAS+N_CON) * (N_CAS/(N_CAS+N_CON)) / mean((N_CAS/(N_CAS+N_CON))[(N_CAS+N_CON)==max(N_CAS+N_CON)]))
[1] "Testing: compute_n='giant'"
Computing effective sample size using the GIANT method:
 Neff = 2 / (1/N_CAS + 1/N_CON)
[1] "Testing: compute_n='metal'"
Computing effective sample size using the METAL method:
 Neff = 4 / (1/N_CAS + 1/N_CON)
[1] "Testing: compute_n='sum'"
Computing sample size using the sum method:
 N = N_CAS + N_CON


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778469718253.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77847af8e0d7
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778469718253.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778441c6d933.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Saving output messages to:
/tmp/RtmpXFes5o/MungeSumstats_log_msg.txt
Any runtime errors will be saved to:
/tmp/RtmpXFes5o/MungeSumstats_log_output.txt
Messages will not be printed to terminal.
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77843f58ba62.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77843dc8acc5
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77843f58ba62.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778449415625.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77841d248795
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 186 rows
   - 93 unique variants
   - 140 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
93 sumstat rows are duplicated. These duplicates will be removed.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778449415625.tsv.gz
Summary statistics report:
   - 93 rows (50% of original 186 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77842a10004e.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77841d248795
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77842a10004e.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77847f4f0605.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77841d248795
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 94 rows
   - 94 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
1 base-pair positions are duplicated in the sumstats file. These duplicates will be removed.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Loading reference genome data.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77847f4f0605.tsv.gz
Summary statistics report:
   - 93 rows (98.9% of original 94 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784352c1964.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784fcc69a6
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Filtering effect columns, ensuring none equal 0.
5 SNPs have effect values = 0 and will be removed
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
44 SNPs (50%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784352c1964.tsv.gz
Summary statistics report:
   - 88 rows (94.6% of original 93 rows)
   - 88 unique variants
   - 65 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778441327b53.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77842cbf44a0
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	FRQ	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs based on FRQ.
38 SNPs are below the FRQ threshold of 0.9 and will be removed.
Writing in tabular format ==>  /tmp/RtmpXFes5o/frq_filter.tsv.gz
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
55 SNPs (100%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778441327b53.tsv.gz
Summary statistics report:
   - 55 rows (59.1% of original 93 rows)
   - 55 unique variants
   - 41 genome-wide significant variants (P<5e-8)
   - 16 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     EAF   BETA    SE         P      FRQ
1: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10 1.863269
2: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14 1.169733
3:  rs1008078   1 91189731  T  C 0.37310 -0.016 0.003 6.005e-10 1.401423
4: rs61787263   1 98618714  T  C 0.76120  0.016 0.003 5.391e-08 1.873332
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778460b04a8a.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77842cbf44a0
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	FRQ	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs based on FRQ.
38 SNPs are below the FRQ threshold of 0.9 and will be removed.
Writing in tabular format ==>  /tmp/RtmpXFes5o/frq_filter.tsv.gz
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
55 SNPs (100%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=FALSE, the FRQ column will be renamed MAJOR_ALLELE_FRQ to differentiate the values from 
minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778460b04a8a.tsv.gz
Summary statistics report:
   - 55 rows (59.1% of original 93 rows)
   - 55 unique variants
   - 41 genome-wide significant variants (P<5e-8)
   - 16 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     EAF   BETA    SE         P
1: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
2: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
3:  rs1008078   1 91189731  T  C 0.37310 -0.016 0.003 6.005e-10
4: rs61787263   1 98618714  T  C 0.76120  0.016 0.003 5.391e-08
   MAJOR_ALLELE_FRQ
1:         1.863269
2:         1.169733
3:         1.401423
4:         1.873332
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77846c9e43f2.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77841355e6b8
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	CHR	BP	A1	A2	FRQ	BETA	SE	P	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77846c9e43f2.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784740fb2c4.tsv.gz
Standardising column headers.
First line of summary statistics file: 
SNP	CHR	BP	A1	A2	Uniq.a1a2	EAF	BETA	P	
Summary statistics report:
   - 2 rows
   - 2 unique variants
   - 1 genome-wide significant variants (P<5e-8)
   - 2 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Ensuring all SNPs are on the reference genome.
Loading reference genome data.
Found 1 Indels. These won't be checked against the reference genome as it does not contain Indels.
WARNING If your sumstat doesn't contain Indels, set the indel param to FALSE & rerun MungeSumstats::format_sumstats()
Checking for correct direction of A1 (reference) and A2 (alternative allele).
There are 1 SNPs where A1 doesn't match the reference genome.
These will be flipped with their effect columns.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
Found  Indels. These won't be checked for duplicates based on base-pair position as there can be multiples.
WARNING If your sumstat doesn't contain Indels, set the indel param to FALSE & rerun MungeSumstats::format_sumstats()
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
SE is not present but can be imputed with BETA & P. Set impute_se=TRUE and rerun to do this.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Warning: When method is an integer, must be >0.
1 SNPs (50%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784740fb2c4.tsv.gz
Summary statistics report:
   - 2 rows (100% of original 2 rows)
   - 2 unique variants
   - 1 genome-wide significant variants (P<5e-8)
   - 2 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR        BP A1 A2      UNIQ.A1A2       FRQ         BETA
1: rs12987662   2 100821548  C  A             aa 0.6213000 -0.027000000
2: rs34589910   4   6364621  C CG 4:6364621_C_CG 0.0945334 -0.006257323
              P
1: 2.693000e-24
2: 4.883341e-01
Returning data directly.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77841063e88d.tsv.gz
Standardising column headers.
First line of summary statistics file: 
SNP	CHR	BP	A1	A2	Uniq.a1a2	EAF	BETA	P	
Summary statistics report:
   - 3 rows
   - 3 unique variants
   - 1 genome-wide significant variants (P<5e-8)
   - 3 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
2 SNP IDs appear to be made up of chr:bp, these will be replaced by their SNP ID from the reference genome
Found  Indels. These won't be checked against the reference genome as it does not contain Indels.
WARNING If your sumstat doesn't contain Indels, set the indel param to FALSE & rerun MungeSumstats::format_sumstats()
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Ensuring all SNPs are on the reference genome.
Loading reference genome data.
Checking for correct direction of A1 (reference) and A2 (alternative allele).
There are 2 SNPs where A1 doesn't match the reference genome.
These will be flipped with their effect columns.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
INFO column not available. Skipping INFO score filtering step.
SE is not present but can be imputed with BETA & P. Set impute_se=TRUE and rerun to do this.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Warning: When method is an integer, must be >0.
2 SNPs (100%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77841063e88d.tsv.gz
Summary statistics report:
   - 2 rows (66.7% of original 3 rows)
   - 2 unique variants
   - 1 genome-wide significant variants (P<5e-8)
   - 2 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR        BP A1 A2 UNIQ.A1A2    FRQ    BETA         P
1: rs12987662   2 100821548  C  A        aa 0.6213 -0.0270 2.693e-24
2:  rs9320913   6  98584733  C  A        bb 0.5433 -0.0123 2.100e-07
Returning data directly.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778448c3ca63.tsv
Converting full summary stats file to tabix format for fast querying...
Reading header.
Ensuring file is bgzipped.
Tabix-indexing file.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778444fa7bb9.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77843db153e3
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	INFO	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
Filtering SNPs based on INFO score.
38 SNPs are below the INFO threshold of 0.9 and will be removed.
Writing in tabular format ==>  /tmp/RtmpXFes5o/info_filter.tsv.gz
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
28 SNPs (50.9%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778444fa7bb9.tsv.gz
Summary statistics report:
   - 55 rows (59.1% of original 93 rows)
   - 55 unique variants
   - 41 genome-wide significant variants (P<5e-8)
   - 16 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P     INFO
1: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10 1.863269
2: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14 1.169733
3:  rs1008078   1 91189731  T  C 0.37310 -0.016 0.003 6.005e-10 1.401423
4: rs61787263   1 98618714  T  C 0.76120  0.016 0.003 5.391e-08 1.873332
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77844030fb32.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778467d4bea7
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77844030fb32.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778453895e7d.tsv.gz
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778453895e7d.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Sorting coordinates.
Performing data liftover from hg19 to hg38.
Downloading chain file from UCSC Genome Browser.
trying URL 'ftp://hgdownload.cse.ucsc.edu/goldenPath/hg19/liftOver/hg19ToHg38.over.chain.gz'
Content type 'unknown' length 227698 bytes (222 KB)
==================================================
/tmp/RtmpXFes5o/hg19ToHg38.over.chain.gz
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Performing data liftover from hg19 to hg38.
Using existing chain file.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778470cda435.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77843297f685
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Ensuring all SNPs are on the reference genome.
Loading reference genome data.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Performing data liftover from hg19 to hg38.
Using existing chain file.
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778470cda435.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8430543  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43516856  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72267927  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72296486  T  C 0.23690 -0.017 0.003 1.797e-08
   IMPUTATION_gen_build
1:                 TRUE
2:                 TRUE
3:                 TRUE
4:                 TRUE
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77845fc2e669.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Importing tabular file: /tmp/RtmpXFes5o/file778470cda435.tsv.gz
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	CHR	BP	A1	A2	FRQ	BETA	SE	P	IMPUTATION_gen_build	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Ensuring all SNPs are on the reference genome.
Loading reference genome data.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Performing data liftover from hg38 to hg19.
Using existing chain file.
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77845fc2e669.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
   IMPUTATION_GEN_BUILD IMPUTATION_gen_build
1:                 TRUE                 TRUE
2:                 TRUE                 TRUE
3:                 TRUE                 TRUE
4:                 TRUE                 TRUE
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77843fe72f3f.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77843297f685
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Ensuring all SNPs are on the reference genome.
Loading reference genome data.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77843fe72f3f.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.
[1] "/tmp/RtmpXFes5o/data/file1/file77846c3d3d68.tsv.gz"
[1] "/tmp/RtmpXFes5o/data/file2/file7784288aae5c.tsv.gz"
[1] "/tmp/RtmpXFes5o/data/file3/file778428bd2ecf.tsv.gz"
[1] "/tmp/RtmpXFes5o/data/file4/file77841c4c2cee.tsv.gz"
[1] "/tmp/RtmpXFes5o/data/file5/file77844d19cbc5.tsv.gz"
[1] "/tmp/RtmpXFes5o/data/file6/file778458911a0e.tsv.gz"
[1] "/tmp/RtmpXFes5o/data/file7/file77841e45ba8f.tsv.gz"
[1] "/tmp/RtmpXFes5o/data/file8/file778473db11cf.tsv.gz"
[1] "/tmp/RtmpXFes5o/data/file9/file7784336e6875.tsv.gz"
[1] "/tmp/RtmpXFes5o/data/file10/file7784158bf3b4.tsv.gz"
10 file(s) found.
Parsing info from 10 log file(s).


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77847944c2d1.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784172cb979
Checking for empty columns.
Removing 1 empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 92 unique variants
   - 69 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
WARNING: 1 rows in sumstats file are missing data and will be removed.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
46 SNPs (50%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77847944c2d1.tsv.gz
Summary statistics report:
   - 92 rows (98.9% of original 93 rows)
   - 92 unique variants
   - 69 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2    FRQ   BETA    SE         P
1: rs10061788   5 87934707  A  G 0.2164  0.021 0.004 2.464e-09
2:  rs1007883  16 51163406  T  C 0.3713 -0.015 0.003 5.326e-08
3:  rs1008078   1 91189731  T  C 0.3731 -0.016 0.003 6.005e-10
4:  rs1043209  14 23373986  A  G 0.6026  0.018 0.003 1.816e-11
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77847d362556.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784172cb979
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77847d362556.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2    FRQ   BETA    SE         P
1: rs10061788   5 87934707  A  G 0.2164  0.021 0.004 2.464e-09
2:  rs1007883  16 51163406  T  C 0.3713 -0.015 0.003 5.326e-08
3:  rs1008078   1 91189731  T  C 0.3731 -0.016 0.003 6.005e-10
4:  rs1043209  14 23373986  A  G 0.6026  0.018 0.003 1.816e-11
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784a5ad5bf.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77845311b665
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
1 SNPs found with multiple RSIDs on one row, the first will be taken. If you would rather remove these SNPs set
`remove_multi_rs_snp=TRUE`.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784a5ad5bf.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
   convert_multi_rs_SNP
1:                   NA
2:                   NA
3:                   NA
4:                   NA
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784466c0047.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77845311b665
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784466c0047.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77841fabcba.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77842fddcb7e
Checking for empty columns.
Removing 1 empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 92 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Writing in tabular format ==>  /tmp/RtmpXFes5o/snp_multi_rs_one_row.tsv.gz
1 SNPs found with multiple RSIDs on one row, these will be removed. If you would rather take the first RS ID set
`remove_multi_rs_snp`=FALSE
Checking SNP RSIDs.
1 SNP IDs are not correctly formatted. These will be corrected from the reference genome.
Writing in tabular format ==>  /tmp/RtmpXFes5o/snp_not_found_from_chr_bp.tsv.gz
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Ensuring all SNPs are on the reference genome.
Loading reference genome data.
1 SNPs are not on the reference genome. These will be corrected from the reference genome.
Writing in tabular format ==>  /tmp/RtmpXFes5o/snp_not_found_from_chr_bp_2.tsv.gz
Loading reference genome data.
Checking for correct direction of A1 (reference) and A2 (alternative allele).
There are 43 SNPs where A1 doesn't match the reference genome.
These will be flipped with their effect columns.
Checking for missing data.
WARNING: 1 rows in sumstats file are missing data and will be removed.
Writing in tabular format ==>  /tmp/RtmpXFes5o/missing_data.tsv.gz
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
1 RSIDs are duplicated in the sumstats file. These duplicates will be removed
Writing in tabular format ==>  /tmp/RtmpXFes5o/dup_snp_id.tsv.gz
Checking for SNPs with duplicated base-pair positions.
1 base-pair positions are duplicated in the sumstats file. These duplicates will be removed.
Writing in tabular format ==>  /tmp/RtmpXFes5o/dup_base_pair_position.tsv.gz
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
1 SNPs have SE values <= 0 and will be removed
Writing in tabular format ==>  /tmp/RtmpXFes5o/se_neg.tsv.gz
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for strand ambiguous SNPs.
8 SNPs are strand-ambiguous alleles including 4 A/T and 4 C/G ambiguous SNPs. These will be removed
Writing in tabular format ==>  /tmp/RtmpXFes5o/snp_strand_ambiguous.tsv.gz
Checking for bi-allelic SNPs.
Warning: When method is an integer, must be >0.
54 SNPs (68.4%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77841fabcba.tsv.gz
Summary statistics report:
   - 79 rows (84.9% of original 93 rows)
   - 79 unique variants
   - 57 genome-wide significant variants (P<5e-8)
   - 18 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P IMPUTATION_SNP
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08             NA
2: rs34305371   1 72733610  G  A 0.91231 -0.035 0.005 3.762e-14             NA
3:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08             NA
4:  rs1008078   1 91189731  C  T 0.62690  0.016 0.003 6.005e-10             NA
   flipped
1:      NA
2:    TRUE
3:      NA
4:    TRUE
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77843099c752.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778436dc2b39
Checking for empty columns.
Removing 1 empty columns.
Standardising column headers.
First line of summary statistics file: 
chromosome	rs_id	markername	position_hg18	Effect_allele	Other_allele	EAF_HapMapCEU	N_SMK	Effect_SMK	StdErr_SMK	P_value_SMK	N_NONSMK	Effect_NonSMK	StdErr_NonSMK	P_value_NonSMK	
Summary statistics report:
   - 5 rows
   - 5 unique variants
   - 1 chromosomes
Checking for multi-GWAS.
WARNING: Multiple traits found in sumstats file only one of which can be analysed: 
SMK, NONSMK
Standardising column headers.
First line of summary statistics file: 
CHR	SNP	MARKERNAME	POSITION_HG18	A2	A1	EAF_HAPMAPCEU	N	EFFECT	STDERR	P_VALUE	N_NONSMK	EFFECT_NONSMK	STDERR_NONSMK	P_VALUE_NONSMK	
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
1 SNP IDs are not correctly formatted and will be removed.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Summary statistics file does not have obvious CHR/BP columns. Checking to see if they are joined in another column.
Column MARKERNAME has been separated into the columns CHR, BP
Standardising column headers.
First line of summary statistics file: 
CHR	SNP	POSITION_HG18	A2	A1	EAF_HAPMAPCEU	N	BETA	SE	P	N_NONSMK	EFFECT_NONSMK	STDERR_NONSMK	P_VALUE_NONSMK	BP	
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Ensuring that the N column is all integers.
The sumstats N column is not all integers, this could effect downstream analysis. These will be converted to integers.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Making X/Y CHR uppercase.
N already exists within sumstats_dt.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77843099c752.tsv.gz
Summary statistics report:
   - 4 rows (80% of original 5 rows)
   - 4 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
         SNP  CHR        BP A1 A2 POSITION_HG18 EAF_HAPMAPCEU     N    BETA
1: rs1000050 chr1 161003087  C  T     161003087        0.9000 36257  0.0001
2: rs1000073 chr1 155522020  G  A     155522020        0.3136 36335  0.0046
3: rs1000075 chr1  94939420  C  T      94939420        0.3583 38959 -0.0013
4: rs1000085 chr1  66630503  G  C      66630503        0.1667 38761  0.0053
       SE      P N_NONSMK EFFECT_NONSMK STDERR_NONSMK P_VALUE_NONSMK
1: 0.0109 0.9931   127514        0.0058        0.0059         0.3307
2: 0.0083 0.5812   126780        0.0038        0.0045         0.3979
3: 0.0082 0.8687   147567       -0.0043        0.0044         0.3259
4: 0.0095 0.5746   147259       -0.0034        0.0052         0.5157
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778445d6f7d7.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784649c1f7b
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	N	N_fixed	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Ensuring that the N column is all integers.
The sumstats N column is not all integers, this could effect downstream analysis. These will be converted to integers.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
N already exists within sumstats_dt.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778445d6f7d7.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P N N_FIXED
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08 5       5
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10 1       1
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14 1       1
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08 7       7
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778476bcdce1.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784f567b5c
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	N	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
The sumstats N column is not all integers, this could effect downstream analysis.These will NOT be converted to integers.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
1 SNPs have N values 5 standard deviations above the mean and will be removed
Writing in tabular format ==>  /tmp/RtmpXFes5o/n_large.tsv.gz
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
N already exists within sumstats_dt.
47 SNPs (51.1%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778476bcdce1.tsv.gz
Summary statistics report:
   - 92 rows (98.9% of original 93 rows)
   - 92 unique variants
   - 69 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P N
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08 3
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10 5
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14 3
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08 3
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784dda2e15.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784f567b5c
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	N	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
The sumstats N column is not all integers, this could effect downstream analysis.These will NOT be converted to integers.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
1 SNPs have N values 5 standard deviations above the mean and will be removed
Writing in tabular format ==>  /tmp/RtmpXFes5o/n_large.tsv.gz
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
N already exists within sumstats_dt.
47 SNPs (51.1%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784dda2e15.tsv.gz
Summary statistics report:
   - 92 rows (98.9% of original 93 rows)
   - 92 unique variants
   - 69 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P N
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08 3
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10 5
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14 3
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08 3
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77841ab65bdc.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784f567b5c
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	N	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
The sumstats N column is not all integers, this could effect downstream analysis.These will NOT be converted to integers.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
1 SNPs have N values 5 standard deviations above the mean and will be removed
Writing in tabular format ==>  /tmp/RtmpXFes5o/n_large.tsv.gz
Removing rows where is.na(N)
0 SNPs have N values that are NA and will be removed.
Writing in tabular format ==>  /tmp/RtmpXFes5o/n_null.tsv.gz
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
N already exists within sumstats_dt.
47 SNPs (51.1%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77841ab65bdc.tsv.gz
Summary statistics report:
   - 92 rows (98.9% of original 93 rows)
   - 92 unique variants
   - 69 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P N
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08 3
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10 5
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14 3
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08 3
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778410183256.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784255f3edd
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
WARNING: No A2 column found in the data, multi-allelic can't not be accurately chosen (as any
of the choices could be valid). bi_allelic_filter has been forced to TRUE.
Loading reference genome data.
There is no A1 or A2 allele information column found within the data. It must be inferred from other column information.
Deriving both A1 and A2 from reference genome
WARNING: Inferring the alternative allele (A2) from the reference genome. In some instances, there are more than one
alternative allele. Arbitrarily, only the first will be kept. See column `alt_alleles` in your returned sumstats file
for all alternative alleles.
Writing in tabular format ==>  /tmp/RtmpXFes5o/alleles_not_found_from_snp.tsv.gz
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778410183256.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P alt_alleles
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08           C
2: rs11210860   1 43982527  G  A 0.36940  0.017 0.003 2.359e-10           A
3: rs34305371   1 72733610  G  A 0.08769  0.035 0.005 3.762e-14           A
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08           C
   IMPUTATION_A1 IMPUTATION_A2
1:          TRUE          TRUE
2:          TRUE          TRUE
3:          TRUE          TRUE
4:          TRUE          TRUE
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784c601d4.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784255f3edd
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A2 is uppercase
Loading reference genome data.
There is no A1 or A2 allele information column found within the data. It must be inferred from other column information.
One of A1/A2 are missing, allele flipping will be tested
Deriving A1 from reference genome
Writing in tabular format ==>  /tmp/RtmpXFes5o/alleles_not_found_from_snp.tsv.gz
Checking for correct direction of A1 (reference) and A2 (alternative allele).
There are 46 SNPs where A1 doesn't match the reference genome.
These will be flipped with their effect columns.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784c601d4.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P IMPUTATION_A1
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08          TRUE
2: rs11210860   1 43982527  G  G 0.36940 -0.017 0.003 2.359e-10          TRUE
3: rs34305371   1 72733610  G  G 0.08769 -0.035 0.005 3.762e-14          TRUE
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08          TRUE
   flipped
1:      NA
2:    TRUE
3:    TRUE
4:      NA
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77847d42738e.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784255f3edd
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
WARNING: No A2 column found in the data, multi-allelic can't not be accurately chosen (as any
of the choices could be valid). bi_allelic_filter has been forced to TRUE.
Loading reference genome data.
There is no A1 or A2 allele information column found within the data. It must be inferred from other column information.
One of A1/A2 are missing, allele flipping will be tested
Deriving A2 from reference genome
WARNING: Inferring the alternative allele (A2) from the reference genome. In some instances, there are more than one
alternative allele. Arbitrarily, only the first will be kept. See column `alt_alleles` in your returned sumstats file
for all alternative alleles.
Writing in tabular format ==>  /tmp/RtmpXFes5o/alleles_not_found_from_snp.tsv.gz
Checking for correct direction of A1 (reference) and A2 (alternative allele).
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77847d42738e.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P alt_alleles
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08           C
2: rs11210860   1 43982527  A  A 0.36940  0.017 0.003 2.359e-10           A
3: rs34305371   1 72733610  A  A 0.08769  0.035 0.005 3.762e-14           A
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08           C
   IMPUTATION_A2
1:          TRUE
2:          TRUE
3:          TRUE
4:          TRUE
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778427d4d19c.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784255f3edd
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for correct direction of A1 (reference) and A2 (alternative allele).
Loading reference genome data.
There are 46 SNPs where A1 doesn't match the reference genome.
These will be flipped with their effect columns.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778427d4d19c.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  G  A 0.36940 -0.017 0.003 2.359e-10
3: rs34305371   1 72733610  G  A 0.08769 -0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778441cb778.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778469c11836
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Summary statistics file does not have obvious CHR/BP columns. Checking to see if they are joined in another column.
Standardising column headers.
First line of summary statistics file: 
SNP	BP	A1	A2	FRQ	BETA	SE	P	
Loading reference genome data.
There is no Chromosome or Base Pair Position column found within the data. It must be inferred from other column information.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778441cb778.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784813e807.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77844b88e38f
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Summary statistics file does not have obvious CHR/BP columns. Checking to see if they are joined in another column.
Standardising column headers.
First line of summary statistics file: 
SNP	A1	A2	FRQ	BETA	SE	P	
Loading reference genome data.
There is no Chromosome or Base Pair Position column found within the data. It must be inferred from other column information.
Writing in tabular format ==>  /tmp/RtmpXFes5o/chr_bp_not_found_from_snp.tsv.gz
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784813e807.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778424a74a15.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784e03f093
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
1 SNP IDs are not correctly formatted. These will be corrected from the reference genome.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778424a74a15.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77846848f807.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784e03f093
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77846848f807.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778447374764.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784284c511a
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
1 SNP IDs appear to be made up of chr:bp, these will be replaced by their SNP ID from the reference genome
1 SNP IDs are not correctly formatted and will be removed.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Summary statistics file does not have obvious CHR/BP columns. Checking to see if they are joined in another column.
Standardising column headers.
First line of summary statistics file: 
SNP	A1	A2	FRQ	BETA	SE	P	
Loading reference genome data.
There is no Chromosome or Base Pair Position column found within the data. It must be inferred from other column information.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
46 SNPs (50%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778447374764.tsv.gz
Summary statistics report:
   - 92 rows (98.9% of original 93 rows)
   - 92 unique variants
   - 69 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77848b635b.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77842a6096a1
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
1 SNP IDs are not correctly formatted. These will be corrected from the reference genome.
1 SNP IDs appear to be made up of chr:bp, these will be replaced by their SNP ID from the reference genome
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77848b635b.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77845985dd7d.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77842b4139c3
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77841d786564.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784284c511a
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77841d786564.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784577abd09.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77847a29f0b7
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
There is no SNP column found within the data. It must be inferred from other column information.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784577abd09.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778476dcdf5a.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77844fb50adf
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Ensuring all SNPs are on the reference genome.
Loading reference genome data.
1 SNPs are not on the reference genome. These will be corrected from the reference genome.
Writing in tabular format ==>  /tmp/RtmpXFes5o/snp_not_found_from_chr_bp.tsv.gz
Loading reference genome data.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778476dcdf5a.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77846a700317.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77844fb50adf
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Ensuring all SNPs are on the reference genome.
Loading reference genome data.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77846a700317.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.
Inferring genome build of 1 sumstats file(s).
ss1
Inferring genome build.
Reading in only the first 50 rows of sumstats.
Importing tabular file: /Library/Frameworks/R.framework/Versions/4.2/Resources/library/MungeSumstats/extdata/eduAttainOkbay.txt
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Loading reference genome data.
Loading reference genome data.
Inferred genome build: GRCH37
Time difference of 1.168768 mins
GRCH37: 1 file(s)


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77844c99e3ae.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778420e3d0b0
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 23 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
3 SNPs are on chromosomes X, Y, MT and will be removed
Writing in tabular format ==>  /tmp/RtmpXFes5o/chr_excl.tsv.gz
Warning: When method is an integer, must be >0.
45 SNPs (50%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77844c99e3ae.tsv.gz
Summary statistics report:
   - 90 rows (96.8% of original 93 rows)
   - 90 unique variants
   - 67 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784eae3cb5.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778420e3d0b0
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784eae3cb5.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778452f5cfe2
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	CHR	BP	A1	A2	FRQ	BETA	SE	P	
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77843c577ae9
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	CHR	BP	A1	A2	FRQ	BETA	SE	P	
Sorting coordinates.
Writing in VCF format ==>  /tmp/RtmpXFes5o/file778476e96cc0.vcf.gz
Converting summary statistics to Genomic Ranges.
Converting summary statistics to VRanges.
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 1 empty columns.
Time difference of 0.4 secs
7 empty column(s) detected.
1 sample detected: GWAS
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 2.1 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 3 empty columns.
Time difference of 0.3 secs
Checking for empty columns.
No INFO (SI) column detected.
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
ID	chr	BP	end	REF	ALT	SNP	FRQ	BETA	SE	P	
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.4 secs
6 empty column(s) detected.
1 sample detected: EBI-a-GCST005647
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 2.6 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.3 secs
Dropping 2 duplicate columns.
Checking for empty columns.
Unlisting 4 columns.
Renaming ID as SNP.
VCF file has -log10 P-values, these will be  converted to unadjusted p-values in the 'P' column.
No INFO (SI) column detected.
Standardising column headers.
First line of summary statistics file: 
SNP	chr	BP	end	REF	ALT	FILTER	AF	ES	LP	SE	P	
Sorting coordinates.
Writing in VCF format ==>  /tmp/RtmpXFes5o/file7784daece28.vcf.gz
Converting summary statistics to Genomic Ranges.
Converting summary statistics to VRanges.
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 3 empty columns.
Time difference of 0.5 secs
6 empty column(s) detected.
1 sample detected: GWAS
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 2 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 3 empty columns.
Time difference of 0.3 secs
Checking for empty columns.
VCF file has -log10 P-values, these will be  converted to unadjusted p-values in the 'P' column.
No INFO (SI) column detected.
Standardising column headers.
First line of summary statistics file: 
ID	chr	BP	end	REF	ALT	SNP	END	FILTER	FRQ	BETA	LP	SE	P	


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784515765e.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Standardising column headers.
First line of summary statistics file: 
SNP	P	FRQ	BETA	CHR	BP	
Summary statistics report:
   - 5 rows
   - 5 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
5 SNP IDs contain other information in the same column. These will be separated.
Checking for merged allele column.
Column SNP_INFO has been separated into the columns A1, A2
Checking A1 is uppercase
Checking A2 is uppercase
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
SE is not present but can be imputed with BETA & P. Set impute_se=TRUE and rerun to do this.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
3 SNPs (60%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784515765e.tsv.gz
Summary statistics report:
   - 5 rows (100% of original 5 rows)
   - 5 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
           SNP CHR    BP A1 A2           P       FRQ      BETA
1: rs140052487   1 54353  C  A 0.037219838 0.3000548 0.8797957
2: rs558796213   1 54564  G  T 0.004382482 0.5848666 0.7068747
3: rs561234294   1 54591  A  G 0.070968402 0.3334671 0.7319726
4:   rs2462492   1 54676  C  T 0.065769040 0.6220120 0.9316344
Returning data directly.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

******::NOTE::******
 - Log results will be saved to `tempdir()` by default.
 - This means all log data from the run will be  deleted upon ending the R session.
 - To keep it, change `log_folder` to an actual directory  (e.g. log_folder='./').
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77847944eb82.tsv.gz
Log data to be saved to ==>  /tmp/RtmpXFes5o
Standardising column headers.
First line of summary statistics file: 
SNP	P	FRQ	BETA	CHR	BP	A1	A2	
Summary statistics report:
   - 5 rows
   - 5 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
SE is not present but can be imputed with BETA & P. Set impute_se=TRUE and rerun to do this.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
3 SNPs (60%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77847944eb82.tsv.gz
Summary statistics report:
   - 5 rows (100% of original 5 rows)
   - 5 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
           SNP CHR    BP A1 A2           P       FRQ      BETA
1: rs140052487   1 54353  C  A 0.037219838 0.3000548 0.8797957
2: rs558796213   1 54564  G  T 0.004382482 0.5848666 0.7068747
3: rs561234294   1 54591  A  G 0.070968402 0.3334671 0.7319726
4:   rs2462492   1 54676  C  T 0.065769040 0.6220120 0.9316344
Returning data directly.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784f36ae1f.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778455dcbde3
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778445fe4396.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778435d73d5f
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778445fe4396.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77846f0d34df.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778435d73d5f
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77846f0d34df.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784713f2fc5.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77844109e786
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784713f2fc5.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77844b796a71.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file77842bfc754e
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
47 SNPs (50.5%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77844b796a71.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778478735bf.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784453e754d
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
5 SNPs have SE values <= 0 and will be removed
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
44 SNPs (50%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778478735bf.tsv.gz
Summary statistics report:
   - 88 rows (94.6% of original 93 rows)
   - 88 unique variants
   - 65 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	Support	
Returning unmapped column names without making them uppercase.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	Support	
Returning unmapped column names without making them uppercase.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77847c025b1a.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778460faf55b
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 85 rows
   - 85 unique variants
   - 63 genome-wide significant variants (P<5e-8)
   - 19 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for strand ambiguous SNPs.
Warning: When method is an integer, must be >0.
43 SNPs (50.6%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77847c025b1a.tsv.gz
Summary statistics report:
   - 85 rows (100% of original 85 rows)
   - 85 unique variants
   - 63 genome-wide significant variants (P<5e-8)
   - 19 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784707e6831.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file778460faf55b
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for strand ambiguous SNPs.
8 SNPs are strand-ambiguous alleles including 4 A/T and 4 C/G ambiguous SNPs. These will be removed
Warning: When method is an integer, must be >0.
43 SNPs (50.6%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784707e6831.tsv.gz
Summary statistics report:
   - 85 rows (91.4% of original 93 rows)
   - 85 unique variants
   - 63 genome-wide significant variants (P<5e-8)
   - 19 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     FRQ   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778459dcc8b0.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77842dfbc8e7.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784792e784f
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77842dfbc8e7.tsv.gz
Summary statistics report:
   - 93 rows (100% of original 93 rows)
   - 93 unique variants
   - 70 genome-wide significant variants (P<5e-8)
   - 20 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
          SNP CHR       BP A1 A2     EAF   BETA    SE         P
1:   rs301800   1  8490603  T  C 0.17910  0.019 0.003 1.794e-08
2: rs11210860   1 43982527  A  G 0.36940  0.017 0.003 2.359e-10
3: rs34305371   1 72733610  A  G 0.08769  0.035 0.005 3.762e-14
4:  rs2568955   1 72762169  T  C 0.23690 -0.017 0.003 1.797e-08
Returning data directly.
Converting summary statistics to Genomic Ranges.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77843f2fc558.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784594534d0.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77844e8e7179.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778469bbe739.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77842f49856a.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77843d60a67.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77845944f228.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77843d764de1.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778421f30e4d.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77845c2ff2a4.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77844fe31c44.tsv.gz


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784148f1c09.tsv.gz
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.4 secs
6 empty column(s) detected.
1 sample detected: EBI-a-GCST005647
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 2.4 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.3 secs
Dropping 2 duplicate columns.
Checking for empty columns.
Unlisting 4 columns.
Renaming ID as SNP.
VCF file has -log10 P-values, these will be  converted to unadjusted p-values in the 'P' column.
No INFO (SI) column detected.
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	chr	BP	end	REF	ALT	FILTER	AF	ES	LP	SE	P	
Summary statistics report:
   - 101 rows
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
2 SNPs (2%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784148f1c09.tsv.gz
Summary statistics report:
   - 101 rows (100% of original 101 rows)
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
           SNP CHR    BP A1 A2   END FILTER    FRQ    BETA       LP     SE
1:  rs58108140   1 10583  G  A 10583   PASS 0.1589  0.0312 0.369267 0.0393
2:    rs806731   1 30923  G  T 30923   PASS 0.7843 -0.0114 0.126854 0.0353
3: rs116400033   1 51479  T  A 51479   PASS 0.1829  0.0711 1.262410 0.0370
4: rs146477069   1 54421  A  G 54421   PASS 0.0352 -0.0240 0.112102 0.0830
            P
1: 0.42730011
2: 0.74669974
3: 0.05464998
4: 0.77249913
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784e1ca505.tsv.gz
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.4 secs
6 empty column(s) detected.
1 sample detected: EBI-a-GCST005647
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 2.4 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.3 secs
Dropping 2 duplicate columns.
Checking for empty columns.
Unlisting 4 columns.
Renaming ID as SNP.
VCF file has -log10 P-values, these will be  converted to unadjusted p-values in the 'P' column.
No INFO (SI) column detected.
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	chr	BP	end	REF	ALT	FILTER	AF	ES	LP	SE	P	
Summary statistics report:
   - 101 rows
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for correct direction of A1 (reference) and A2 (alternative allele).
Loading reference genome data.
There are 1 SNPs where A1 doesn't match the reference genome.
These will be flipped with their effect columns.
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicate SNPs from SNP ID.
Checking for SNPs with duplicated base-pair positions.
Found  Indels. These won't be checked for duplicates based on base-pair position as there can be multiples.
WARNING If your sumstat doesn't contain Indels, set the indel param to FALSE & rerun MungeSumstats::format_sumstats()
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Checking for bi-allelic SNPs.
Warning: When method is an integer, must be >0.
2 SNPs (2%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784e1ca505.tsv.gz
Summary statistics report:
   - 101 rows (100% of original 101 rows)
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
           SNP CHR    BP A1 A2   END FILTER    FRQ    BETA       LP     SE
1:  rs58108140   1 10583  G  A 10583   PASS 0.1589  0.0312 0.369267 0.0393
2:    rs806731   1 30923  G  T 30923   PASS 0.7843 -0.0114 0.126854 0.0353
3: rs116400033   1 51479  T  A 51479   PASS 0.1829  0.0711 1.262410 0.0370
4: rs146477069   1 54421  A  G 54421   PASS 0.0352 -0.0240 0.112102 0.0830
            P
1: 0.42730011
2: 0.74669974
3: 0.05464998
4: 0.77249913
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784a63aeb9.tsv.gz
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.4 secs
6 empty column(s) detected.
1 sample detected: EBI-a-GCST005647
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 2.3 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.3 secs
Dropping 2 duplicate columns.
Checking for empty columns.
Unlisting 4 columns.
Renaming ID as SNP.
VCF file has -log10 P-values, these will be  converted to unadjusted p-values in the 'P' column.
No INFO (SI) column detected.
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	chr	BP	end	REF	ALT	FILTER	AF	ES	LP	SE	P	
Summary statistics report:
   - 101 rows
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
2 SNPs (2%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784a63aeb9.tsv.gz
Summary statistics report:
   - 101 rows (100% of original 101 rows)
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
           SNP CHR    BP A1 A2   END FILTER    FRQ    BETA       LP     SE
1:  rs58108140   1 10583  G  A 10583   PASS 0.1589  0.0312 0.369267 0.0393
2:    rs806731   1 30923  G  T 30923   PASS 0.7843 -0.0114 0.126854 0.0353
3: rs116400033   1 51479  T  A 51479   PASS 0.1829  0.0711 1.262410 0.0370
4: rs146477069   1 54421  A  G 54421   PASS 0.0352 -0.0240 0.112102 0.0830
            P
1: 0.42730011
2: 0.74669974
3: 0.05464998
4: 0.77249913
Returning data directly.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77847d713f70.tsv.gz
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.4 secs
6 empty column(s) detected.
1 sample detected: EBI-a-GCST005647
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 2.4 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.3 secs
Dropping 2 duplicate columns.
Checking for empty columns.
Unlisting 4 columns.
Renaming ID as SNP.
VCF file has -log10 P-values, these will be  converted to unadjusted p-values in the 'P' column.
No INFO (SI) column detected.
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	chr	BP	end	REF	ALT	FILTER	AF	ES	LP	SE	P	
Summary statistics report:
   - 101 rows
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
2 SNPs (2%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77847d713f70.tsv.gz
Summary statistics report:
   - 101 rows (100% of original 101 rows)
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
           SNP CHR    BP A1 A2   END FILTER    FRQ    BETA       LP     SE
1:  rs58108140   1 10583  G  A 10583   PASS 0.1589  0.0312 0.369267 0.0393
2:    rs806731   1 30923  G  T 30923   PASS 0.7843 -0.0114 0.126854 0.0353
3: rs116400033   1 51479  T  A 51479   PASS 0.1829  0.0711 1.262410 0.0370
4: rs146477069   1 54421  A  G 54421   PASS 0.0352 -0.0240 0.112102 0.0830
            P
1: 0.42730011
2: 0.74669974
3: 0.05464998
4: 0.77249913
Returning data directly.
Converting summary statistics to Genomic Ranges.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file7784581c3377.tsv.gz
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.4 secs
6 empty column(s) detected.
1 sample detected: EBI-a-GCST005647
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 2.4 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.3 secs
Dropping 2 duplicate columns.
Checking for empty columns.
Unlisting 4 columns.
Renaming ID as SNP.
VCF file has -log10 P-values, these will be  converted to unadjusted p-values in the 'P' column.
No INFO (SI) column detected.
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	chr	BP	end	REF	ALT	FILTER	AF	ES	LP	SE	P	
Summary statistics report:
   - 101 rows
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Warning: When method is an integer, must be >0.
2 SNPs (2%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file7784581c3377.tsv.gz
Summary statistics report:
   - 101 rows (100% of original 101 rows)
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
           SNP CHR    BP A1 A2   END FILTER    FRQ    BETA       LP     SE
1:  rs58108140   1 10583  G  A 10583   PASS 0.1589  0.0312 0.369267 0.0393
2:    rs806731   1 30923  G  T 30923   PASS 0.7843 -0.0114 0.126854 0.0353
3: rs116400033   1 51479  T  A 51479   PASS 0.1829  0.0711 1.262410 0.0370
4: rs146477069   1 54421  A  G 54421   PASS 0.0352 -0.0240 0.112102 0.0830
            P
1: 0.42730011
2: 0.74669974
3: 0.05464998
4: 0.77249913
Returning data directly.
Converting summary statistics to Genomic Ranges.
Converting summary statistics to VRanges.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77845746672e.tsv.gz
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.4 secs
6 empty column(s) detected.
1 sample detected: EBI-a-GCST005647
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 2.4 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 2 empty columns.
Time difference of 0.3 secs
Dropping 2 duplicate columns.
Checking for empty columns.
Unlisting 4 columns.
Renaming ID as SNP.
VCF file has -log10 P-values, these will be  converted to unadjusted p-values in the 'P' column.
No INFO (SI) column detected.
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
SNP	chr	BP	end	REF	ALT	FILTER	AF	ES	LP	SE	P	
Ensuring parameters comply with LDSC format.

Setting `compute_z=TRUE` to comply with LDSC format.
Summary statistics report:
   - 101 rows
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Checking for correct direction of A1 (reference) and A2 (alternative allele).
Loading reference genome data.
Reordering so first three column headers are SNP, CHR and BP in this order.
Reordering so the fourth and fifth columns are A1 and A2.
Checking for missing data.
Checking for duplicate columns.
Checking for duplicated rows.
INFO column not available. Skipping INFO score filtering step.
Filtering SNPs, ensuring SE>0.
Ensuring all SNPs have N<5 std dev above mean.
Removing 'chr' prefix from CHR.
Making X/Y CHR uppercase.
Computing Z-score from P using formula: `sign(BETA)*sqrt(stats::qchisq(P,1,lower=FALSE)`
Assigning N=1001 for all SNPs.
2 SNPs (2%) have FRQ values > 0.5. Conventionally the FRQ column is intended to show the minor/effect allele frequency.
The FRQ column was mapped from one of the following from the inputted  summary statistics file:
FRQ, EAF, FREQUENCY, FRQ_U, F_U, MAF, FREQ, FREQ_TESTED_ALLELE, FRQ_TESTED_ALLELE, FREQ_EFFECT_ALLELE, FRQ_EFFECT_ALLELE, EFFECT_ALLELE_FREQUENCY, EFFECT_ALLELE_FREQ, EFFECT_ALLELE_FRQ, A1FREQ, A1FRQ, A2FREQ, A2FRQ, ALLELE_FREQUENCY, ALLELE_FREQ, ALLELE_FRQ, AF, MINOR_AF, EFFECT_AF, A2_AF, EFF_AF, ALT_AF, ALTERNATIVE_AF, INC_AF, A_2_AF, TESTED_AF, AF1, ALLELEFREQ, ALT_FREQ, EAF_HRC, EFFECTALLELEFREQ, FREQ.A1.1000G.EUR, FREQ.A1.ESP.EUR, FREQ.ALLELE1.HAPMAPCEU, FREQ.B, FREQ1, FREQ1.HAPMAP, FREQ_EUROPEAN_1000GENOMES, FREQ_HAPMAP, FREQ_TESTED_ALLELE_IN_HRS, FRQ_A1, FRQ_U_113154, FRQ_U_31358, FRQ_U_344901, FRQ_U_43456, POOLED_ALT_AF
As frq_is_maf=TRUE, the FRQ column will not be renamed. If the FRQ values were intended to represent major allele frequency,
set frq_is_maf=FALSE to rename the column as MAJOR_ALLELE_FRQ and differentiate it from minor/effect allele frequency.
Could not recognize genome build of:
 - target_genome
These will be inferred from the data.
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77845746672e.tsv.gz
Summary statistics report:
   - 101 rows (100% of original 101 rows)
   - 101 unique variants
   - 0 genome-wide significant variants (P<5e-8)
   - 1 chromosomes
Successfully finished preparing sumstats file, preview:
Reading header.
           SNP CHR    BP A1 A2   END FILTER    FRQ    BETA       LP     SE
1:  rs58108140   1 10583  G  A 10583   PASS 0.1589  0.0312 0.369267 0.0393
2:    rs806731   1 30923  G  T 30923   PASS 0.7843 -0.0114 0.126854 0.0353
3: rs116400033   1 51479  T  A 51479   PASS 0.1829  0.0711 1.262410 0.0370
4: rs146477069   1 54421  A  G 54421   PASS 0.0352 -0.0240 0.112102 0.0830
            P          Z    N
1: 0.42730011  0.7938202 1001
2: 0.74669974 -0.3229941 1001
3: 0.05464998  1.9216487 1001
4: 0.77249913 -0.2891075 1001
Returning path to saved data.


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77844ca3a9cb.tsv.gz
Reading header.
Tabular format detected.
Importing tabular file: /tmp/RtmpXFes5o/file7784290ddafb
Checking for empty columns.
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	
Summary statistics report:
   - 93 rows
   - 93 unique variants
   - 20 chromosomes
Checking for multi-GWAS.
Checking for multiple RSIDs on one row.
Checking SNP RSIDs.
Checking for merged allele column.
Checking A1 is uppercase
Checking A2 is uppercase
Standardising column headers.
First line of summary statistics file: 
MarkerName	CHR	POS	A1	A2	EAF	Beta	SE	Pval	
Sorting coordinates.
.tsv
=== write tests ===
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77846451903e.tsv

=== read tests ===
Importing tabular file: /tmp/RtmpXFes5o/file77846451903e.tsv
Checking for empty columns.
.tsv.gz
=== write tests ===
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778426d509e6.tsv.gz

=== read tests ===
Importing tabular file: /tmp/RtmpXFes5o/file778426d509e6.tsv.gz
Checking for empty columns.
.tsv.bgz
=== write tests ===
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778413f8b348.tsv.bgz

=== read tests ===
Importing tabular bgz file: /tmp/RtmpXFes5o/file778413f8b348.tsv.bgz
Checking for empty columns.
.tsv.gz
=== write tests ===
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778468f9a2f.tsv.gz
Converting full summary stats file to tabix format for fast querying...
Reading header.
Ensuring file is bgzipped.
Tabix-indexing file.

=== read tests ===
Importing tabular bgz file: /tmp/RtmpXFes5o/file778468f9a2f.tsv.bgz
Checking for empty columns.
.tsv.bgz
=== write tests ===
Sorting coordinates.
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778467df63a4.tsv.bgz
Converting full summary stats file to tabix format for fast querying...
Reading header.
Ensuring file is bgzipped.
Tabix-indexing file.

=== read tests ===
Importing tabular bgz file: /tmp/RtmpXFes5o/file778467df63a4.tsv.bgz
Checking for empty columns.
.csv
=== write tests ===
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77842c063e64.csv

=== read tests ===
Importing tabular file: /tmp/RtmpXFes5o/file77842c063e64.csv
Checking for empty columns.
.csv.gz
=== write tests ===
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77844dea2dd0.csv.gz

=== read tests ===
Importing tabular file: /tmp/RtmpXFes5o/file77844dea2dd0.csv.gz
Checking for empty columns.
.vcf
=== write tests ===


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

save_path suggests VCF output but write_vcf=FALSE. Switching output to tabular format (.tsv.gz).
Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file778425fd9f50.tsv.gz
Writing in tabular format ==>  /tmp/RtmpXFes5o/file778425fd9f50.tsv.gz

=== read tests ===
Importing tabular file: /tmp/RtmpXFes5o/file778425fd9f50.tsv.gz
Checking for empty columns.
.vcf.gz
=== write tests ===


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

save_path suggests VCF output but write_vcf=FALSE. Switching output to tabular format (.tsv.gz).
Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77846a3a94d0.tsv.gz
Writing in tabular format ==>  /tmp/RtmpXFes5o/file77846a3a94d0.tsv.gz

=== read tests ===
Importing tabular file: /tmp/RtmpXFes5o/file77846a3a94d0.tsv.gz
Checking for empty columns.
.vcf
=== write tests ===
Sorting coordinates.
Writing in VCF format ==>  /tmp/RtmpXFes5o/file77844688a367.vcf
Converting summary statistics to Genomic Ranges.
Converting summary statistics to VRanges.

=== read tests ===
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 1 empty columns.
Time difference of 0.4 secs
7 empty column(s) detected.
1 sample detected: GWAS
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 2.2 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 3 empty columns.
Time difference of 0.3 secs
Checking for empty columns.
No INFO (SI) column detected.
Checking for empty columns.
.vcf.gz
=== write tests ===
Sorting coordinates.
Writing in VCF format ==>  /tmp/RtmpXFes5o/file7784349fe35e.vcf.gz
Converting summary statistics to Genomic Ranges.
Converting summary statistics to VRanges.

=== read tests ===
Compressing and tabix-indexing VCF file.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 1 empty columns.
Time difference of 0.4 secs
7 empty column(s) detected.
1 sample detected: GWAS
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 1.9 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 3 empty columns.
Time difference of 0.3 secs
Checking for empty columns.
No INFO (SI) column detected.
Checking for empty columns.
.vcf
=== write tests ===
Sorting coordinates.
Writing in VCF format ==>  /tmp/RtmpXFes5o/file7784467c978a.vcf
Converting summary statistics to Genomic Ranges.
Converting summary statistics to VRanges.
.vcf
=== write tests ===


******::NOTE::******
 - Formatted results will be saved to `tempdir()` by default.
 - This means all formatted summary stats will be deleted upon ending the R session.
 - To keep formatted summary stats, change `save_path`  ( e.g. `save_path=file.path('./formatted',basename(path))` ),   or make sure to copy files elsewhere after processing  ( e.g. `file.copy(save_path, './formatted/' )`.
 ******************** 

Formatted summary statistics will be saved to ==>  /tmp/RtmpXFes5o/file77841dc1092d.vcf.bgz
Sorting coordinates.
Writing in VCF format ==>  /tmp/RtmpXFes5o/file77841dc1092d.vcf.bgz
Converting summary statistics to Genomic Ranges.
Converting summary statistics to VRanges.

=== read tests ===
File already tabix-indexed.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 1 empty columns.
Time difference of 0.4 secs
7 empty column(s) detected.
1 sample detected: GWAS
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 1.9 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 3 empty columns.
Time difference of 0.3 secs
Checking for empty columns.
No INFO (SI) column detected.
Checking for empty columns.
.vcf.bgz
=== write tests ===
Sorting coordinates.
Writing in VCF format ==>  /tmp/RtmpXFes5o/file77846c41789d.vcf.bgz
Converting summary statistics to Genomic Ranges.
Converting summary statistics to VRanges.

=== read tests ===
File already tabix-indexed.
Finding empty VCF columns based on first 1e+07 rows.
Converting VCF to data.table.
Checking for empty columns.
Removing 1 empty columns.
Time difference of 0.4 secs
7 empty column(s) detected.
1 sample detected: GWAS
Constructing ScanVcfParam object.
Reading VCF file.
Time difference of 1.8 secs
Converting VCF to data.table.
Checking for empty columns.
Removing 3 empty columns.
Time difference of 0.3 secs
Checking for empty columns.
No INFO (SI) column detected.
Checking for empty columns.
[ FAIL 0 | WARN 3 | SKIP 0 | PASS 175 ]

[ FAIL 0 | WARN 3 | SKIP 0 | PASS 175 ]
> 
> proc.time()
    user   system  elapsed 
 951.490   53.920 1026.256