Xiuwen Zheng
| Snapshot Date: 2024-12-19 13:00 -0500 (Thu, 19 Dec 2024) |
| git_url: https://git.bioconductor.org/packages/SNPRelate |
| git_branch: RELEASE_3_20 |
| git_last_commit: 80684f3 |
| git_last_commit_date: 2024-10-29 09:54:31 -0500 (Tue, 29 Oct 2024) |
| Back to Multiple platform build/check report for BioC 3.20: simplified long |
|
This page was generated on 2024-12-23 12:05 -0500 (Mon, 23 Dec 2024).
| Hostname | OS | Arch (*) | R version | Installed pkgs |
|---|---|---|---|---|
| nebbiolo2 | Linux (Ubuntu 24.04.1 LTS) | x86_64 | 4.4.2 (2024-10-31) -- "Pile of Leaves" | 4744 |
| palomino8 | Windows Server 2022 Datacenter | x64 | 4.4.2 (2024-10-31 ucrt) -- "Pile of Leaves" | 4487 |
| merida1 | macOS 12.7.5 Monterey | x86_64 | 4.4.2 (2024-10-31) -- "Pile of Leaves" | 4515 |
| kjohnson1 | macOS 13.6.6 Ventura | arm64 | 4.4.2 (2024-10-31) -- "Pile of Leaves" | 4467 |
| Click on any hostname to see more info about the system (e.g. compilers) (*) as reported by 'uname -p', except on Windows and Mac OS X | ||||
| Package 2000/2289 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||||
| SNPRelate 1.40.0 (landing page) Xiuwen Zheng
| nebbiolo2 | Linux (Ubuntu 24.04.1 LTS) / x86_64 | OK | OK | OK | | ||||||||
| palomino8 | Windows Server 2022 Datacenter / x64 | OK | OK | OK | OK | | ||||||||
| merida1 | macOS 12.7.5 Monterey / x86_64 | OK | OK | OK | OK | | ||||||||
| kjohnson1 | macOS 13.6.6 Ventura / arm64 | OK | OK | OK | OK | | ||||||||
|
To the developers/maintainers of the SNPRelate package: - Allow up to 24 hours (and sometimes 48 hours) for your latest push to git@git.bioconductor.org:packages/SNPRelate.git to reflect on this report. See Troubleshooting Build Report for more information. - Use the following Renviron settings to reproduce errors and warnings. - If 'R CMD check' started to fail recently on the Linux builder(s) over a missing dependency, add the missing dependency to 'Suggests:' in your DESCRIPTION file. See Renviron.bioc for more information. |
| Package: SNPRelate |
| Version: 1.40.0 |
| Command: F:\biocbuild\bbs-3.20-bioc\R\bin\R.exe CMD check --no-multiarch --install=check:SNPRelate.install-out.txt --library=F:\biocbuild\bbs-3.20-bioc\R\library --no-vignettes --timings SNPRelate_1.40.0.tar.gz |
| StartedAt: 2024-12-20 06:11:02 -0500 (Fri, 20 Dec 2024) |
| EndedAt: 2024-12-20 06:13:53 -0500 (Fri, 20 Dec 2024) |
| EllapsedTime: 170.3 seconds |
| RetCode: 0 |
| Status: OK |
| CheckDir: SNPRelate.Rcheck |
| Warnings: 0 |
##############################################################################
##############################################################################
###
### Running command:
###
### F:\biocbuild\bbs-3.20-bioc\R\bin\R.exe CMD check --no-multiarch --install=check:SNPRelate.install-out.txt --library=F:\biocbuild\bbs-3.20-bioc\R\library --no-vignettes --timings SNPRelate_1.40.0.tar.gz
###
##############################################################################
##############################################################################
* using log directory 'F:/biocbuild/bbs-3.20-bioc/meat/SNPRelate.Rcheck'
* using R version 4.4.2 (2024-10-31 ucrt)
* using platform: x86_64-w64-mingw32
* R was compiled by
gcc.exe (GCC) 13.3.0
GNU Fortran (GCC) 13.3.0
* running under: Windows Server 2022 x64 (build 20348)
* using session charset: UTF-8
* using option '--no-vignettes'
* checking for file 'SNPRelate/DESCRIPTION' ... OK
* checking extension type ... Package
* this is package 'SNPRelate' version '1.40.0'
* 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 whether package 'SNPRelate' can be installed ... OK
* used C compiler: 'gcc.exe (GCC) 13.3.0'
* used C++ compiler: 'G__~1.EXE (GCC) 13.3.0'
* 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 code 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 whether startup messages can be suppressed ... 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 LazyData ... OK
* checking data for ASCII and uncompressed saves ... OK
* checking line endings in C/C++/Fortran sources/headers ... OK
* checking line endings in Makefiles ... OK
* checking compilation flags in Makevars ... OK
* checking for GNU extensions in Makefiles ... OK
* checking for portable use of $(BLAS_LIBS) and $(LAPACK_LIBS) ... OK
* checking use of PKG_*FLAGS in Makefiles ... OK
* checking compiled code ... NOTE
Note: information on .o files for x64 is not available
File 'F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/libs/x64/SNPRelate.dll':
Found '_exit', possibly from '_exit' (C)
Found 'abort', possibly from 'abort' (C), 'runtime' (Fortran)
Found 'exit', possibly from 'exit' (C), 'stop' (Fortran)
Compiled code should not call entry points which might terminate R nor
write to stdout/stderr instead of to the console, nor use Fortran I/O
nor system RNGs nor [v]sprintf. The detected symbols are linked into
the code but might come from libraries and not actually be called.
See 'Writing portable packages' in the 'Writing R Extensions' manual.
* checking files in 'vignettes' ... OK
* checking examples ... OK
* checking for unstated dependencies in 'tests' ... OK
* checking tests ...
Running 'runTests.R'
OK
* checking for unstated dependencies in vignettes ... OK
* checking package vignettes ... OK
* checking running R code from vignettes ... SKIPPED
* checking re-building of vignette outputs ... SKIPPED
* checking PDF version of manual ... OK
* DONE
Status: 1 NOTE
See
'F:/biocbuild/bbs-3.20-bioc/meat/SNPRelate.Rcheck/00check.log'
for details.
SNPRelate.Rcheck/00install.out
############################################################################## ############################################################################## ### ### Running command: ### ### F:\biocbuild\bbs-3.20-bioc\R\bin\R.exe CMD INSTALL SNPRelate ### ############################################################################## ############################################################################## * installing to library 'F:/biocbuild/bbs-3.20-bioc/R/library' * installing *source* package 'SNPRelate' ... ** using staged installation ** libs using C compiler: 'gcc.exe (GCC) 13.3.0' using C++ compiler: 'G__~1.EXE (GCC) 13.3.0' g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c ConvToGDS.cpp -o ConvToGDS.o gcc -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c R_SNPRelate.c -o R_SNPRelate.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c SNPRelate.cpp -o SNPRelate.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c ThreadPool.cpp -o ThreadPool.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c dGenGWAS.cpp -o dGenGWAS.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c dVect.cpp -o dVect.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c genBeta.cpp -o genBeta.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c genEIGMIX.cpp -o genEIGMIX.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c genFst.cpp -o genFst.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c genHWE.cpp -o genHWE.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c genIBD.cpp -o genIBD.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c genIBS.cpp -o genIBS.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c genKING.cpp -o genKING.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c genLD.cpp -o genLD.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c genPCA.cpp -o genPCA.o g++ -std=gnu++17 -I"F:/biocbuild/bbs-3.20-bioc/R/include" -DNDEBUG -DUSING_R -DUSE_FC_LEN_T -I. -I'F:/biocbuild/bbs-3.20-bioc/R/library/gdsfmt/include' -I"C:/rtools44/x86_64-w64-mingw32.static.posix/include" -O2 -Wall -mfpmath=sse -msse2 -mstackrealign -c genSlideWin.cpp -o genSlideWin.o g++ -std=gnu++17 -shared -s -static-libgcc -o SNPRelate.dll tmp.def ConvToGDS.o R_SNPRelate.o SNPRelate.o ThreadPool.o dGenGWAS.o dVect.o genBeta.o genEIGMIX.o genFst.o genHWE.o genIBD.o genIBS.o genKING.o genLD.o genPCA.o genSlideWin.o -LF:/biocbuild/bbs-3.20-bioc/R/bin/x64 -lRlapack -LF:/biocbuild/bbs-3.20-bioc/R/bin/x64 -lRblas -lgfortran -lm -lquadmath -LC:/rtools44/x86_64-w64-mingw32.static.posix/lib/x64 -LC:/rtools44/x86_64-w64-mingw32.static.posix/lib -LF:/biocbuild/bbs-3.20-bioc/R/bin/x64 -lR installing to F:/biocbuild/bbs-3.20-bioc/R/library/00LOCK-SNPRelate/00new/SNPRelate/libs/x64 ** R ** data *** moving datasets to lazyload DB ** 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 (SNPRelate)
SNPRelate.Rcheck/tests/runTests.Rout
R version 4.4.2 (2024-10-31 ucrt) -- "Pile of Leaves"
Copyright (C) 2024 The R Foundation for Statistical Computing
Platform: x86_64-w64-mingw32/x64
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.
> BiocGenerics:::testPackage("SNPRelate")
SNPRelate -- supported by Streaming SIMD Extensions 2 (SSE2)
Genetic Relationship Matrix (GRM, GCTA):
Excluding 8,088 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 1,000
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 282597
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:42 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Saving to the GDS file:
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:12:43 2024 Done.
Genetic Relationship Matrix (GRM, GCTA):
Excluding 7,088 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 2,000
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 559412
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:43 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Saving to the GDS file:
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:12:44 2024 Done.
Genetic Relationship Matrix (GRM, GCTA):
Excluding 5,288 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 3,800
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 1066957
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:44 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Saving to the GDS file:
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:12:45 2024 Done.
GRM merging:
open 'tmp1.gds' (1,000 variants)
open 'tmp2.gds' (2,000 variants)
open 'tmp3.gds' (3,800 variants)
Weight: 0.147059, 0.294118, 0.558824
Output: tmp.gds
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Genetic Relationship Matrix (GRM, GCTA):
Excluding 2,288 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 6,800
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 1908966
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:46 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:12:47 2024 Done.
Genetic Relationship Matrix (GRM, IndivBeta):
Excluding 8,088 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 1,000
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 282597
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:47 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Saving to the GDS file:
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:12:47 2024 Done.
Genetic Relationship Matrix (GRM, IndivBeta):
Excluding 7,088 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 2,000
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 559412
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:47 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Saving to the GDS file:
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:12:48 2024 Done.
Genetic Relationship Matrix (GRM, IndivBeta):
Excluding 5,288 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 3,800
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 1066957
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:48 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Saving to the GDS file:
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:12:49 2024 Done.
GRM merging:
open 'tmp1.gds' (1,000 variants)
open 'tmp2.gds' (2,000 variants)
open 'tmp3.gds' (3,800 variants)
Weight: 0.147059, 0.294118, 0.558824
Output: tmp.gds
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Writing ...
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Genetic Relationship Matrix (GRM, IndivBeta):
Excluding 2,288 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 6,800
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 1908966
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:49 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:12:49 2024 Done.
Linkage Disequilibrium (LD) estimation on genotypes:
# of samples: 279
# of SNPs: 1,000
using 1 thread
method: covariance
LD matrix: the sum of all selected genotypes (0,1,2) = 283058
Linkage Disequilibrium (LD) estimation on genotypes:
# of samples: 279
# of SNPs: 1,000
using 1 thread
method: correlation
LD matrix: the sum of all selected genotypes (0,1,2) = 283058
FUNCTION: SNPGDSFileClass
FUNCTION: SNPRelate-package
Start file conversion from PLINK BED to SNP GDS ...
BED file: "F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/plinkhapmap.bed.gz"
SNP-major mode (Sample X SNP), 45.7K
FAM file: "F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/plinkhapmap.fam.gz"
BIM file: "F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/plinkhapmap.bim.gz"
Fri Dec 20 06:12:53 2024 (store sample id, snp id, position, and chromosome)
start writing: 60 samples, 5000 SNPs ...
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:12:53 2024 Done.
Optimize the access efficiency ...
Clean up the fragments of GDS file:
open the file 'HapMap.gds' (98.1K)
# of fragments: 38
save to 'HapMap.gds.tmp'
rename 'HapMap.gds.tmp' (97.8K, reduced: 240B)
# of fragments: 18
Principal Component Analysis (PCA) on genotypes:
Excluding 203 SNPs on non-autosomes
Excluding 28 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 60
# of SNPs: 4,769
using 1 thread
# of principal components: 32
PCA: the sum of all selected genotypes (0,1,2) = 124273
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:53 2024 (internal increment: 75844)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:12:53 2024 Begin (eigenvalues and eigenvectors)
Fri Dec 20 06:12:53 2024 Done.
IBD analysis (PLINK method of moment) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
PLINK IBD: the sum of all selected genotypes (0,1,2) = 2446510
Fri Dec 20 06:12:53 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:12:54 2024 Done.
Identity-By-State (IBS) analysis on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
IBS: the sum of all selected genotypes (0,1,2) = 2446510
Fri Dec 20 06:12:54 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:12:55 2024 Done.
Linkage Disequilibrium (LD) estimation on genotypes:
# of samples: 279
# of SNPs: 200
using 1 thread
method: composite
LD matrix: the sum of all selected genotypes (0,1,2) = 55417
FUNCTION: hapmap_geno
FUNCTION: snpgdsAdmixPlot
Eigen-analysis on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
Eigen-analysis: the sum of all selected genotypes (0,1,2) = 2446510
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:55 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:12:56 2024 Begin (eigenvalues and eigenvectors)
Fri Dec 20 06:12:56 2024 Done.
FUNCTION: snpgdsAdmixProp
Eigen-analysis on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
Eigen-analysis: the sum of all selected genotypes (0,1,2) = 2446510
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:56 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:12:57 2024 Begin (eigenvalues and eigenvectors)
Fri Dec 20 06:12:57 2024 Done.
FUNCTION: snpgdsAlleleSwitch
Strand-switching at 50 SNP locus/loci.
Unable to determine switching at 10 SNP locus/loci.
FUNCTION: snpgdsApartSelection
Fri Dec 20 06:12:57 2024 Chromosome 1, # of SNPs: 367
Fri Dec 20 06:12:57 2024 Chromosome 2, # of SNPs: 367
Fri Dec 20 06:12:57 2024 Chromosome 3, # of SNPs: 317
Fri Dec 20 06:12:57 2024 Chromosome 4, # of SNPs: 295
Fri Dec 20 06:12:57 2024 Chromosome 5, # of SNPs: 295
Fri Dec 20 06:12:57 2024 Chromosome 6, # of SNPs: 283
Fri Dec 20 06:12:57 2024 Chromosome 7, # of SNPs: 245
Fri Dec 20 06:12:57 2024 Chromosome 8, # of SNPs: 234
Fri Dec 20 06:12:57 2024 Chromosome 9, # of SNPs: 202
Fri Dec 20 06:12:57 2024 Chromosome 10, # of SNPs: 224
Fri Dec 20 06:12:57 2024 Chromosome 11, # of SNPs: 223
Fri Dec 20 06:12:57 2024 Chromosome 12, # of SNPs: 208
Fri Dec 20 06:12:57 2024 Chromosome 13, # of SNPs: 172
Fri Dec 20 06:12:57 2024 Chromosome 14, # of SNPs: 147
Fri Dec 20 06:12:57 2024 Chromosome 15, # of SNPs: 121
Fri Dec 20 06:12:57 2024 Chromosome 16, # of SNPs: 129
Fri Dec 20 06:12:57 2024 Chromosome 17, # of SNPs: 116
Fri Dec 20 06:12:57 2024 Chromosome 18, # of SNPs: 129
Fri Dec 20 06:12:57 2024 Chromosome 19, # of SNPs: 73
Fri Dec 20 06:12:57 2024 Chromosome 20, # of SNPs: 106
Fri Dec 20 06:12:57 2024 Chromosome 21, # of SNPs: 62
Fri Dec 20 06:12:57 2024 Chromosome 22, # of SNPs: 51
Fri Dec 20 06:12:57 2024 Chromosome 23, # of SNPs: 204
Total # of SNPs selected:4570
FUNCTION: snpgdsBED2GDS
Start file conversion from PLINK BED to SNP GDS ...
BED file: "F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/plinkhapmap.bed.gz"
SNP-major mode (Sample X SNP), 45.7K
FAM file: "F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/plinkhapmap.fam.gz"
BIM file: "F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/plinkhapmap.bim.gz"
Fri Dec 20 06:12:57 2024 (store sample id, snp id, position, and chromosome)
start writing: 60 samples, 5000 SNPs ...
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:12:57 2024 Done.
Optimize the access efficiency ...
Clean up the fragments of GDS file:
open the file 'HapMap.gds' (98.1K)
# of fragments: 38
save to 'HapMap.gds.tmp'
rename 'HapMap.gds.tmp' (97.8K, reduced: 240B)
# of fragments: 18
FUNCTION: snpgdsClose
FUNCTION: snpgdsCombineGeno
Create a GDS genotype file:
The new dataset consists of 10 samples and 3000 SNPs
write sample.id
write snp.id
write snp.rs.id
write snp.position
write snp.chromosome
write snp.allele
SNP genotypes are stored in SNP-major mode (Sample X SNP).
Create a GDS genotype file:
The new dataset consists of 20 samples and 3000 SNPs
write sample.id
write snp.id
write snp.rs.id
write snp.position
write snp.chromosome
write snp.allele
SNP genotypes are stored in SNP-major mode (Sample X SNP).
Merge SNP GDS files:
open 't1.gds' ...
10 samples, 3000 SNPs
open 't2.gds' ...
20 samples, 3000 SNPs
Concatenating samples (mapping to the first GDS file) ...
reference: 3000 SNPs (100.0%)
file 2: 0 allele flips, 0 ambiguous locus/loci
[no flip]: 3000
create 'test.gds': 30 samples, 3000 SNPs
FileFormat = SNP_ARRAY
writing genotypes ...
Clean up the fragments of GDS file:
open the file 'test.gds' (46.2K)
# of fragments: 32
save to 'test.gds.tmp'
rename 'test.gds.tmp' (46.0K, reduced: 204B)
# of fragments: 15
Done.
Create a GDS genotype file:
The new dataset consists of 279 samples and 100 SNPs
write sample.id
write snp.id
write snp.rs.id
write snp.position
write snp.chromosome
write snp.allele
SNP genotypes are stored in SNP-major mode (Sample X SNP).
Create a GDS genotype file:
The new dataset consists of 279 samples and 200 SNPs
write sample.id
write snp.id
write snp.rs.id
write snp.position
write snp.chromosome
write snp.allele
SNP genotypes are stored in SNP-major mode (Sample X SNP).
Merge SNP GDS files:
open 't1.gds' ...
279 samples, 100 SNPs
open 't2.gds' ...
279 samples, 200 SNPs
Concatenating SNPs ...
create 'test.gds': 279 samples, 300 SNPs
FileFormat = SNP_ARRAY
writing genotypes ...
Clean up the fragments of GDS file:
open the file 'test.gds' (19.1K)
# of fragments: 32
save to 'test.gds.tmp'
rename 'test.gds.tmp' (18.9K, reduced: 204B)
# of fragments: 15
Done.
FUNCTION: snpgdsCreateGeno
Principal Component Analysis (PCA) on genotypes:
Excluding 42 SNPs on non-autosomes
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 958
using 1 thread
# of principal components: 32
PCA: the sum of all selected genotypes (0,1,2) = 264760
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:12:58 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:12:58 2024 Begin (eigenvalues and eigenvectors)
Fri Dec 20 06:12:58 2024 Done.
FUNCTION: snpgdsCreateGenoSet
SNP pruning based on LD:
Excluding 365 SNPs on non-autosomes
Excluding 139 SNPs (monomorphic: TRUE, MAF: 0.005, missing rate: 0.05)
# of samples: 279
# of SNPs: 8,584
using 1 thread
sliding window: 500,000 basepairs, Inf SNPs
|LD| threshold: 0.2
method: composite
Chrom 1: |====================|====================|
74.30%, 532 / 716 (Fri Dec 20 06:12:59 2024)
Chrom 2: |====================|====================|
72.24%, 536 / 742 (Fri Dec 20 06:12:59 2024)
Chrom 3: |====================|====================|
73.40%, 447 / 609 (Fri Dec 20 06:12:59 2024)
Chrom 4: |====================|====================|
72.42%, 407 / 562 (Fri Dec 20 06:12:59 2024)
Chrom 5: |====================|====================|
75.80%, 429 / 566 (Fri Dec 20 06:12:59 2024)
Chrom 6: |====================|====================|
73.81%, 417 / 565 (Fri Dec 20 06:12:59 2024)
Chrom 7: |====================|====================|
75.21%, 355 / 472 (Fri Dec 20 06:12:59 2024)
Chrom 8: |====================|====================|
69.67%, 340 / 488 (Fri Dec 20 06:12:59 2024)
Chrom 9: |====================|====================|
76.92%, 320 / 416 (Fri Dec 20 06:12:59 2024)
Chrom 10: |====================|====================|
73.08%, 353 / 483 (Fri Dec 20 06:12:59 2024)
Chrom 11: |====================|====================|
76.51%, 342 / 447 (Fri Dec 20 06:12:59 2024)
Chrom 12: |====================|====================|
74.71%, 319 / 427 (Fri Dec 20 06:12:59 2024)
Chrom 13: |====================|====================|
76.74%, 264 / 344 (Fri Dec 20 06:12:59 2024)
Chrom 14: |====================|====================|
76.24%, 215 / 282 (Fri Dec 20 06:12:59 2024)
Chrom 15: |====================|====================|
75.95%, 199 / 262 (Fri Dec 20 06:12:59 2024)
Chrom 16: |====================|====================|
70.86%, 197 / 278 (Fri Dec 20 06:12:59 2024)
Chrom 17: |====================|====================|
76.33%, 158 / 207 (Fri Dec 20 06:12:59 2024)
Chrom 18: |====================|====================|
73.31%, 195 / 266 (Fri Dec 20 06:12:59 2024)
Chrom 19: |====================|====================|
82.50%, 99 / 120 (Fri Dec 20 06:12:59 2024)
Chrom 20: |====================|====================|
70.31%, 161 / 229 (Fri Dec 20 06:12:59 2024)
Chrom 21: |====================|====================|
75.40%, 95 / 126 (Fri Dec 20 06:12:59 2024)
Chrom 22: |====================|====================|
75.86%, 88 / 116 (Fri Dec 20 06:12:59 2024)
6,468 markers are selected in total.
Create a GDS genotype file:
The new dataset consists of 279 samples and 6468 SNPs
write sample.id
write snp.id
write snp.rs.id
write snp.position
write snp.chromosome
write snp.allele
SNP genotypes are stored in SNP-major mode (Sample X SNP).
FUNCTION: snpgdsCutTree
Individual dissimilarity analysis on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
Dissimilarity: the sum of all selected genotypes (0,1,2) = 2446510
Dissimilarity: Fri Dec 20 06:12:59 2024 0%
Dissimilarity: Fri Dec 20 06:13:00 2024 100%
Determine groups by permutation (Z threshold: 15, outlier threshold: 5):
Create 3 groups.
Create 4 groups.
FUNCTION: snpgdsDiss
Individual dissimilarity analysis on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
Dissimilarity: the sum of all selected genotypes (0,1,2) = 2446510
Dissimilarity: Fri Dec 20 06:13:01 2024 0%
Dissimilarity: Fri Dec 20 06:13:02 2024 100%
Determine groups by permutation (Z threshold: 15, outlier threshold: 5):
Create 3 groups.
FUNCTION: snpgdsDrawTree
Individual dissimilarity analysis on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
Dissimilarity: the sum of all selected genotypes (0,1,2) = 2446510
Dissimilarity: Fri Dec 20 06:13:03 2024 0%
Dissimilarity: Fri Dec 20 06:13:04 2024 100%
Determine groups by permutation (Z threshold: 15, outlier threshold: 5):
Create 3 groups.
FUNCTION: snpgdsEIGMIX
Eigen-analysis on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
Eigen-analysis: the sum of all selected genotypes (0,1,2) = 2446510
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:04 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:13:05 2024 Begin (eigenvalues and eigenvectors)
Fri Dec 20 06:13:05 2024 Done.
FUNCTION: snpgdsErrMsg
FUNCTION: snpgdsExampleFileName
FUNCTION: snpgdsFst
Fst estimation on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
Method: Weir & Cockerham, 1984
# of Populations: 4
CEU (92), HCB (47), JPT (47), YRI (93)
Fst estimation on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
Method: Weir & Hill, 2002
# of Populations: 4
CEU (92), HCB (47), JPT (47), YRI (93)
FUNCTION: snpgdsGDS2BED
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: 0.95)
Converting from GDS to PLINK binary PED:
Working space: 279 samples, 8722 SNPs
Output a BIM file.
Output a BED file ...
Fri Dec 20 06:13:05 2024 0%
Fri Dec 20 06:13:05 2024 100%
Done.
FUNCTION: snpgdsGDS2Eigen
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: 0.95)
Converting from GDS to EIGENSOFT:
save to *.snp: 8722 snps
save to *.ind: 279 samples
Output: Fri Dec 20 06:13:06 2024 0%
Output: Fri Dec 20 06:13:06 2024 100%
Done.
FUNCTION: snpgdsGDS2PED
Converting from GDS to PLINK PED:
Output a MAP file DONE.
Output a PED file ...
Output: Fri Dec 20 06:13:06 2024 0%
Output: Fri Dec 20 06:13:06 2024 100%
FUNCTION: snpgdsGEN2GDS
running snpgdsGEN2GDS ...
FUNCTION: snpgdsGRM
Genetic Relationship Matrix (GRM, GCTA):
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 2446510
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:06 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:13:07 2024 Done.
Genetic Relationship Matrix (GRM, GCTA):
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 2446510
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:07 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Saving to the GDS file:
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:08 2024 Done.
FUNCTION: snpgdsGetGeno
Genotype matrix: 1000 SNPs X 279 samples
Genotype matrix: 279 samples X 1000 SNPs
FUNCTION: snpgdsHCluster
Individual dissimilarity analysis on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
Dissimilarity: the sum of all selected genotypes (0,1,2) = 2446510
Dissimilarity: Fri Dec 20 06:13:08 2024 0%
Dissimilarity: Fri Dec 20 06:13:09 2024 100%
Determine groups by permutation (Z threshold: 15, outlier threshold: 5):
Create 3 groups.
FUNCTION: snpgdsHWE
Keeping 716 SNPs according to chromosome 1
Excluding 160 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
FUNCTION: snpgdsIBDKING
IBD analysis (KING method of moment) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1,217 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 92
# of SNPs: 7,506
using 1 thread
No family is specified, and all individuals are treated as singletons.
Relationship inference in the presence of population stratification.
KING IBD: the sum of all selected genotypes (0,1,2) = 702139
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:11 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:11 2024 Done.
IBD analysis (KING method of moment) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1,217 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 92
# of SNPs: 7,506
using 1 thread
No family is specified, and all individuals are treated as singletons.
Relationship inference in the presence of population stratification.
KING IBD: the sum of all selected genotypes (0,1,2) = 702139
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:11 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:11 2024 Done.
IBD analysis (KING method of moment) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1,217 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 92
# of SNPs: 7,506
using 1 thread
# of families: 20, and within- and between-family relationship are estimated differently.
Relationship inference in the presence of population stratification.
KING IBD: the sum of all selected genotypes (0,1,2) = 702139
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:12 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:12 2024 Done.
IBD analysis (KING method of moment) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1,217 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 92
# of SNPs: 7,506
using 1 thread
Relationship inference in a homogeneous population.
KING IBD: the sum of all selected genotypes (0,1,2) = 702139
Fri Dec 20 06:13:12 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:12 2024 Done.
IBD analysis (KING method of moment) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1,217 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 92
# of SNPs: 7,506
using 1 thread
Relationship inference in a homogeneous population.
KING IBD: the sum of all selected genotypes (0,1,2) = 702139
Fri Dec 20 06:13:12 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:13:13 2024 Done.
FUNCTION: snpgdsIBDMLE
SNP pruning based on LD:
Excluding 365 SNPs on non-autosomes
Excluding 1,581 SNPs (monomorphic: TRUE, MAF: 0.05, missing rate: 0.05)
# of samples: 30
# of SNPs: 7,142
using 1 thread
sliding window: 500,000 basepairs, Inf SNPs
|LD| threshold: 0.2
method: composite
Chrom 1: |====================|====================|
54.75%, 392 / 716 (Fri Dec 20 06:13:13 2024)
Chrom 2: |====================|====================|
54.85%, 407 / 742 (Fri Dec 20 06:13:13 2024)
Chrom 3: |====================|====================|
55.99%, 341 / 609 (Fri Dec 20 06:13:13 2024)
Chrom 4: |====================|====================|
56.58%, 318 / 562 (Fri Dec 20 06:13:13 2024)
Chrom 5: |====================|====================|
56.36%, 319 / 566 (Fri Dec 20 06:13:13 2024)
Chrom 6: |====================|====================|
53.45%, 302 / 565 (Fri Dec 20 06:13:13 2024)
Chrom 7: |====================|====================|
55.72%, 263 / 472 (Fri Dec 20 06:13:13 2024)
Chrom 8: |====================|====================|
50.82%, 248 / 488 (Fri Dec 20 06:13:13 2024)
Chrom 9: |====================|====================|
54.81%, 228 / 416 (Fri Dec 20 06:13:13 2024)
Chrom 10: |====================|====================|
49.90%, 241 / 483 (Fri Dec 20 06:13:13 2024)
Chrom 11: |====================|====================|
54.81%, 245 / 447 (Fri Dec 20 06:13:13 2024)
Chrom 12: |====================|====================|
54.57%, 233 / 427 (Fri Dec 20 06:13:13 2024)
Chrom 13: |====================|====================|
53.49%, 184 / 344 (Fri Dec 20 06:13:13 2024)
Chrom 14: |====================|====================|
56.03%, 158 / 282 (Fri Dec 20 06:13:13 2024)
Chrom 15: |====================|====================|
54.58%, 143 / 262 (Fri Dec 20 06:13:13 2024)
Chrom 16: |====================|====================|
54.68%, 152 / 278 (Fri Dec 20 06:13:13 2024)
Chrom 17: |====================|====================|
55.56%, 115 / 207 (Fri Dec 20 06:13:13 2024)
Chrom 18: |====================|====================|
55.64%, 148 / 266 (Fri Dec 20 06:13:13 2024)
Chrom 19: |====================|====================|
66.67%, 80 / 120 (Fri Dec 20 06:13:13 2024)
Chrom 20: |====================|====================|
53.28%, 122 / 229 (Fri Dec 20 06:13:13 2024)
Chrom 21: |====================|====================|
50.79%, 64 / 126 (Fri Dec 20 06:13:13 2024)
Chrom 22: |====================|====================|
51.72%, 60 / 116 (Fri Dec 20 06:13:13 2024)
4,763 markers are selected in total.
Identity-By-Descent analysis (MLE) on genotypes:
Excluding 8,838 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 30
# of SNPs: 250
using 1 thread
MLE IBD: the sum of all selected genotypes (0,1,2) = 8025
MLE IBD: Fri Dec 20 06:13:13 2024 0%
MLE IBD: Fri Dec 20 06:13:14 2024 100%
Identity-By-Descent analysis (MLE) on genotypes:
Excluding 8,838 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 25
# of SNPs: 250
using 1 thread
Specifying allele frequencies, mean: 0.536, sd: 0.286
MLE IBD: the sum of all selected genotypes (0,1,2) = 6690
MLE IBD: Fri Dec 20 06:13:14 2024 0%
MLE IBD: Fri Dec 20 06:13:14 2024 100%
FUNCTION: snpgdsIBDMLELogLik
SNP pruning based on LD:
Excluding 365 SNPs on non-autosomes
Excluding 1,581 SNPs (monomorphic: TRUE, MAF: 0.05, missing rate: 0.05)
# of samples: 30
# of SNPs: 7,142
using 1 thread
sliding window: 500,000 basepairs, Inf SNPs
|LD| threshold: 0.2
method: composite
Chrom 1: |====================|====================|
54.75%, 392 / 716 (Fri Dec 20 06:13:14 2024)
Chrom 2: |====================|====================|
54.85%, 407 / 742 (Fri Dec 20 06:13:14 2024)
Chrom 3: |====================|====================|
55.99%, 341 / 609 (Fri Dec 20 06:13:14 2024)
Chrom 4: |====================|====================|
56.58%, 318 / 562 (Fri Dec 20 06:13:14 2024)
Chrom 5: |====================|====================|
56.36%, 319 / 566 (Fri Dec 20 06:13:14 2024)
Chrom 6: |====================|====================|
53.45%, 302 / 565 (Fri Dec 20 06:13:14 2024)
Chrom 7: |====================|====================|
55.72%, 263 / 472 (Fri Dec 20 06:13:14 2024)
Chrom 8: |====================|====================|
50.82%, 248 / 488 (Fri Dec 20 06:13:14 2024)
Chrom 9: |====================|====================|
54.81%, 228 / 416 (Fri Dec 20 06:13:14 2024)
Chrom 10: |====================|====================|
49.90%, 241 / 483 (Fri Dec 20 06:13:14 2024)
Chrom 11: |====================|====================|
54.81%, 245 / 447 (Fri Dec 20 06:13:14 2024)
Chrom 12: |====================|====================|
54.57%, 233 / 427 (Fri Dec 20 06:13:14 2024)
Chrom 13: |====================|====================|
53.49%, 184 / 344 (Fri Dec 20 06:13:14 2024)
Chrom 14: |====================|====================|
56.03%, 158 / 282 (Fri Dec 20 06:13:14 2024)
Chrom 15: |====================|====================|
54.58%, 143 / 262 (Fri Dec 20 06:13:14 2024)
Chrom 16: |====================|====================|
54.68%, 152 / 278 (Fri Dec 20 06:13:14 2024)
Chrom 17: |====================|====================|
55.56%, 115 / 207 (Fri Dec 20 06:13:14 2024)
Chrom 18: |====================|====================|
55.64%, 148 / 266 (Fri Dec 20 06:13:14 2024)
Chrom 19: |====================|====================|
66.67%, 80 / 120 (Fri Dec 20 06:13:14 2024)
Chrom 20: |====================|====================|
53.28%, 122 / 229 (Fri Dec 20 06:13:14 2024)
Chrom 21: |====================|====================|
50.79%, 64 / 126 (Fri Dec 20 06:13:14 2024)
Chrom 22: |====================|====================|
51.72%, 60 / 116 (Fri Dec 20 06:13:14 2024)
4,763 markers are selected in total.
Identity-By-Descent analysis (MLE) on genotypes:
Excluding 8,838 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 30
# of SNPs: 250
using 1 thread
MLE IBD: the sum of all selected genotypes (0,1,2) = 8025
MLE IBD: Fri Dec 20 06:13:14 2024 0%
MLE IBD: Fri Dec 20 06:13:15 2024 100%
Identity-By-Descent analysis (MLE) on genotypes:
Excluding 8,838 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 25
# of SNPs: 250
using 1 thread
Specifying allele frequencies, mean: 0.536, sd: 0.286
MLE IBD: the sum of all selected genotypes (0,1,2) = 6690
MLE IBD: Fri Dec 20 06:13:15 2024 0%
MLE IBD: Fri Dec 20 06:13:15 2024 100%
FUNCTION: snpgdsIBDMoM
IBD analysis (PLINK method of moment) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1,217 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 92
# of SNPs: 7,506
using 1 thread
PLINK IBD: the sum of all selected genotypes (0,1,2) = 702139
Fri Dec 20 06:13:15 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:15 2024 Done.
IBD analysis (PLINK method of moment) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 563 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 93
# of SNPs: 8,160
using 1 thread
PLINK IBD: the sum of all selected genotypes (0,1,2) = 755648
Fri Dec 20 06:13:15 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:15 2024 Done.
IBD analysis (PLINK method of moment) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 563 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 93
# of SNPs: 8,160
using 1 thread
Specifying allele frequencies, mean: 0.500, sd: 0.315
*** A correction factor based on allele count is not used, since the allele frequencies are specified.
PLINK IBD: the sum of all selected genotypes (0,1,2) = 755648
Fri Dec 20 06:13:15 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:15 2024 Done.
IBD analysis (PLINK method of moment) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 563 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 25
# of SNPs: 8,160
using 1 thread
Specifying allele frequencies, mean: 0.500, sd: 0.315
*** A correction factor based on allele count is not used, since the allele frequencies are specified.
PLINK IBD: the sum of all selected genotypes (0,1,2) = 203285
Fri Dec 20 06:13:15 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:15 2024 Done.
FUNCTION: snpgdsIBDSelection
IBD analysis (PLINK method of moment) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 563 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 93
# of SNPs: 8,160
using 1 thread
PLINK IBD: the sum of all selected genotypes (0,1,2) = 755648
Fri Dec 20 06:13:16 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:16 2024 Done.
FUNCTION: snpgdsIBS
Identity-By-State (IBS) analysis on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
IBS: the sum of all selected genotypes (0,1,2) = 2446510
Fri Dec 20 06:13:16 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:16 2024 Done.
FUNCTION: snpgdsIBSNum
Identity-By-State (IBS) analysis on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
IBS: the sum of all selected genotypes (0,1,2) = 2446510
Fri Dec 20 06:13:16 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:16 2024 Done.
FUNCTION: snpgdsIndInb
Estimating individual inbreeding coefficients:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
FUNCTION: snpgdsIndInbCoef
FUNCTION: snpgdsIndivBeta
Individual Inbreeding and Relatedness (beta estimator):
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
Individual Beta: the sum of all selected genotypes (0,1,2) = 2446510
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:17 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:17 2024 Done.
FUNCTION: snpgdsLDMat
Linkage Disequilibrium (LD) estimation on genotypes:
# of samples: 279
# of SNPs: 203
using 1 thread
method: composite
LD matrix: the sum of all selected genotypes (0,1,2) = 56582
Linkage Disequilibrium (LD) estimation on genotypes:
# of samples: 279
# of SNPs: 203
using 1 thread
sliding window size: 203
method: composite
LD matrix: the sum of all selected genotypes (0,1,2) = 56582
FUNCTION: snpgdsLDpair
FUNCTION: snpgdsLDpruning
SNP pruning based on LD:
Excluding 365 SNPs on non-autosomes
Excluding 139 SNPs (monomorphic: TRUE, MAF: 0.005, missing rate: 0.05)
# of samples: 279
# of SNPs: 8,584
using 1 thread
sliding window: 500,000 basepairs, Inf SNPs
|LD| threshold: 0.2
method: composite
Chrom 1: |====================|====================|
74.30%, 532 / 716 (Fri Dec 20 06:13:17 2024)
Chrom 2: |====================|====================|
72.24%, 536 / 742 (Fri Dec 20 06:13:17 2024)
Chrom 3: |====================|====================|
73.40%, 447 / 609 (Fri Dec 20 06:13:17 2024)
Chrom 4: |====================|====================|
72.42%, 407 / 562 (Fri Dec 20 06:13:17 2024)
Chrom 5: |====================|====================|
75.80%, 429 / 566 (Fri Dec 20 06:13:17 2024)
Chrom 6: |====================|====================|
73.81%, 417 / 565 (Fri Dec 20 06:13:17 2024)
Chrom 7: |====================|====================|
75.21%, 355 / 472 (Fri Dec 20 06:13:17 2024)
Chrom 8: |====================|====================|
69.67%, 340 / 488 (Fri Dec 20 06:13:18 2024)
Chrom 9: |====================|====================|
76.92%, 320 / 416 (Fri Dec 20 06:13:18 2024)
Chrom 10: |====================|====================|
73.08%, 353 / 483 (Fri Dec 20 06:13:18 2024)
Chrom 11: |====================|====================|
76.51%, 342 / 447 (Fri Dec 20 06:13:18 2024)
Chrom 12: |====================|====================|
74.71%, 319 / 427 (Fri Dec 20 06:13:18 2024)
Chrom 13: |====================|====================|
76.74%, 264 / 344 (Fri Dec 20 06:13:18 2024)
Chrom 14: |====================|====================|
76.24%, 215 / 282 (Fri Dec 20 06:13:18 2024)
Chrom 15: |====================|====================|
75.95%, 199 / 262 (Fri Dec 20 06:13:18 2024)
Chrom 16: |====================|====================|
70.86%, 197 / 278 (Fri Dec 20 06:13:18 2024)
Chrom 17: |====================|====================|
76.33%, 158 / 207 (Fri Dec 20 06:13:18 2024)
Chrom 18: |====================|====================|
73.31%, 195 / 266 (Fri Dec 20 06:13:18 2024)
Chrom 19: |====================|====================|
82.50%, 99 / 120 (Fri Dec 20 06:13:18 2024)
Chrom 20: |====================|====================|
70.31%, 161 / 229 (Fri Dec 20 06:13:18 2024)
Chrom 21: |====================|====================|
75.40%, 95 / 126 (Fri Dec 20 06:13:18 2024)
Chrom 22: |====================|====================|
75.86%, 88 / 116 (Fri Dec 20 06:13:18 2024)
6,468 markers are selected in total.
List of 22
$ chr1 : int [1:532] 1 2 4 5 7 10 12 14 15 16 ...
$ chr2 : int [1:536] 717 718 719 720 721 723 724 725 726 727 ...
$ chr3 : int [1:447] 1459 1461 1464 1466 1468 1469 1471 1472 1473 1476 ...
$ chr4 : int [1:407] 2068 2069 2070 2071 2072 2074 2075 2076 2077 2078 ...
$ chr5 : int [1:429] 2630 2631 2635 2636 2637 2638 2640 2642 2643 2645 ...
$ chr6 : int [1:417] 3196 3197 3198 3200 3201 3204 3205 3206 3207 3208 ...
$ chr7 : int [1:355] 3761 3762 3763 3766 3767 3768 3770 3771 3772 3773 ...
$ chr8 : int [1:340] 4233 4234 4235 4236 4237 4238 4239 4240 4241 4242 ...
$ chr9 : int [1:320] 4721 4722 4724 4727 4728 4730 4731 4732 4733 4735 ...
$ chr10: int [1:353] 5138 5139 5140 5143 5144 5145 5146 5147 5148 5149 ...
$ chr11: int [1:342] 5620 5623 5624 5625 5626 5628 5629 5630 5631 5632 ...
$ chr12: int [1:319] 6067 6068 6069 6070 6073 6074 6075 6077 6078 6079 ...
$ chr13: int [1:264] 6494 6497 6498 6499 6500 6501 6503 6505 6507 6509 ...
$ chr14: int [1:215] 6840 6841 6842 6843 6844 6845 6846 6847 6848 6850 ...
$ chr15: int [1:199] 7120 7121 7122 7124 7125 7126 7127 7128 7129 7130 ...
$ chr16: int [1:197] 7382 7383 7384 7385 7387 7388 7389 7391 7392 7394 ...
$ chr17: int [1:158] 7660 7661 7662 7663 7664 7665 7666 7667 7668 7669 ...
$ chr18: int [1:195] 7867 7868 7869 7870 7871 7872 7873 7874 7875 7877 ...
$ chr19: int [1:99] 8133 8135 8136 8137 8138 8139 8140 8141 8142 8144 ...
$ chr20: int [1:161] 8253 8254 8257 8258 8259 8260 8261 8262 8265 8266 ...
$ chr21: int [1:95] 8482 8484 8485 8486 8487 8488 8489 8490 8491 8492 ...
$ chr22: int [1:88] 8608 8609 8610 8612 8613 8614 8615 8617 8618 8620 ...
FUNCTION: snpgdsMergeGRM
Genetic Relationship Matrix (GRM, GCTA):
Excluding 2,288 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 6,800
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 1908966
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:18 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:18 2024 Done.
Genetic Relationship Matrix (GRM, GCTA):
Excluding 5,688 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 3,400
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 951558
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:18 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Saving to the GDS file:
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:19 2024 Done.
Genetic Relationship Matrix (GRM, GCTA):
Excluding 5,688 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 3,400
using 1 thread
GRM Calculation: the sum of all selected genotypes (0,1,2) = 957408
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:19 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Saving to the GDS file:
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:20 2024 Done.
GRM merging:
open 'tmp1.gds' (3,400 variants)
open 'tmp2.gds' (3,400 variants)
Weight: 0.5, 0.5
Output: tmp.gds
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
GRM merging:
open 'tmp1.gds' (3,400 variants)
open 'tmp2.gds' (3,400 variants)
Weight: 0.5, 0.5
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
FUNCTION: snpgdsOpen
FUNCTION: snpgdsOption
FUNCTION: snpgdsPCA
Principal Component Analysis (PCA) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
# of principal components: 32
PCA: the sum of all selected genotypes (0,1,2) = 2446510
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:21 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:13:22 2024 Begin (eigenvalues and eigenvectors)
Fri Dec 20 06:13:22 2024 Done.
FUNCTION: snpgdsPCACorr
Principal Component Analysis (PCA) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
# of principal components: 32
PCA: the sum of all selected genotypes (0,1,2) = 2446510
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:22 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:13:23 2024 Begin (eigenvalues and eigenvectors)
Fri Dec 20 06:13:23 2024 Done.
SNP Correlation:
# of samples: 279
# of SNPs: 9,088
using 1 thread
Correlation: the sum of all selected genotypes (0,1,2) = 2553065
Fri Dec 20 06:13:23 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:23 2024 Done.
SNP Correlation:
# of samples: 279
# of SNPs: 9,088
using 1 thread
Creating 'test.gds' ...
Correlation: the sum of all selected genotypes (0,1,2) = 2553065
Fri Dec 20 06:13:23 2024
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:23 2024 Done.
FUNCTION: snpgdsPCASNPLoading
Principal Component Analysis (PCA) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
# of principal components: 8
PCA: the sum of all selected genotypes (0,1,2) = 2446510
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:23 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:13:24 2024 Begin (eigenvalues and eigenvectors)
Fri Dec 20 06:13:24 2024 Done.
SNP Loading:
# of samples: 279
# of SNPs: 8,722
using 1 thread
using the top 8 eigenvectors
SNP Loading: the sum of all selected genotypes (0,1,2) = 2446510
Fri Dec 20 06:13:24 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:24 2024 Done.
FUNCTION: snpgdsPCASampLoading
Principal Component Analysis (PCA) on genotypes:
Excluding 365 SNPs on non-autosomes
Excluding 1 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 8,722
using 1 thread
# of principal components: 8
PCA: the sum of all selected genotypes (0,1,2) = 2446510
CPU capabilities: Double-Precision SSE2
Fri Dec 20 06:13:24 2024 (internal increment: 16308)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 1s
Fri Dec 20 06:13:25 2024 Begin (eigenvalues and eigenvectors)
Fri Dec 20 06:13:25 2024 Done.
SNP Loading:
# of samples: 279
# of SNPs: 8,722
using 1 thread
using the top 8 eigenvectors
SNP Loading: the sum of all selected genotypes (0,1,2) = 2446510
Fri Dec 20 06:13:25 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:25 2024 Done.
Sample Loading:
# of samples: 100
# of SNPs: 8,722
using 1 thread
using the top 8 eigenvectors
Sample Loading: the sum of all selected genotypes (0,1,2) = 878146
Fri Dec 20 06:13:25 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:25 2024 Done.
FUNCTION: snpgdsPED2GDS
Converting from GDS to PLINK PED:
Output a MAP file DONE.
Output a PED file ...
Output: Fri Dec 20 06:13:25 2024 0%
Output: Fri Dec 20 06:13:26 2024 100%
PLINK PED/MAP to GDS Format:
Import 9088 variants from 'tmp.map'
Chromosome:
1 10 11 12 13 14 15 16 17 18 19 2 20 21 22 3 4 5 6 7
716 483 447 427 344 282 262 278 207 266 120 742 229 126 116 609 562 566 565 472
8 9 X
488 416 365
Reading 'tmp.ped'
Output: 'test.gds'
Import 279 samples
Transpose the genotypic matrix ...
Done.
Optimize the access efficiency ...
Clean up the fragments of GDS file:
open the file 'test.gds' (1.3M)
# of fragments: 50
save to 'test.gds.tmp'
rename 'test.gds.tmp' (711.4K, reduced: 618.7K)
# of fragments: 26
FUNCTION: snpgdsPairIBD
SNP pruning based on LD:
Excluding 365 SNPs on non-autosomes
Excluding 1,646 SNPs (monomorphic: TRUE, MAF: 0.05, missing rate: 0.05)
# of samples: 93
# of SNPs: 7,077
using 1 thread
sliding window: 500,000 basepairs, Inf SNPs
|LD| threshold: 0.2
method: composite
Chrom 1: |====================|====================|
62.29%, 446 / 716 (Fri Dec 20 06:13:27 2024)
Chrom 2: |====================|====================|
62.26%, 462 / 742 (Fri Dec 20 06:13:27 2024)
Chrom 3: |====================|====================|
60.10%, 366 / 609 (Fri Dec 20 06:13:27 2024)
Chrom 4: |====================|====================|
64.41%, 362 / 562 (Fri Dec 20 06:13:27 2024)
Chrom 5: |====================|====================|
62.90%, 356 / 566 (Fri Dec 20 06:13:27 2024)
Chrom 6: |====================|====================|
60.18%, 340 / 565 (Fri Dec 20 06:13:27 2024)
Chrom 7: |====================|====================|
63.14%, 298 / 472 (Fri Dec 20 06:13:27 2024)
Chrom 8: |====================|====================|
57.58%, 281 / 488 (Fri Dec 20 06:13:27 2024)
Chrom 9: |====================|====================|
62.98%, 262 / 416 (Fri Dec 20 06:13:27 2024)
Chrom 10: |====================|====================|
60.46%, 292 / 483 (Fri Dec 20 06:13:27 2024)
Chrom 11: |====================|====================|
63.09%, 282 / 447 (Fri Dec 20 06:13:27 2024)
Chrom 12: |====================|====================|
62.76%, 268 / 427 (Fri Dec 20 06:13:27 2024)
Chrom 13: |====================|====================|
63.08%, 217 / 344 (Fri Dec 20 06:13:27 2024)
Chrom 14: |====================|====================|
63.83%, 180 / 282 (Fri Dec 20 06:13:27 2024)
Chrom 15: |====================|====================|
63.74%, 167 / 262 (Fri Dec 20 06:13:27 2024)
Chrom 16: |====================|====================|
62.23%, 173 / 278 (Fri Dec 20 06:13:27 2024)
Chrom 17: |====================|====================|
65.70%, 136 / 207 (Fri Dec 20 06:13:27 2024)
Chrom 18: |====================|====================|
59.40%, 158 / 266 (Fri Dec 20 06:13:27 2024)
Chrom 19: |====================|====================|
68.33%, 82 / 120 (Fri Dec 20 06:13:27 2024)
Chrom 20: |====================|====================|
66.38%, 152 / 229 (Fri Dec 20 06:13:27 2024)
Chrom 21: |====================|====================|
61.11%, 77 / 126 (Fri Dec 20 06:13:27 2024)
Chrom 22: |====================|====================|
57.76%, 67 / 116 (Fri Dec 20 06:13:27 2024)
5,424 markers are selected in total.
Identity-By-Descent analysis (MLE) on genotypes:
Excluding 8,838 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 25
# of SNPs: 250
using 1 thread
Specifying allele frequencies, mean: 0.508, sd: 0.281
MLE IBD: the sum of all selected genotypes (0,1,2) = 6317
MLE IBD: Fri Dec 20 06:13:27 2024 0%
MLE IBD: Fri Dec 20 06:13:27 2024 100%
IBD analysis (PLINK method of moment) on genotypes:
Excluding 8,838 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 25
# of SNPs: 250
using 1 thread
Specifying allele frequencies, mean: 0.508, sd: 0.281
*** A correction factor based on allele count is not used, since the allele frequencies are specified.
PLINK IBD: the sum of all selected genotypes (0,1,2) = 6317
Fri Dec 20 06:13:27 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:27 2024 Done.
Identity-By-Descent analysis (MLE) on genotypes:
Excluding 8,838 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 25
# of SNPs: 250
using 1 thread
Specifying allele frequencies, mean: 0.508, sd: 0.281
MLE IBD: the sum of all selected genotypes (0,1,2) = 6317
MLE IBD: Fri Dec 20 06:13:27 2024 0%
MLE IBD: Fri Dec 20 06:13:28 2024 100%
Genotype matrix: 250 SNPs X 25 samples
[1] -384.5064
[1] -379.8635
[1] -389.2882
[1] -390.0637
[1] -405.3267
[1] -386.6771
[1] -382.3052
[1] -375.7884
[1] -400.5859
[1] -379.9675
[1] -372.4947
[1] -372.3346
[1] -393.543
[1] -387.7755
[1] -373.858
[1] -380.4349
[1] -389.0108
[1] -402.2013
[1] -393.1451
[1] -388.5999
[1] -383.8134
[1] -376.6837
[1] -385.4354
[1] -378.9947
FUNCTION: snpgdsPairIBDMLELogLik
SNP pruning based on LD:
Excluding 365 SNPs on non-autosomes
Excluding 1,646 SNPs (monomorphic: TRUE, MAF: 0.05, missing rate: 0.05)
# of samples: 93
# of SNPs: 7,077
using 1 thread
sliding window: 500,000 basepairs, Inf SNPs
|LD| threshold: 0.2
method: composite
Chrom 1: |====================|====================|
62.29%, 446 / 716 (Fri Dec 20 06:13:28 2024)
Chrom 2: |====================|====================|
62.26%, 462 / 742 (Fri Dec 20 06:13:28 2024)
Chrom 3: |====================|====================|
60.10%, 366 / 609 (Fri Dec 20 06:13:28 2024)
Chrom 4: |====================|====================|
64.41%, 362 / 562 (Fri Dec 20 06:13:28 2024)
Chrom 5: |====================|====================|
62.90%, 356 / 566 (Fri Dec 20 06:13:28 2024)
Chrom 6: |====================|====================|
60.18%, 340 / 565 (Fri Dec 20 06:13:28 2024)
Chrom 7: |====================|====================|
63.14%, 298 / 472 (Fri Dec 20 06:13:28 2024)
Chrom 8: |====================|====================|
57.58%, 281 / 488 (Fri Dec 20 06:13:28 2024)
Chrom 9: |====================|====================|
62.98%, 262 / 416 (Fri Dec 20 06:13:28 2024)
Chrom 10: |====================|====================|
60.46%, 292 / 483 (Fri Dec 20 06:13:28 2024)
Chrom 11: |====================|====================|
63.09%, 282 / 447 (Fri Dec 20 06:13:28 2024)
Chrom 12: |====================|====================|
62.76%, 268 / 427 (Fri Dec 20 06:13:28 2024)
Chrom 13: |====================|====================|
63.08%, 217 / 344 (Fri Dec 20 06:13:28 2024)
Chrom 14: |====================|====================|
63.83%, 180 / 282 (Fri Dec 20 06:13:28 2024)
Chrom 15: |====================|====================|
63.74%, 167 / 262 (Fri Dec 20 06:13:28 2024)
Chrom 16: |====================|====================|
62.23%, 173 / 278 (Fri Dec 20 06:13:28 2024)
Chrom 17: |====================|====================|
65.70%, 136 / 207 (Fri Dec 20 06:13:28 2024)
Chrom 18: |====================|====================|
59.40%, 158 / 266 (Fri Dec 20 06:13:28 2024)
Chrom 19: |====================|====================|
68.33%, 82 / 120 (Fri Dec 20 06:13:28 2024)
Chrom 20: |====================|====================|
66.38%, 152 / 229 (Fri Dec 20 06:13:28 2024)
Chrom 21: |====================|====================|
61.11%, 77 / 126 (Fri Dec 20 06:13:28 2024)
Chrom 22: |====================|====================|
57.76%, 67 / 116 (Fri Dec 20 06:13:28 2024)
5,424 markers are selected in total.
Identity-By-Descent analysis (MLE) on genotypes:
Excluding 8,838 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 25
# of SNPs: 250
using 1 thread
Specifying allele frequencies, mean: 0.508, sd: 0.281
MLE IBD: the sum of all selected genotypes (0,1,2) = 6317
MLE IBD: Fri Dec 20 06:13:28 2024 0%
MLE IBD: Fri Dec 20 06:13:29 2024 100%
IBD analysis (PLINK method of moment) on genotypes:
Excluding 8,838 SNPs (non-autosomes or non-selection)
Excluding 0 SNP (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 25
# of SNPs: 250
using 1 thread
Specifying allele frequencies, mean: 0.508, sd: 0.281
*** A correction factor based on allele count is not used, since the allele frequencies are specified.
PLINK IBD: the sum of all selected genotypes (0,1,2) = 6317
Fri Dec 20 06:13:29 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:29 2024 Done.
Genotype matrix: 250 SNPs X 25 samples
[1] -384.5064
[1] -379.8635
[1] -389.2882
[1] -390.0637
[1] -405.3267
[1] -386.6771
[1] -382.3052
[1] -375.7884
[1] -400.5859
[1] -379.9675
[1] -372.4947
[1] -372.3346
[1] -393.543
[1] -387.7755
[1] -373.858
[1] -380.4349
[1] -389.0108
[1] -402.2013
[1] -393.1451
[1] -388.5999
[1] -383.8134
[1] -376.6837
[1] -385.4354
[1] -378.9947
FUNCTION: snpgdsPairScore
Excluding 365 SNPs on non-autosomes
Pair Score Calculation:
# of samples: 120
# of SNPs: 8,723
Method: IBS
Genotype Score: the sum of all selected genotypes (0,1,2) = 1050236
List of 3
$ sample.id: chr [1:120] "NA19139" "NA19160" "NA07034" "NA12814" ...
$ snp.id : int [1:8723] 1 2 3 4 5 6 7 8 9 10 ...
$ score :'data.frame': 60 obs. of 5 variables:
..$ Avg : num [1:60] 1.72 1.73 1.71 1.72 1.73 ...
..$ SD : num [1:60] 0.452 0.443 0.457 0.45 0.443 ...
..$ Num : int [1:60] 8684 8627 8669 8637 8682 8634 8654 8678 8680 8679 ...
..$ Sample1: chr [1:60] "NA19139" "NA10847" "NA18515" "NA19129" ...
..$ Sample2: chr [1:60] "NA19138" "NA12146" "NA18516" "NA19128" ...
Pair Score Calculation:
# of samples: 120
# of SNPs: 8,723
Method: IBS
Genotype Score: the sum of all selected genotypes (0,1,2) = 1050236
List of 3
$ sample.id: chr [1:120] "NA19139" "NA19160" "NA07034" "NA12814" ...
$ snp.id : int [1:8723] 1 2 3 4 5 6 7 8 9 10 ...
$ score :'data.frame': 60 obs. of 5 variables:
..$ Avg : num [1:60] 0.999 1 1 1 1 ...
..$ SD : num [1:60] 0.024 0 0.0186 0.0215 0.0215 ...
..$ Num : int [1:60] 8684 8627 8669 8637 8682 8634 8654 8678 8680 8679 ...
..$ Sample1: chr [1:60] "NA19139" "NA10847" "NA18515" "NA19129" ...
..$ Sample2: chr [1:60] "NA19138" "NA12146" "NA18516" "NA19128" ...
Pair Score Calculation:
# of samples: 120
# of SNPs: 8,723
Method: IBS
Genotype Score: the sum of all selected genotypes (0,1,2) = 1050236
List of 3
$ sample.id: chr [1:120] "NA19139" "NA19160" "NA07034" "NA12814" ...
$ snp.id : int [1:8723] 1 2 3 4 5 6 7 8 9 10 ...
$ score : num [1:3, 1:8723] 1.75 0.437 60 1.583 0.497 ...
..- attr(*, "dimnames")=List of 2
.. ..$ : chr [1:3] "Avg" "SD" "Num"
.. ..$ : NULL
Pair Score Calculation:
# of samples: 120
# of SNPs: 8,723
Method: IBS
Genotype Score: the sum of all selected genotypes (0,1,2) = 1050236
List of 3
$ sample.id: chr [1:120] "NA19139" "NA19160" "NA07034" "NA12814" ...
$ snp.id : int [1:8723] 1 2 3 4 5 6 7 8 9 10 ...
$ score : int [1:60, 1:8723] 1 1 2 2 2 2 2 1 2 2 ...
Pair Score Calculation:
# of samples: 120
# of SNPs: 8,723
Method: IBS
Output: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\tmp.gds
Genotype Score: the sum of all selected genotypes (0,1,2) = 1050236
FUNCTION: snpgdsSNPList
FUNCTION: snpgdsSNPListClass
FUNCTION: snpgdsSNPListIntersect
FUNCTION: snpgdsSNPRateFreq
FUNCTION: snpgdsSampMissRate
FUNCTION: snpgdsSelectSNP
Excluding 365 SNPs on non-autosomes
Excluding 1,221 SNPs (monomorphic: TRUE, MAF: 0.05, missing rate: 0.95)
FUNCTION: snpgdsSlidingWindow
Sliding Window Analysis:
Excluding 8 SNPs (monomorphic: TRUE, MAF: NaN, missing rate: NaN)
# of samples: 279
# of SNPs: 9,080
using 1 thread
window size: 500000, shift: 100000 (basepair)
Chromosome Set: 1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23
Fri Dec 20 06:13:30 2024, Chromosome 1 (716 SNPs), 2448 windows
Fri Dec 20 06:13:30 2024, Chromosome 2 (742 SNPs), 2416 windows
Fri Dec 20 06:13:30 2024, Chromosome 3 (609 SNPs), 1985 windows
Fri Dec 20 06:13:31 2024, Chromosome 4 (562 SNPs), 1894 windows
Fri Dec 20 06:13:31 2024, Chromosome 5 (566 SNPs), 1797 windows
Fri Dec 20 06:13:31 2024, Chromosome 6 (565 SNPs), 1694 windows
Fri Dec 20 06:13:31 2024, Chromosome 7 (472 SNPs), 1573 windows
Fri Dec 20 06:13:31 2024, Chromosome 8 (488 SNPs), 1445 windows
Fri Dec 20 06:13:31 2024, Chromosome 9 (416 SNPs), 1393 windows
Fri Dec 20 06:13:31 2024, Chromosome 10 (483 SNPs), 1343 windows
Fri Dec 20 06:13:31 2024, Chromosome 11 (447 SNPs), 1338 windows
Fri Dec 20 06:13:31 2024, Chromosome 12 (427 SNPs), 1316 windows
Fri Dec 20 06:13:31 2024, Chromosome 13 (344 SNPs), 948 windows
Fri Dec 20 06:13:31 2024, Chromosome 14 (281 SNPs), 847 windows
Fri Dec 20 06:13:31 2024, Chromosome 15 (262 SNPs), 774 windows
Fri Dec 20 06:13:31 2024, Chromosome 16 (278 SNPs), 873 windows
Fri Dec 20 06:13:31 2024, Chromosome 17 (207 SNPs), 773 windows
Fri Dec 20 06:13:31 2024, Chromosome 18 (266 SNPs), 753 windows
Fri Dec 20 06:13:31 2024, Chromosome 19 (120 SNPs), 627 windows
Fri Dec 20 06:13:31 2024, Chromosome 20 (229 SNPs), 602 windows
Fri Dec 20 06:13:31 2024, Chromosome 21 (126 SNPs), 311 windows
Fri Dec 20 06:13:31 2024, Chromosome 22 (116 SNPs), 312 windows
Fri Dec 20 06:13:31 2024, Chromosome 23 (358 SNPs), 1507 windows
Fri Dec 20 06:13:31 2024 Done.
FUNCTION: snpgdsSummary
The file name: F:\biocbuild\bbs-3.20-bioc\R\library\SNPRelate\extdata\hapmap_geno.gds
The total number of samples: 279
The total number of SNPs: 9088
SNP genotypes are stored in SNP-major mode (Sample X SNP).
FUNCTION: snpgdsTranspose
The file name: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\test.gds
The total number of samples: 279
The total number of SNPs: 9088
SNP genotypes are stored in SNP-major mode (Sample X SNP).
SNP genotypes: 279 samples, 9088 SNPs
Genotype matrix is being transposed ...
Clean up the fragments of GDS file:
open the file 'test.gds' (1.3M)
# of fragments: 28
save to 'test.gds.tmp'
rename 'test.gds.tmp' (709.6K, reduced: 619.1K)
# of fragments: 26
The file name: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\test.gds
The total number of samples: 279
The total number of SNPs: 9088
SNP genotypes are stored in individual-major mode (SNP X Sample).
FUNCTION: snpgdsVCF2GDS
##fileformat=VCFv4.1
##fileDate=20090805
##source=myImputationProgramV3.1
##reference=file:///seq/references/1000GenomesPilot-NCBI36.fasta
##contig=<ID=20,length=62435964,assembly=B36,md5=f126cdf8a6e0c7f379d618ff66beb2da,species="Homo sapiens",taxonomy=x>
##phasing=partial
##INFO=<ID=NS,Number=1,Type=Integer,Description="Number of Samples With Data">
##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth">
##INFO=<ID=AF,Number=A,Type=Float,Description="Allele Frequency">
##INFO=<ID=AA,Number=1,Type=String,Description="Ancestral Allele">
##INFO=<ID=DB,Number=0,Type=Flag,Description="dbSNP membership, build 129">
##INFO=<ID=H2,Number=0,Type=Flag,Description="HapMap2 membership">
##FILTER=<ID=q10,Description="Quality below 10">
##FILTER=<ID=s50,Description="Less than 50% of samples have data">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
##FORMAT=<ID=HQ,Number=2,Type=Integer,Description="Haplotype Quality">
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT NA00001 NA00002 NA00003
20 14370 rs6054257 G A 29 PASS NS=3;DP=14;AF=0.5;DB;H2 GT:GQ:DP:HQ 0|0:48:1:51,51 1|0:48:8:51,51 1/1:43:5:.,.
20 17330 . T A 3 q10 NS=3;DP=11;AF=0.017 GT:GQ:DP:HQ 0|0:49:3:58,50 0|1:3:5:65,3 0/0:41:3
20 1110696 rs6040355 A G,T 67 PASS NS=2;DP=10;AF=0.333,0.667;AA=T;DB GT:GQ:DP:HQ 1|2:21:6:23,27 2|1:2:0:18,2 2/2:35:4
20 1230237 . T . 47 PASS NS=3;DP=13;AA=T GT:GQ:DP:HQ 0|0:54:7:56,60 0|0:48:4:51,51 0/0:61:2
20 1234567 microsat1 GTC G,GTCT 50 PASS NS=3;DP=9;AA=G GT:GQ:DP 0/1:35:4 0/2:17:2 1/1:40:3
Start file conversion from VCF to SNP GDS ...
Method: extracting biallelic SNPs
Number of samples: 3
Parsing "F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf" ...
import 2 variants.
+ genotype { Bit2 3x2, 2B } *
Optimize the access efficiency ...
Clean up the fragments of GDS file:
open the file 'test1.gds' (2.9K)
# of fragments: 46
save to 'test1.gds.tmp'
rename 'test1.gds.tmp' (2.6K, reduced: 312B)
# of fragments: 20
The file name: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\test1.gds
The total number of samples: 3
The total number of SNPs: 2
SNP genotypes are stored in SNP-major mode (Sample X SNP).
Start file conversion from VCF to SNP GDS ...
Method: extracting biallelic SNPs
Number of samples: 3
Parsing "F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf" ...
import 2 variants.
+ genotype { Bit2 3x2, 2B } *
SNP genotypes: 3 samples, 2 SNPs
Genotype matrix is being transposed ...
Optimize the access efficiency ...
Clean up the fragments of GDS file:
open the file 'test2.gds' (3.0K)
# of fragments: 48
save to 'test2.gds.tmp'
rename 'test2.gds.tmp' (2.6K, reduced: 417B)
# of fragments: 20
The file name: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\test2.gds
The total number of samples: 3
The total number of SNPs: 2
SNP genotypes are stored in individual-major mode (SNP X Sample).
Start file conversion from VCF to SNP GDS ...
Method: dosage (0,1,2) of reference allele for all variant sites
Number of samples: 3
Parsing "F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf" ...
import 5 variants.
+ genotype { Bit2 3x5, 4B } *
SNP genotypes: 3 samples, 5 SNPs
Genotype matrix is being transposed ...
Optimize the access efficiency ...
Clean up the fragments of GDS file:
open the file 'test3.gds' (3.1K)
# of fragments: 48
save to 'test3.gds.tmp'
rename 'test3.gds.tmp' (2.7K, reduced: 419B)
# of fragments: 20
Some of 'snp.allele' are not standard (e.g., A/G,T).
The file name: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\test3.gds
The total number of samples: 3
The total number of SNPs: 5
SNP genotypes are stored in individual-major mode (SNP X Sample).
The number of valid samples: 3
The number of biallelic unique SNPs: 2
Start file conversion from VCF to SNP GDS ...
Method: dosage (0,1,2) of reference allele for all variant sites
Number of samples: 3
Parsing "F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf" ...
import 5 variants.
+ genotype { Bit2 3x5, 4B } *
Optimize the access efficiency ...
Clean up the fragments of GDS file:
open the file 'test4.gds' (3.0K)
# of fragments: 46
save to 'test4.gds.tmp'
rename 'test4.gds.tmp' (2.7K, reduced: 312B)
# of fragments: 20
Some of 'snp.allele' are not standard (e.g., A/G,T).
The file name: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\test4.gds
The total number of samples: 3
The total number of SNPs: 5
SNP genotypes are stored in SNP-major mode (Sample X SNP).
The number of valid samples: 3
The number of biallelic unique SNPs: 2
Start file conversion from VCF to SNP GDS ...
Method: dosage (0,1,2) of reference allele for all variant sites
Number of samples: 3
Parsing "F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf" ...
import 5 variants.
+ genotype { Bit2 3x5, 4B } *
Optimize the access efficiency ...
Clean up the fragments of GDS file:
open the file 'test5.gds' (3.0K)
# of fragments: 46
save to 'test5.gds.tmp'
rename 'test5.gds.tmp' (2.7K, reduced: 312B)
# of fragments: 20
Some of 'snp.allele' are not standard (e.g., T/A,G).
The file name: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\test5.gds
The total number of samples: 3
The total number of SNPs: 5
SNP genotypes are stored in SNP-major mode (Sample X SNP).
The number of valid samples: 3
The number of biallelic unique SNPs: 2
FUNCTION: snpgdsVCF2GDS_R
##fileformat=VCFv4.1
##fileDate=20090805
##source=myImputationProgramV3.1
##reference=file:///seq/references/1000GenomesPilot-NCBI36.fasta
##contig=<ID=20,length=62435964,assembly=B36,md5=f126cdf8a6e0c7f379d618ff66beb2da,species="Homo sapiens",taxonomy=x>
##phasing=partial
##INFO=<ID=NS,Number=1,Type=Integer,Description="Number of Samples With Data">
##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth">
##INFO=<ID=AF,Number=A,Type=Float,Description="Allele Frequency">
##INFO=<ID=AA,Number=1,Type=String,Description="Ancestral Allele">
##INFO=<ID=DB,Number=0,Type=Flag,Description="dbSNP membership, build 129">
##INFO=<ID=H2,Number=0,Type=Flag,Description="HapMap2 membership">
##FILTER=<ID=q10,Description="Quality below 10">
##FILTER=<ID=s50,Description="Less than 50% of samples have data">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
##FORMAT=<ID=HQ,Number=2,Type=Integer,Description="Haplotype Quality">
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT NA00001 NA00002 NA00003
20 14370 rs6054257 G A 29 PASS NS=3;DP=14;AF=0.5;DB;H2 GT:GQ:DP:HQ 0|0:48:1:51,51 1|0:48:8:51,51 1/1:43:5:.,.
20 17330 . T A 3 q10 NS=3;DP=11;AF=0.017 GT:GQ:DP:HQ 0|0:49:3:58,50 0|1:3:5:65,3 0/0:41:3
20 1110696 rs6040355 A G,T 67 PASS NS=2;DP=10;AF=0.333,0.667;AA=T;DB GT:GQ:DP:HQ 1|2:21:6:23,27 2|1:2:0:18,2 2/2:35:4
20 1230237 . T . 47 PASS NS=3;DP=13;AA=T GT:GQ:DP:HQ 0|0:54:7:56,60 0|0:48:4:51,51 0/0:61:2
20 1234567 microsat1 GTC G,GTCT 50 PASS NS=3;DP=9;AA=G GT:GQ:DP 0/1:35:4 0/2:17:2 1/1:40:3
Start snpgdsVCF2GDS ...
Extracting bi-allelic and polymorhpic SNPs.
Scanning ...
file: F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf
content: 5 rows x 12 columns
Fri Dec 20 06:13:32 2024 store sample id, snp id, position, and chromosome.
start writing: 3 samples, 2 SNPs ...
file: F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf
[1] 1
Fri Dec 20 06:13:32 2024 Done.
The file name: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\test1.gds
The total number of samples: 3
The total number of SNPs: 2
SNP genotypes are stored in SNP-major mode (Sample X SNP).
Start snpgdsVCF2GDS ...
Extracting bi-allelic and polymorhpic SNPs.
Scanning ...
file: F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf
content: 5 rows x 12 columns
Fri Dec 20 06:13:32 2024 store sample id, snp id, position, and chromosome.
start writing: 3 samples, 2 SNPs ...
file: F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf
[1] 1
Fri Dec 20 06:13:32 2024 Done.
The file name: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\test2.gds
The total number of samples: 3
The total number of SNPs: 2
SNP genotypes are stored in SNP-major mode (Sample X SNP).
Start snpgdsVCF2GDS ...
Storing dosage of the reference allele for all variant sites, including bi-allelic SNPs, multi-allelic SNPs, indels and structural variants.
Scanning ...
file: F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf
content: 5 rows x 12 columns
Fri Dec 20 06:13:32 2024 store sample id, snp id, position, and chromosome.
start writing: 3 samples, 5 SNPs ...
file: F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf
Fri Dec 20 06:13:32 2024 Done.
Some of 'snp.allele' are not standard (e.g., A/G,T).
The file name: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\test3.gds
The total number of samples: 3
The total number of SNPs: 5
SNP genotypes are stored in SNP-major mode (Sample X SNP).
The number of valid samples: 3
The number of biallelic unique SNPs: 2
Start snpgdsVCF2GDS ...
Storing dosage of the reference allele for all variant sites, including bi-allelic SNPs, multi-allelic SNPs, indels and structural variants.
Scanning ...
file: F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf
content: 5 rows x 12 columns
Fri Dec 20 06:13:32 2024 store sample id, snp id, position, and chromosome.
start writing: 3 samples, 5 SNPs ...
file: F:/biocbuild/bbs-3.20-bioc/R/library/SNPRelate/extdata/sequence.vcf
Fri Dec 20 06:13:32 2024 Done.
Some of 'snp.allele' are not standard (e.g., A/G,T).
The file name: F:\biocbuild\bbs-3.20-bioc\meat\SNPRelate.Rcheck\tests\test4.gds
The total number of samples: 3
The total number of SNPs: 5
SNP genotypes are stored in SNP-major mode (Sample X SNP).
The number of valid samples: 3
The number of biallelic unique SNPs: 2
SNP Correlation:
# of samples: 90
# of SNPs: 9,088
using 1 thread
Correlation: the sum of all selected genotypes (0,1,2) = 824424
Fri Dec 20 06:13:34 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:34 2024 Done.
SNP Correlation:
# of samples: 90
# of SNPs: 9,088
using 1 thread
Creating 'test.gds' ...
Correlation: the sum of all selected genotypes (0,1,2) = 824424
Fri Dec 20 06:13:34 2024
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:34 2024 Done.
SNP Loading:
# of samples: 90
# of SNPs: 8,695
using 1 thread
using the top 8 eigenvectors
SNP Loading: the sum of all selected genotypes (0,1,2) = 787449
Fri Dec 20 06:13:34 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:34 2024 Done.
Sample Loading:
# of samples: 100
# of SNPs: 8,695
using 1 thread
using the top 8 eigenvectors
Sample Loading: the sum of all selected genotypes (0,1,2) = 875255
Fri Dec 20 06:13:34 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:34 2024 Done.
SNP Correlation:
# of samples: 90
# of SNPs: 9,088
using 2 threads
Correlation: the sum of all selected genotypes (0,1,2) = 824424
Fri Dec 20 06:13:34 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:34 2024 Done.
SNP Correlation:
# of samples: 90
# of SNPs: 9,088
using 2 threads
Creating 'test.gds' ...
Correlation: the sum of all selected genotypes (0,1,2) = 824424
Fri Dec 20 06:13:34 2024
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:34 2024 Done.
SNP Loading:
# of samples: 90
# of SNPs: 8,695
using 1 thread
using the top 8 eigenvectors
SNP Loading: the sum of all selected genotypes (0,1,2) = 787449
Fri Dec 20 06:13:35 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:35 2024 Done.
Sample Loading:
# of samples: 100
# of SNPs: 8,695
using 1 thread
using the top 8 eigenvectors
Sample Loading: the sum of all selected genotypes (0,1,2) = 875255
Fri Dec 20 06:13:35 2024 (internal increment: 65536)
[..................................................] 0%, ETC: ---
[==================================================] 100%, completed, 0s
Fri Dec 20 06:13:35 2024 Done.
RUNIT TEST PROTOCOL -- Fri Dec 20 06:13:35 2024
***********************************************
Number of test functions: 13
Number of errors: 0
Number of failures: 0
1 Test Suite :
SNPRelate RUnit Tests - 13 test functions, 0 errors, 0 failures
Number of test functions: 13
Number of errors: 0
Number of failures: 0
>
> proc.time()
user system elapsed
47.87 3.67 53.42
SNPRelate.Rcheck/SNPRelate-Ex.timings
| name | user | system | elapsed | |
| SNPGDSFileClass-class | 0.05 | 0.02 | 0.06 | |
| SNPRelate-package | 1.41 | 0.14 | 1.58 | |
| snpgdsAdmixPlot | 0.86 | 0.03 | 0.89 | |
| snpgdsAdmixProp | 0.74 | 0.02 | 0.75 | |
| snpgdsAlleleSwitch | 0.08 | 0.03 | 0.11 | |
| snpgdsApartSelection | 0.07 | 0.01 | 0.09 | |
| snpgdsBED2GDS | 0.13 | 0.04 | 0.19 | |
| snpgdsClose | 0.04 | 0.00 | 0.04 | |
| snpgdsCombineGeno | 0.17 | 0.01 | 0.37 | |
| snpgdsCreateGeno | 0.79 | 0.05 | 0.86 | |
| snpgdsCreateGenoSet | 0.24 | 0.05 | 0.30 | |
| snpgdsCutTree | 2.19 | 0.15 | 2.34 | |
| snpgdsDiss | 1.89 | 0.03 | 1.92 | |
| snpgdsDrawTree | 1.64 | 0.02 | 1.66 | |
| snpgdsEIGMIX | 0.75 | 0.03 | 0.78 | |
| snpgdsErrMsg | 0 | 0 | 0 | |
| snpgdsExampleFileName | 0 | 0 | 0 | |
| snpgdsFst | 0.03 | 0.00 | 0.03 | |
| snpgdsGDS2BED | 0.11 | 0.00 | 0.13 | |
| snpgdsGDS2Eigen | 0.23 | 0.03 | 0.26 | |
| snpgdsGDS2PED | 0.46 | 0.06 | 0.52 | |
| snpgdsGEN2GDS | 0 | 0 | 0 | |
| snpgdsGRM | 1.85 | 0.11 | 1.97 | |
| snpgdsGetGeno | 0.04 | 0.03 | 0.06 | |
| snpgdsHCluster | 1.79 | 0.04 | 1.83 | |
| snpgdsHWE | 0.02 | 0.01 | 0.03 | |
| snpgdsIBDKING | 1.94 | 0.03 | 1.97 | |
| snpgdsIBDMLE | 1.21 | 0.05 | 1.26 | |
| snpgdsIBDMLELogLik | 1.16 | 0.00 | 1.16 | |
| snpgdsIBDMoM | 0.44 | 0.00 | 0.44 | |
| snpgdsIBDSelection | 0.17 | 0.00 | 0.17 | |
| snpgdsIBS | 0.28 | 0.00 | 0.28 | |
| snpgdsIBSNum | 0.38 | 0.01 | 0.39 | |
| snpgdsIndInb | 0.18 | 0.00 | 0.19 | |
| snpgdsIndInbCoef | 0 | 0 | 0 | |
| snpgdsIndivBeta | 0.21 | 0.02 | 0.22 | |
| snpgdsLDMat | 0.33 | 0.00 | 0.32 | |
| snpgdsLDpair | 0 | 0 | 0 | |
| snpgdsLDpruning | 0.06 | 0.00 | 0.07 | |
| snpgdsMergeGRM | 3.00 | 0.19 | 3.26 | |
| snpgdsOpen | 0.04 | 0.00 | 0.05 | |
| snpgdsOption | 0 | 0 | 0 | |
| snpgdsPCA | 0.93 | 0.00 | 0.92 | |
| snpgdsPCACorr | 0.93 | 0.11 | 1.06 | |
| snpgdsPCASNPLoading | 0.86 | 0.04 | 0.91 | |
| snpgdsPCASampLoading | 0.84 | 0.05 | 0.98 | |
| snpgdsPED2GDS | 1.00 | 0.11 | 1.16 | |
| snpgdsPairIBD | 1.44 | 0.00 | 1.43 | |
| snpgdsPairIBDMLELogLik | 0.8 | 0.0 | 0.8 | |
| snpgdsPairScore | 0.18 | 0.14 | 0.34 | |
| snpgdsSNPList | 0.02 | 0.00 | 0.02 | |
| snpgdsSNPListIntersect | 0.09 | 0.00 | 0.09 | |
| snpgdsSNPRateFreq | 0.18 | 0.00 | 0.18 | |
| snpgdsSampMissRate | 0.01 | 0.00 | 0.01 | |
| snpgdsSelectSNP | 0.02 | 0.00 | 0.02 | |
| snpgdsSlidingWindow | 0.95 | 0.20 | 1.16 | |
| snpgdsSummary | 0.05 | 0.00 | 0.05 | |
| snpgdsTranspose | 0.11 | 0.03 | 0.26 | |
| snpgdsVCF2GDS | 0.14 | 0.25 | 0.65 | |
| snpgdsVCF2GDS_R | 0.03 | 0.09 | 0.21 | |