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HostnameOSArch (*)R versionInstalled pkgs
nebbiolo2Linux (Ubuntu 24.04.3 LTS)x86_644.5.2 (2025-10-31) -- "[Not] Part in a Rumble" 4615
merida1macOS 12.7.6 Montereyx86_644.5.2 Patched (2025-11-05 r88990) -- "[Not] Part in a Rumble" 4610
kjohnson1macOS 13.7.5 Venturaarm644.5.2 Patched (2025-11-04 r88984) -- "[Not] Part in a Rumble" 4598
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Package 738/2361HostnameOS / ArchINSTALLBUILDCHECKBUILD BIN
FindIT2 1.16.0  (landing page)
Guandong Shang
Snapshot Date: 2025-11-17 13:45 -0500 (Mon, 17 Nov 2025)
git_url: https://git.bioconductor.org/packages/FindIT2
git_branch: RELEASE_3_22
git_last_commit: 4bef48e
git_last_commit_date: 2025-10-29 11:10:30 -0500 (Wed, 29 Oct 2025)
nebbiolo2Linux (Ubuntu 24.04.3 LTS) / x86_64  OK    OK    OK  UNNEEDED, same version is already published
merida1macOS 12.7.6 Monterey / x86_64  OK    OK    OK    OK  UNNEEDED, same version is already published
kjohnson1macOS 13.7.5 Ventura / arm64  OK    OK    OK    OK  UNNEEDED, same version is already published
taishanLinux (openEuler 24.03 LTS) / aarch64  OK    OK    OK  


CHECK results for FindIT2 on merida1

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.
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raw results


Summary

Package: FindIT2
Version: 1.16.0
Command: /Library/Frameworks/R.framework/Resources/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/Library/Frameworks/R.framework/Resources/library --no-vignettes --timings FindIT2_1.16.0.tar.gz
StartedAt: 2025-11-18 07:36:16 -0500 (Tue, 18 Nov 2025)
EndedAt: 2025-11-18 07:48:59 -0500 (Tue, 18 Nov 2025)
EllapsedTime: 762.2 seconds
RetCode: 0
Status:   OK  
CheckDir: FindIT2.Rcheck
Warnings: 0

Command output

##############################################################################
##############################################################################
###
### Running command:
###
###   /Library/Frameworks/R.framework/Resources/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/Library/Frameworks/R.framework/Resources/library --no-vignettes --timings FindIT2_1.16.0.tar.gz
###
##############################################################################
##############################################################################


* using log directory ‘/Users/biocbuild/bbs-3.22-bioc/meat/FindIT2.Rcheck’
* using R version 4.5.2 Patched (2025-11-05 r88990)
* using platform: x86_64-apple-darwin20
* R was compiled by
    Apple clang version 14.0.0 (clang-1400.0.29.202)
    GNU Fortran (GCC) 14.2.0
* running under: macOS Monterey 12.7.6
* using session charset: UTF-8
* using option ‘--no-vignettes’
* checking for file ‘FindIT2/DESCRIPTION’ ... OK
* this is package ‘FindIT2’ version ‘1.16.0’
* 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 ... 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 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
findIT_regionRP     11.802  0.142  13.443
calcRP_region       10.044  0.203  11.503
plot_peakGeneCor     7.400  0.075   7.851
calcRP_coverage      6.123  0.570   7.407
calcRP_TFHit         6.335  0.287   7.233
enhancerPromoterCor  6.233  0.100   7.056
peakGeneCor          5.331  0.056   5.689
* 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:
###
###   /Library/Frameworks/R.framework/Resources/bin/R CMD INSTALL FindIT2
###
##############################################################################
##############################################################################


* installing to library ‘/Library/Frameworks/R.framework/Versions/4.5-x86_64/Resources/library’
* installing *source* package ‘FindIT2’ ...
** this is package ‘FindIT2’ version ‘1.16.0’
** 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 version 4.5.2 Patched (2025-11-05 r88990) -- "[Not] Part in a Rumble"
Copyright (C) 2025 The R Foundation for Statistical Computing
Platform: x86_64-apple-darwin20

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: Seqinfo
> 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...		2025-11-18 07:46:46
>> some scan range may cross Chr bound, trimming...		2025-11-18 07:46:49
>> preparing weight info...		2025-11-18 07:46:49
>> loading E50h_sampleChr5.bw info...		2025-11-18 07:46:49
------------
>> extracting and calcluating Chr5 signal...		2025-11-18 07:46:50
>> dealing with Chr5 left gene signal...		2025-11-18 07:46:55
>> norming Chr5RP accoring to the whole Chr RP...		2025-11-18 07:46:55
>> merging all Chr RP together...		2025-11-18 07:46:55
>> done		2025-11-18 07:46:55
>> checking seqlevels match...		2025-11-18 07:46:55
>> 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...		2025-11-18 07:46:56
>> some scan range may cross Chr bound, trimming...		2025-11-18 07:46:57
>> finding overlap peak in gene scan region...		2025-11-18 07:46:57
>> dealing with left peak not your gene scan region...		2025-11-18 07:46:57
>> merging two set peaks...		2025-11-18 07:46:58
>> calculating distance and dealing with gene strand...		2025-11-18 07:46:58
>> merging all info together ...		2025-11-18 07:46:58
>> done		2025-11-18 07:46:58
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-18 07:46:58
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2025-11-18 07:47:00
>> calculating RP using centerToTSS and peak score2025-11-18 07:47:00
>> merging all info together		2025-11-18 07:47:04
>> done		2025-11-18 07:47:07
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-18 07:47:07
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2025-11-18 07:47:08
>> calculating RP using centerToTSS and peak score2025-11-18 07:47:08
>> merging all info together		2025-11-18 07:47:15
>> done		2025-11-18 07:47:16
>> checking seqlevels match...		2025-11-18 07:47:16
>> 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...		2025-11-18 07:47:16
>> some scan range may cross Chr bound, trimming...		2025-11-18 07:47:18
>> finding overlap peak in gene scan region...		2025-11-18 07:47:18
>> dealing with left peak not your gene scan region...		2025-11-18 07:47:18
>> merging two set peaks...		2025-11-18 07:47:19
>> calculating distance and dealing with gene strand...		2025-11-18 07:47:19
>> merging all info together ...		2025-11-18 07:47:19
>> done		2025-11-18 07:47:19
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-18 07:47:19
>> calculating RP using centerToTSS and TF hit		2025-11-18 07:47:21
>> merging all info together		2025-11-18 07:47:21
>> done		2025-11-18 07:47:21
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-18 07:47:21
>> calculating RP using centerToTSS and TF hit		2025-11-18 07:47:23
>> merging all info together		2025-11-18 07:47:23
>> done		2025-11-18 07:47:23
>> checking seqlevels match...		2025-11-18 07:47:25
>> 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...		2025-11-18 07:47:25
>> some scan range may cross Chr bound, trimming...		2025-11-18 07:47:27
>> finding overlap peak in gene scan region...		2025-11-18 07:47:27
>> dealing with left peak not your gene scan region...		2025-11-18 07:47:27
>> merging two set peaks...		2025-11-18 07:47:28
>> calculating distance and dealing with gene strand...		2025-11-18 07:47:28
>> merging all info together ...		2025-11-18 07:47:28
>> done		2025-11-18 07:47:28
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-18 07:47:28
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2025-11-18 07:47:29
>> calculating RP using centerToTSS and peak score2025-11-18 07:47:29
>> merging all info together		2025-11-18 07:47:34
>> done		2025-11-18 07:47:35
>> extracting RP info from regionRP...		2025-11-18 07:47:36
>> dealing with TF_GR_databse...		2025-11-18 07:47:36
>> calculating percent and p-value...		2025-11-18 07:47:36
>> dealing withE5_0h_R1...		2025-11-18 07:47:36
>> dealing withE5_0h_R2...		2025-11-18 07:47:36
>> dealing withE5_4h_R1...		2025-11-18 07:47:36
>> dealing withE5_4h_R2...		2025-11-18 07:47:37
>> dealing withE5_8h_R1...		2025-11-18 07:47:37
>> dealing withE5_8h_R2...		2025-11-18 07:47:37
>> dealing withE5_16h_R1...		2025-11-18 07:47:37
>> dealing withE5_16h_R2...		2025-11-18 07:47:37
>> dealing withE5_24h_R1...		2025-11-18 07:47:37
>> dealing withE5_24h_R2...		2025-11-18 07:47:37
>> dealing withE5_48h_R1...		2025-11-18 07:47:37
>> dealing withE5_48h_R2...		2025-11-18 07:47:37
>> dealing withE5_48h_R3...		2025-11-18 07:47:37
>> dealing withE5_72h_R1...		2025-11-18 07:47:38
>> dealing withE5_72h_R2...		2025-11-18 07:47:38
>> dealing withE5_72h_R3...		2025-11-18 07:47:38
>> merging all info together...		2025-11-18 07:47:38
>> done		2025-11-18 07:47:38
>> preparing gene features information...		2025-11-18 07:47:38
>> some scan range may cross Chr bound, trimming...		2025-11-18 07:47:40
>> calculating p-value for each TF, which may be time consuming...		2025-11-18 07:47:40
>> merging all info together...		2025-11-18 07:47:40
>> done		2025-11-18 07:47:40
>> dealing with TF_GR_database...		2025-11-18 07:47:41
>> calculating coef and converting into z-score using INT...		2025-11-18 07:47:41
>> dealing with E5_0h_R1...		2025-11-18 07:47:41
>> dealing with E5_0h_R2...		2025-11-18 07:47:41
>> dealing with E5_4h_R1...		2025-11-18 07:47:41
>> dealing with E5_4h_R2...		2025-11-18 07:47:42
>> dealing with E5_8h_R1...		2025-11-18 07:47:42
>> dealing with E5_8h_R2...		2025-11-18 07:47:42
>> dealing with E5_16h_R1...		2025-11-18 07:47:42
>> dealing with E5_16h_R2...		2025-11-18 07:47:42
>> dealing with E5_24h_R1...		2025-11-18 07:47:43
>> dealing with E5_24h_R2...		2025-11-18 07:47:43
>> dealing with E5_48h_R1...		2025-11-18 07:47:43
>> dealing with E5_48h_R2...		2025-11-18 07:47:43
>> dealing with E5_48h_R3...		2025-11-18 07:47:43
>> dealing with E5_72h_R1...		2025-11-18 07:47:44
>> dealing with E5_72h_R2...		2025-11-18 07:47:44
>> dealing with E5_72h_R3...		2025-11-18 07:47:44
>> merging all info together...		2025-11-18 07:47:44
>> done		2025-11-18 07:47:45
>> checking seqlevels match...		2025-11-18 07:47:45
>> 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...		2025-11-18 07:47:45
>> some scan range may cross Chr bound, trimming...		2025-11-18 07:47:47
>> finding overlap peak in gene scan region...		2025-11-18 07:47:47
>> dealing with left peak not your gene scan region...		2025-11-18 07:47:47
>> merging two set peaks...		2025-11-18 07:47:47
>> calculating distance and dealing with gene strand...		2025-11-18 07:47:47
>> merging all info together ...		2025-11-18 07:47:47
>> done		2025-11-18 07:47:47
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-18 07:47:47
>> calculating RP using centerToTSS and TF hit		2025-11-18 07:47:49
>> merging all info together		2025-11-18 07:47:49
>> done		2025-11-18 07:47:49
>> checking seqlevels match...		2025-11-18 07:47:50
>> your peak_GR seqlevel:5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match...		2025-11-18 07:47:50
>> your peak_GR seqlevel:Chr5 Chr6...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match...		2025-11-18 07:47:56
>> 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...		2025-11-18 07:47:57
>> 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...		2025-11-18 07:47:57
>> finding nearest gene and calculating distance...		2025-11-18 07:47:58
>> dealing with gene strand ...		2025-11-18 07:47:58
>> merging all info together ...		2025-11-18 07:47:58
>> done		2025-11-18 07:47:58
>> checking seqlevels match...		2025-11-18 07:47:59
>> 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...		2025-11-18 07:47:59
>> 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...		2025-11-18 07:47:59
>> finding nearest gene and calculating distance...		2025-11-18 07:48:00
>> dealing with gene strand ...		2025-11-18 07:48:01
>> merging all info together ...		2025-11-18 07:48:01
>> done		2025-11-18 07:48:01
>> checking seqlevels match...		2025-11-18 07:48:03
>> 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...		2025-11-18 07:48:04
>> 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...		2025-11-18 07:48:04
>> finding nearest gene and calculating distance...		2025-11-18 07:48:06
>> dealing with gene strand ...		2025-11-18 07:48:07
>> merging all info together ...		2025-11-18 07:48:07
>> done		2025-11-18 07:48:07
>> checking seqlevels match...		2025-11-18 07:48:08
>> 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
>> checking seqlevels match...		2025-11-18 07:48:08
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2025-11-18 07:48:09
>> finding nearest gene and calculating distance...		2025-11-18 07:48:10
>> dealing with gene strand ...		2025-11-18 07:48:10
>> merging all info together ...		2025-11-18 07:48:10
>> done		2025-11-18 07:48:10
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match...		2025-11-18 07:48:12
>> 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...		2025-11-18 07:48:12
>> 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...		2025-11-18 07:48:12
>> finding nearest gene and calculating distance...		2025-11-18 07:48:14
>> dealing with gene strand ...		2025-11-18 07:48:14
>> merging all info together ...		2025-11-18 07:48:14
>> done		2025-11-18 07:48:14
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match...		2025-11-18 07:48:16
>> 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...		2025-11-18 07:48:18
>> 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
>> some scan range may cross Chr bound, trimming...		2025-11-18 07:48:19
>> checking seqlevels match...		2025-11-18 07:48:21
>> 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...		2025-11-18 07:48:23
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2025-11-18 07:48:26
>> merging all info together...		2025-11-18 07:48:26
>> done		2025-11-18 07:48:26
>> checking seqlevels match...		2025-11-18 07:48:27
>> 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...		2025-11-18 07:48:27
>> checking seqlevels match...		2025-11-18 07:48:27
>> 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...		2025-11-18 07:48:28
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene...		2025-11-18 07:48:29
>> checking seqlevels match...		2025-11-18 07:48:29
>> 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...		2025-11-18 07:48:30
>> calculating cor and pvalue, which may be time consuming...		2025-11-18 07:48:31
>> merging all info together...		2025-11-18 07:48:31
>> done		2025-11-18 07:48:31
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2025-11-18 07:48:31
>> merging all info together...		2025-11-18 07:48:32
>> done		2025-11-18 07:48:32
>> checking seqlevels match...		2025-11-18 07:48:32
>> 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...		2025-11-18 07:48:32
>> some scan range may cross Chr bound, trimming...		2025-11-18 07:48:34
>> finding overlap peak in gene scan region...		2025-11-18 07:48:34
>> dealing with left peak not your gene scan region...		2025-11-18 07:48:34
>> merging two set peaks...		2025-11-18 07:48:34
>> calculating distance and dealing with gene strand...		2025-11-18 07:48:34
>> merging all info together ...		2025-11-18 07:48:34
>> done		2025-11-18 07:48:34
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2025-11-18 07:48:37
>> merging all info together...		2025-11-18 07:48:37
>> done		2025-11-18 07:48:38
>> checking seqlevels match...		2025-11-18 07:48:38
>> 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...		2025-11-18 07:48:38
>> checking seqlevels match...		2025-11-18 07:48:38
>> 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...		2025-11-18 07:48:39
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene...		2025-11-18 07:48:40
>> checking seqlevels match...		2025-11-18 07:48:40
>> 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...		2025-11-18 07:48:42
>> calculating cor and pvalue, which may be time consuming...		2025-11-18 07:48:42
>> merging all info together...		2025-11-18 07:48:42
>> done		2025-11-18 07:48:43
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 
131.727   3.572 145.309 

Example timings

FindIT2.Rcheck/FindIT2-Ex.timings

nameusersystemelapsed
TF_target_database0.0010.0010.001
calcRP_TFHit6.3350.2877.233
calcRP_coverage6.1230.5707.407
calcRP_region10.044 0.20311.503
enhancerPromoterCor6.2330.1007.056
findIT_MARA0.9620.0331.149
findIT_TFHit1.7830.0322.155
findIT_TTPair0.1520.0080.179
findIT_enrichFisher0.3380.0070.399
findIT_enrichWilcox0.3710.0080.433
findIT_regionRP11.802 0.14213.443
getAssocPairNumber2.3040.0412.404
integrate_ChIP_RNA4.0150.0764.561
integrate_replicates0.0050.0020.008
jaccard_findIT_TTpair0.2520.0220.289
jaccard_findIT_enrichFisher0.4380.0090.465
loadPeakFile0.1290.0030.138
mm_geneBound2.3300.0312.504
mm_geneScan2.4270.0392.602
mm_nearestGene2.1570.0402.307
peakGeneCor5.3310.0565.689
plot_annoDistance3.5650.0553.850
plot_peakGeneAlias_summary2.7700.0362.953
plot_peakGeneCor7.4000.0757.851
test_geneSet0.0000.0020.002