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HostnameOSArch (*)R versionInstalled pkgs
nebbiolo1Linux (Ubuntu 24.04.1 LTS)x86_64R Under development (unstable) (2025-01-20 r87609) -- "Unsuffered Consequences" 4658
palomino7Windows Server 2022 Datacenterx64R Under development (unstable) (2025-01-21 r87610 ucrt) -- "Unsuffered Consequences" 4455
kunpeng2Linux (openEuler 22.03 LTS-SP1)aarch64R Under development (unstable) (2024-11-24 r87369) -- "Unsuffered Consequences" 4408
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Package 711/2286HostnameOS / ArchINSTALLBUILDCHECKBUILD BIN
FindIT2 1.13.0  (landing page)
Guandong Shang
Snapshot Date: 2025-01-24 13:40 -0500 (Fri, 24 Jan 2025)
git_url: https://git.bioconductor.org/packages/FindIT2
git_branch: devel
git_last_commit: 30235ec
git_last_commit_date: 2024-10-29 11:01:40 -0500 (Tue, 29 Oct 2024)
nebbiolo1Linux (Ubuntu 24.04.1 LTS) / x86_64  OK    OK    OK  UNNEEDED, same version is already published
palomino7Windows Server 2022 Datacenter / x64  OK    OK    OK    OK  UNNEEDED, same version is already published
kunpeng2Linux (openEuler 22.03 LTS-SP1) / aarch64  OK    OK    OK  


CHECK results for FindIT2 on kunpeng2

To the developers/maintainers of the FindIT2 package:
- Allow up to 24 hours (and sometimes 48 hours) for your latest push to git@git.bioconductor.org:packages/FindIT2.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.
- See Martin Grigorov's blog post for how to debug Linux ARM64 related issues on a x86_64 host.

raw results


Summary

Package: FindIT2
Version: 1.13.0
Command: /home/biocbuild/R/R/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/home/biocbuild/R/R/site-library --no-vignettes --timings FindIT2_1.13.0.tar.gz
StartedAt: 2025-01-25 06:57:35 -0000 (Sat, 25 Jan 2025)
EndedAt: 2025-01-25 07:05:29 -0000 (Sat, 25 Jan 2025)
EllapsedTime: 473.5 seconds
RetCode: 0
Status:   OK  
CheckDir: FindIT2.Rcheck
Warnings: 0

Command output

##############################################################################
##############################################################################
###
### Running command:
###
###   /home/biocbuild/R/R/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/home/biocbuild/R/R/site-library --no-vignettes --timings FindIT2_1.13.0.tar.gz
###
##############################################################################
##############################################################################


* using log directory ‘/home/biocbuild/bbs-3.21-bioc/meat/FindIT2.Rcheck’
* using R Under development (unstable) (2024-11-24 r87369)
* using platform: aarch64-unknown-linux-gnu
* R was compiled by
    aarch64-unknown-linux-gnu-gcc (GCC) 14.2.0
    GNU Fortran (GCC) 14.2.0
* running under: openEuler 24.03 (LTS)
* using session charset: UTF-8
* using option ‘--no-vignettes’
* checking for file ‘FindIT2/DESCRIPTION’ ... OK
* this is package ‘FindIT2’ version ‘1.13.0’
* package encoding: UTF-8
* checking package namespace information ... OK
* checking package dependencies ... INFO
Imports includes 22 non-default packages.
Importing from so many packages makes the package vulnerable to any of
them becoming unavailable.  Move as many as possible to Suggests and
use conditionally.
* checking if this is a source package ... OK
* checking if there is a namespace ... OK
* checking for hidden files and directories ... OK
* checking for portable file names ... OK
* checking for sufficient/correct file permissions ... OK
* checking whether package ‘FindIT2’ can be installed ... OK
* checking installed package size ... OK
* checking package directory ... OK
* checking ‘build’ directory ... OK
* checking DESCRIPTION meta-information ... OK
* checking top-level files ... OK
* checking for left-over files ... OK
* checking index information ... OK
* checking package subdirectories ...Warning: program compiled against libxml 212 using older 211
 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 loading without being on the library search path ... OK
* checking dependencies in R code ... OK
* checking S3 generic/method consistency ... OK
* checking replacement functions ... OK
* checking foreign function calls ... OK
* checking R code for possible problems ... OK
* checking Rd files ... OK
* checking Rd metadata ... OK
* checking Rd cross-references ... OK
* checking for missing documentation entries ... OK
* checking for code/documentation mismatches ... OK
* checking Rd \usage sections ... OK
* checking Rd contents ... OK
* checking for unstated dependencies in examples ... OK
* checking contents of ‘data’ directory ... OK
* checking data for non-ASCII characters ... OK
* checking data for ASCII and uncompressed saves ... OK
* checking files in ‘vignettes’ ... OK
* checking examples ... OK
Examples with CPU (user + system) or elapsed time > 5s
                 user system elapsed
calcRP_coverage 8.558  0.172   8.745
findIT_regionRP 8.258  0.220   8.492
calcRP_region   6.793  0.192   7.001
calcRP_TFHit    4.779  0.203   5.142
* checking for unstated dependencies in ‘tests’ ... OK
* checking tests ...
  Running ‘testthat.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: OK


Installation output

FindIT2.Rcheck/00install.out

##############################################################################
##############################################################################
###
### Running command:
###
###   /home/biocbuild/R/R/bin/R CMD INSTALL FindIT2
###
##############################################################################
##############################################################################


* installing to library ‘/home/biocbuild/R/R-4.5.0-devel_2024-11-24/site-library’
* installing *source* package ‘FindIT2’ ...
** using staged installation
** R
** data
** inst
** byte-compile and prepare package for lazy loading
** help
*** installing help indices
** building package indices
** installing vignettes
** testing if installed package can be loaded from temporary location
** testing if installed package can be loaded from final location
** testing if installed package keeps a record of temporary installation path
* DONE (FindIT2)

Tests output

FindIT2.Rcheck/tests/testthat.Rout


R Under development (unstable) (2024-11-24 r87369) -- "Unsuffered Consequences"
Copyright (C) 2024 The R Foundation for Statistical Computing
Platform: aarch64-unknown-linux-gnu

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

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

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

> library(testthat)
> library(FindIT2)
Loading required package: GenomicRanges
Loading required package: stats4
Loading required package: BiocGenerics
Loading required package: generics

Attaching package: 'generics'

The following objects are masked from 'package:base':

    as.difftime, as.factor, as.ordered, intersect, is.element, setdiff,
    setequal, union


Attaching package: 'BiocGenerics'

The following objects are masked from 'package:stats':

    IQR, mad, sd, var, xtabs

The following objects are masked from 'package:base':

    Filter, Find, Map, Position, Reduce, anyDuplicated, aperm, append,
    as.data.frame, basename, cbind, colnames, dirname, do.call,
    duplicated, eval, evalq, get, grep, grepl, is.unsorted, lapply,
    mapply, match, mget, order, paste, pmax, pmax.int, pmin, pmin.int,
    rank, rbind, rownames, sapply, saveRDS, table, tapply, unique,
    unsplit, which.max, which.min

Loading required package: S4Vectors

Attaching package: 'S4Vectors'

The following object is masked from 'package:utils':

    findMatches

The following objects are masked from 'package:base':

    I, expand.grid, unname

Loading required package: IRanges
Loading required package: GenomeInfoDb
> if (!requireNamespace("TxDb.Athaliana.BioMart.plantsmart28")) {
+     stop("unable to load TxDb.Athaliana.BioMart.plantsmart28")
+ }
Loading required namespace: TxDb.Athaliana.BioMart.plantsmart28
> 
> test_check("FindIT2")
>> preparing gene features information...		2025-01-25 07:04:09
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:04:10
>> preparing weight info...		2025-01-25 07:04:10
>> loading E50h_sampleChr5.bw info...		2025-01-25 07:04:10
------------
>> extracting and calcluating Chr5 signal...		2025-01-25 07:04:10
>> dealing with Chr5 left gene signal...		2025-01-25 07:04:18
>> norming Chr5RP accoring to the whole Chr RP...		2025-01-25 07:04:18
>> merging all Chr RP together...		2025-01-25 07:04:18
>> done		2025-01-25 07:04:18
>> checking seqlevels match...		2025-01-25 07:04:18
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2025-01-25 07:04:18
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:04:19
>> finding overlap peak in gene scan region...		2025-01-25 07:04:19
>> dealing with left peak not your gene scan region...		2025-01-25 07:04:20
>> merging two set peaks...		2025-01-25 07:04:20
>> calculating distance and dealing with gene strand...		2025-01-25 07:04:20
>> merging all info together ...		2025-01-25 07:04:20
>> done		2025-01-25 07:04:20
>> calculating peakCenter to TSS using peak-gene pair...		2025-01-25 07:04:20
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2025-01-25 07:04:21
>> calculating RP using centerToTSS and peak score2025-01-25 07:04:21
>> merging all info together		2025-01-25 07:04:24
>> done		2025-01-25 07:04:25
>> calculating peakCenter to TSS using peak-gene pair...		2025-01-25 07:04:25
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2025-01-25 07:04:26
>> calculating RP using centerToTSS and peak score2025-01-25 07:04:26
>> merging all info together		2025-01-25 07:04:30
>> done		2025-01-25 07:04:31
>> checking seqlevels match...		2025-01-25 07:04:31
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2025-01-25 07:04:31
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:04:32
>> finding overlap peak in gene scan region...		2025-01-25 07:04:32
>> dealing with left peak not your gene scan region...		2025-01-25 07:04:32
>> merging two set peaks...		2025-01-25 07:04:32
>> calculating distance and dealing with gene strand...		2025-01-25 07:04:32
>> merging all info together ...		2025-01-25 07:04:33
>> done		2025-01-25 07:04:33
>> calculating peakCenter to TSS using peak-gene pair...		2025-01-25 07:04:33
>> calculating RP using centerToTSS and TF hit		2025-01-25 07:04:34
>> merging all info together		2025-01-25 07:04:34
>> done		2025-01-25 07:04:34
>> calculating peakCenter to TSS using peak-gene pair...		2025-01-25 07:04:34
>> calculating RP using centerToTSS and TF hit		2025-01-25 07:04:35
>> merging all info together		2025-01-25 07:04:35
>> done		2025-01-25 07:04:35
>> checking seqlevels match...		2025-01-25 07:04:36
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2025-01-25 07:04:36
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:04:38
>> finding overlap peak in gene scan region...		2025-01-25 07:04:38
>> dealing with left peak not your gene scan region...		2025-01-25 07:04:38
>> merging two set peaks...		2025-01-25 07:04:38
>> calculating distance and dealing with gene strand...		2025-01-25 07:04:38
>> merging all info together ...		2025-01-25 07:04:38
>> done		2025-01-25 07:04:38
>> calculating peakCenter to TSS using peak-gene pair...		2025-01-25 07:04:38
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2025-01-25 07:04:39
>> calculating RP using centerToTSS and peak score2025-01-25 07:04:39
>> merging all info together		2025-01-25 07:04:42
>> done		2025-01-25 07:04:43
>> extracting RP info from regionRP...		2025-01-25 07:04:43
>> dealing with TF_GR_databse...		2025-01-25 07:04:44
>> calculating percent and p-value...		2025-01-25 07:04:44
>> dealing withE5_0h_R1...		2025-01-25 07:04:44
>> dealing withE5_0h_R2...		2025-01-25 07:04:44
>> dealing withE5_4h_R1...		2025-01-25 07:04:44
>> dealing withE5_4h_R2...		2025-01-25 07:04:44
>> dealing withE5_8h_R1...		2025-01-25 07:04:44
>> dealing withE5_8h_R2...		2025-01-25 07:04:44
>> dealing withE5_16h_R1...		2025-01-25 07:04:44
>> dealing withE5_16h_R2...		2025-01-25 07:04:44
>> dealing withE5_24h_R1...		2025-01-25 07:04:44
>> dealing withE5_24h_R2...		2025-01-25 07:04:44
>> dealing withE5_48h_R1...		2025-01-25 07:04:44
>> dealing withE5_48h_R2...		2025-01-25 07:04:44
>> dealing withE5_48h_R3...		2025-01-25 07:04:44
>> dealing withE5_72h_R1...		2025-01-25 07:04:44
>> dealing withE5_72h_R2...		2025-01-25 07:04:45
>> dealing withE5_72h_R3...		2025-01-25 07:04:45
>> merging all info together...		2025-01-25 07:04:45
>> done		2025-01-25 07:04:45
>> preparing gene features information...		2025-01-25 07:04:45
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:04:46
>> calculating p-value for each TF, which may be time consuming...		2025-01-25 07:04:46
>> merging all info together...		2025-01-25 07:04:46
>> done		2025-01-25 07:04:46
>> dealing with TF_GR_database...		2025-01-25 07:04:46
>> calculating coef and converting into z-score using INT...		2025-01-25 07:04:47
>> dealing with E5_0h_R1...		2025-01-25 07:04:47
>> dealing with E5_0h_R2...		2025-01-25 07:04:47
>> dealing with E5_4h_R1...		2025-01-25 07:04:47
>> dealing with E5_4h_R2...		2025-01-25 07:04:47
>> dealing with E5_8h_R1...		2025-01-25 07:04:47
>> dealing with E5_8h_R2...		2025-01-25 07:04:47
>> dealing with E5_16h_R1...		2025-01-25 07:04:47
>> dealing with E5_16h_R2...		2025-01-25 07:04:47
>> dealing with E5_24h_R1...		2025-01-25 07:04:47
>> dealing with E5_24h_R2...		2025-01-25 07:04:47
>> dealing with E5_48h_R1...		2025-01-25 07:04:48
>> dealing with E5_48h_R2...		2025-01-25 07:04:48
>> dealing with E5_48h_R3...		2025-01-25 07:04:48
>> dealing with E5_72h_R1...		2025-01-25 07:04:48
>> dealing with E5_72h_R2...		2025-01-25 07:04:48
>> dealing with E5_72h_R3...		2025-01-25 07:04:48
>> merging all info together...		2025-01-25 07:04:48
>> done		2025-01-25 07:04:48
>> checking seqlevels match...		2025-01-25 07:04:49
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2025-01-25 07:04:49
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:04:50
>> finding overlap peak in gene scan region...		2025-01-25 07:04:50
>> dealing with left peak not your gene scan region...		2025-01-25 07:04:50
>> merging two set peaks...		2025-01-25 07:04:50
>> calculating distance and dealing with gene strand...		2025-01-25 07:04:50
>> merging all info together ...		2025-01-25 07:04:50
>> done		2025-01-25 07:04:50
>> calculating peakCenter to TSS using peak-gene pair...		2025-01-25 07:04:50
>> calculating RP using centerToTSS and TF hit		2025-01-25 07:04:51
>> merging all info together		2025-01-25 07:04:51
>> done		2025-01-25 07:04:51
>> checking seqlevels match...		2025-01-25 07:04:51
>> your peak_GR seqlevel:5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match...		2025-01-25 07:04:52
>> your peak_GR seqlevel:Chr5 Chr6...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match...		2025-01-25 07:04:56
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2025-01-25 07:04:56
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2025-01-25 07:04:56
>> finding nearest gene and calculating distance...		2025-01-25 07:04:57
>> dealing with gene strand ...		2025-01-25 07:04:57
>> merging all info together ...		2025-01-25 07:04:57
>> done		2025-01-25 07:04:57
>> checking seqlevels match...		2025-01-25 07:04:57
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2025-01-25 07:04:57
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2025-01-25 07:04:57
>> finding nearest gene and calculating distance...		2025-01-25 07:04:58
>> dealing with gene strand ...		2025-01-25 07:04:59
>> merging all info together ...		2025-01-25 07:04:59
>> done		2025-01-25 07:04:59
>> checking seqlevels match...		2025-01-25 07:05:00
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2025-01-25 07:05:00
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2025-01-25 07:05:00
>> finding nearest gene and calculating distance...		2025-01-25 07:05:01
>> dealing with gene strand ...		2025-01-25 07:05:01
>> merging all info together ...		2025-01-25 07:05:01
>> done		2025-01-25 07:05:01
>> checking seqlevels match...		2025-01-25 07:05:02
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2025-01-25 07:05:02
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2025-01-25 07:05:02
>> finding nearest gene and calculating distance...		2025-01-25 07:05:03
>> dealing with gene strand ...		2025-01-25 07:05:03
>> merging all info together ...		2025-01-25 07:05:03
>> done		2025-01-25 07:05:03
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match...		2025-01-25 07:05:05
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2025-01-25 07:05:05
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2025-01-25 07:05:05
>> finding nearest gene and calculating distance...		2025-01-25 07:05:06
>> dealing with gene strand ...		2025-01-25 07:05:06
>> merging all info together ...		2025-01-25 07:05:06
>> done		2025-01-25 07:05:06
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match...		2025-01-25 07:05:07
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2025-01-25 07:05:08
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:05:09
>> checking seqlevels match...		2025-01-25 07:05:10
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:05:11
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2025-01-25 07:05:13
>> merging all info together...		2025-01-25 07:05:13
>> done		2025-01-25 07:05:13
>> checking seqlevels match...		2025-01-25 07:05:13
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> using scanPromoter parameter to scan promoter for each gene...		2025-01-25 07:05:14
>> checking seqlevels match...		2025-01-25 07:05:14
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:05:15
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene...		2025-01-25 07:05:15
>> checking seqlevels match...		2025-01-25 07:05:15
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:05:16
>> calculating cor and pvalue, which may be time consuming...		2025-01-25 07:05:16
>> merging all info together...		2025-01-25 07:05:17
>> done		2025-01-25 07:05:17
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2025-01-25 07:05:17
>> merging all info together...		2025-01-25 07:05:17
>> done		2025-01-25 07:05:17
>> checking seqlevels match...		2025-01-25 07:05:17
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2025-01-25 07:05:17
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:05:18
>> finding overlap peak in gene scan region...		2025-01-25 07:05:18
>> dealing with left peak not your gene scan region...		2025-01-25 07:05:18
>> merging two set peaks...		2025-01-25 07:05:19
>> calculating distance and dealing with gene strand...		2025-01-25 07:05:19
>> merging all info together ...		2025-01-25 07:05:19
>> done		2025-01-25 07:05:19
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2025-01-25 07:05:20
>> merging all info together...		2025-01-25 07:05:20
>> done		2025-01-25 07:05:20
>> checking seqlevels match...		2025-01-25 07:05:20
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> using scanPromoter parameter to scan promoter for each gene...		2025-01-25 07:05:20
>> checking seqlevels match...		2025-01-25 07:05:20
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:05:21
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene...		2025-01-25 07:05:22
>> checking seqlevels match...		2025-01-25 07:05:22
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2025-01-25 07:05:23
>> calculating cor and pvalue, which may be time consuming...		2025-01-25 07:05:23
>> merging all info together...		2025-01-25 07:05:23
>> done		2025-01-25 07:05:23
Joining with `by = join_by(feature_id)`
Joining with `by = join_by(feature_id)`
`geom_smooth()` using formula = 'y ~ x'
Joining with `by = join_by(feature_id)`
Joining with `by = join_by(feature_id)`
`geom_smooth()` using formula = 'y ~ x'
[ FAIL 0 | WARN 0 | SKIP 0 | PASS 65 ]
> 
> proc.time()
   user  system elapsed 
 90.536   2.458  93.181 

Example timings

FindIT2.Rcheck/FindIT2-Ex.timings

nameusersystemelapsed
TF_target_database000
calcRP_TFHit4.7790.2035.142
calcRP_coverage8.5580.1728.745
calcRP_region6.7930.1927.001
enhancerPromoterCor3.5580.1473.712
findIT_MARA0.6180.0400.660
findIT_TFHit1.3910.0591.454
findIT_TTPair0.0940.0000.094
findIT_enrichFisher0.2150.0000.215
findIT_enrichWilcox0.2420.0040.247
findIT_regionRP8.2580.2208.492
getAssocPairNumber1.5500.0241.577
integrate_ChIP_RNA2.8510.0682.925
integrate_replicates0.0030.0000.003
jaccard_findIT_TTpair0.1300.0040.135
jaccard_findIT_enrichFisher0.2600.0000.261
loadPeakFile0.0720.0080.079
mm_geneBound1.6230.0441.670
mm_geneScan2.6730.1472.826
mm_nearestGene1.4620.0041.470
peakGeneCor3.1200.0593.186
plot_annoDistance1.9380.1322.073
plot_peakGeneAlias_summary1.8100.0721.885
plot_peakGeneCor4.0090.0844.101
test_geneSet000