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This page was generated on 2025-12-01 11:35 -0500 (Mon, 01 Dec 2025).

HostnameOSArch (*)R versionInstalled pkgs
nebbiolo1Linux (Ubuntu 24.04.3 LTS)x86_64R Under development (unstable) (2025-10-20 r88955) -- "Unsuffered Consequences" 4866
kjohnson3macOS 13.7.7 Venturaarm64R Under development (unstable) (2025-11-04 r88984) -- "Unsuffered Consequences" 4572
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Package 730/2328HostnameOS / ArchINSTALLBUILDCHECKBUILD BIN
FindIT2 1.17.0  (landing page)
Guandong Shang
Snapshot Date: 2025-11-30 13:40 -0500 (Sun, 30 Nov 2025)
git_url: https://git.bioconductor.org/packages/FindIT2
git_branch: devel
git_last_commit: 6e3f32a
git_last_commit_date: 2025-10-29 11:10:30 -0500 (Wed, 29 Oct 2025)
nebbiolo1Linux (Ubuntu 24.04.3 LTS) / x86_64  OK    OK    OK  UNNEEDED, same version is already published
kjohnson3macOS 13.7.7 Ventura / arm64  OK    OK    OK    OK  NO, package depends on 'GenomicRanges' which is only available as a source package that needs compilation


CHECK results for FindIT2 on nebbiolo1

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.

raw results


Summary

Package: FindIT2
Version: 1.17.0
Command: /home/biocbuild/bbs-3.23-bioc/R/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/home/biocbuild/bbs-3.23-bioc/R/site-library --timings FindIT2_1.17.0.tar.gz
StartedAt: 2025-11-30 23:41:04 -0500 (Sun, 30 Nov 2025)
EndedAt: 2025-11-30 23:47:49 -0500 (Sun, 30 Nov 2025)
EllapsedTime: 404.7 seconds
RetCode: 0
Status:   OK  
CheckDir: FindIT2.Rcheck
Warnings: 0

Command output

##############################################################################
##############################################################################
###
### Running command:
###
###   /home/biocbuild/bbs-3.23-bioc/R/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/home/biocbuild/bbs-3.23-bioc/R/site-library --timings FindIT2_1.17.0.tar.gz
###
##############################################################################
##############################################################################


* using log directory ‘/home/biocbuild/bbs-3.23-bioc/meat/FindIT2.Rcheck’
* using R Under development (unstable) (2025-10-20 r88955)
* using platform: x86_64-pc-linux-gnu
* R was compiled by
    gcc (Ubuntu 13.3.0-6ubuntu2~24.04) 13.3.0
    GNU Fortran (Ubuntu 13.3.0-6ubuntu2~24.04) 13.3.0
* running under: Ubuntu 24.04.3 LTS
* using session charset: UTF-8
* checking for file ‘FindIT2/DESCRIPTION’ ... OK
* this is package ‘FindIT2’ version ‘1.17.0’
* 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 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
findIT_regionRP 6.147  0.121   6.268
calcRP_region   5.214  0.067   5.282
* 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 re-building of vignette outputs ... OK
* checking PDF version of manual ... OK
* DONE

Status: OK


Installation output

FindIT2.Rcheck/00install.out

##############################################################################
##############################################################################
###
### Running command:
###
###   /home/biocbuild/bbs-3.23-bioc/R/bin/R CMD INSTALL FindIT2
###
##############################################################################
##############################################################################


* installing to library ‘/home/biocbuild/bbs-3.23-bioc/R/site-library’
* installing *source* package ‘FindIT2’ ...
** this is package ‘FindIT2’ version ‘1.17.0’
** 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 Under development (unstable) (2025-10-20 r88955) -- "Unsuffered Consequences"
Copyright (C) 2025 The R Foundation for Statistical Computing
Platform: x86_64-pc-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: 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...		2025-11-30 23:45:54
>> some scan range may cross Chr bound, trimming...		2025-11-30 23:45:56
>> preparing weight info...		2025-11-30 23:45:56
>> loading E50h_sampleChr5.bw info...		2025-11-30 23:45:56
------------
>> extracting and calcluating Chr5 signal...		2025-11-30 23:45:56
>> dealing with Chr5 left gene signal...		2025-11-30 23:45:59
>> norming Chr5RP accoring to the whole Chr RP...		2025-11-30 23:45:59
>> merging all Chr RP together...		2025-11-30 23:45:59
>> done		2025-11-30 23:45:59
>> checking seqlevels match...		2025-11-30 23:45:59
>> 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
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2025-11-30 23:45:59
>> some scan range may cross Chr bound, trimming...		2025-11-30 23:46:00
>> finding overlap peak in gene scan region...		2025-11-30 23:46:00
>> dealing with left peak not your gene scan region...		2025-11-30 23:46:00
>> merging two set peaks...		2025-11-30 23:46:00
>> calculating distance and dealing with gene strand...		2025-11-30 23:46:00
>> merging all info together ...		2025-11-30 23:46:00
>> done		2025-11-30 23:46:00
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-30 23:46:00
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2025-11-30 23:46:01
>> calculating RP using centerToTSS and peak score2025-11-30 23:46:01
>> merging all info together		2025-11-30 23:46:03
>> done		2025-11-30 23:46:04
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-30 23:46:04
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2025-11-30 23:46:05
>> calculating RP using centerToTSS and peak score2025-11-30 23:46:05
>> merging all info together		2025-11-30 23:46:07
>> done		2025-11-30 23:46:07
>> checking seqlevels match...		2025-11-30 23:46:07
>> 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
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2025-11-30 23:46:08
>> some scan range may cross Chr bound, trimming...		2025-11-30 23:46:08
>> finding overlap peak in gene scan region...		2025-11-30 23:46:08
>> dealing with left peak not your gene scan region...		2025-11-30 23:46:08
>> merging two set peaks...		2025-11-30 23:46:08
>> calculating distance and dealing with gene strand...		2025-11-30 23:46:08
>> merging all info together ...		2025-11-30 23:46:09
>> done		2025-11-30 23:46:09
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-30 23:46:09
>> calculating RP using centerToTSS and TF hit		2025-11-30 23:46:09
>> merging all info together		2025-11-30 23:46:09
>> done		2025-11-30 23:46:09
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-30 23:46:09
>> calculating RP using centerToTSS and TF hit		2025-11-30 23:46:10
>> merging all info together		2025-11-30 23:46:10
>> done		2025-11-30 23:46:10
>> checking seqlevels match...		2025-11-30 23:46:11
>> 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...		2025-11-30 23:46:11
>> some scan range may cross Chr bound, trimming...		2025-11-30 23:46:11
>> finding overlap peak in gene scan region...		2025-11-30 23:46:11
>> dealing with left peak not your gene scan region...		2025-11-30 23:46:11
>> merging two set peaks...		2025-11-30 23:46:13
>> calculating distance and dealing with gene strand...		2025-11-30 23:46:13
>> merging all info together ...		2025-11-30 23:46:13
>> done		2025-11-30 23:46:13
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-30 23:46:13
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2025-11-30 23:46:13
>> calculating RP using centerToTSS and peak score2025-11-30 23:46:13
>> merging all info together		2025-11-30 23:46:15
>> done		2025-11-30 23:46:15
>> extracting RP info from regionRP...		2025-11-30 23:46:16
>> dealing with TF_GR_databse...		2025-11-30 23:46:16
>> calculating percent and p-value...		2025-11-30 23:46:16
>> dealing withE5_0h_R1...		2025-11-30 23:46:16
>> dealing withE5_0h_R2...		2025-11-30 23:46:16
>> dealing withE5_4h_R1...		2025-11-30 23:46:16
>> dealing withE5_4h_R2...		2025-11-30 23:46:16
>> dealing withE5_8h_R1...		2025-11-30 23:46:16
>> dealing withE5_8h_R2...		2025-11-30 23:46:16
>> dealing withE5_16h_R1...		2025-11-30 23:46:16
>> dealing withE5_16h_R2...		2025-11-30 23:46:16
>> dealing withE5_24h_R1...		2025-11-30 23:46:16
>> dealing withE5_24h_R2...		2025-11-30 23:46:16
>> dealing withE5_48h_R1...		2025-11-30 23:46:17
>> dealing withE5_48h_R2...		2025-11-30 23:46:17
>> dealing withE5_48h_R3...		2025-11-30 23:46:17
>> dealing withE5_72h_R1...		2025-11-30 23:46:17
>> dealing withE5_72h_R2...		2025-11-30 23:46:17
>> dealing withE5_72h_R3...		2025-11-30 23:46:17
>> merging all info together...		2025-11-30 23:46:17
>> done		2025-11-30 23:46:17
>> preparing gene features information...		2025-11-30 23:46:17
>> some scan range may cross Chr bound, trimming...		2025-11-30 23:46:18
>> calculating p-value for each TF, which may be time consuming...		2025-11-30 23:46:18
>> merging all info together...		2025-11-30 23:46:18
>> done		2025-11-30 23:46:18
>> dealing with TF_GR_database...		2025-11-30 23:46:18
>> calculating coef and converting into z-score using INT...		2025-11-30 23:46:18
>> dealing with E5_0h_R1...		2025-11-30 23:46:18
>> dealing with E5_0h_R2...		2025-11-30 23:46:18
>> dealing with E5_4h_R1...		2025-11-30 23:46:18
>> dealing with E5_4h_R2...		2025-11-30 23:46:18
>> dealing with E5_8h_R1...		2025-11-30 23:46:18
>> dealing with E5_8h_R2...		2025-11-30 23:46:18
>> dealing with E5_16h_R1...		2025-11-30 23:46:18
>> dealing with E5_16h_R2...		2025-11-30 23:46:18
>> dealing with E5_24h_R1...		2025-11-30 23:46:19
>> dealing with E5_24h_R2...		2025-11-30 23:46:19
>> dealing with E5_48h_R1...		2025-11-30 23:46:19
>> dealing with E5_48h_R2...		2025-11-30 23:46:19
>> dealing with E5_48h_R3...		2025-11-30 23:46:19
>> dealing with E5_72h_R1...		2025-11-30 23:46:19
>> dealing with E5_72h_R2...		2025-11-30 23:46:19
>> dealing with E5_72h_R3...		2025-11-30 23:46:19
>> merging all info together...		2025-11-30 23:46:19
>> done		2025-11-30 23:46:19
>> checking seqlevels match...		2025-11-30 23:46:19
>> 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...		2025-11-30 23:46:19
>> some scan range may cross Chr bound, trimming...		2025-11-30 23:46:20
>> finding overlap peak in gene scan region...		2025-11-30 23:46:20
>> dealing with left peak not your gene scan region...		2025-11-30 23:46:20
>> merging two set peaks...		2025-11-30 23:46:20
>> calculating distance and dealing with gene strand...		2025-11-30 23:46:20
>> merging all info together ...		2025-11-30 23:46:20
>> done		2025-11-30 23:46:20
>> calculating peakCenter to TSS using peak-gene pair...		2025-11-30 23:46:20
>> calculating RP using centerToTSS and TF hit		2025-11-30 23:46:21
>> merging all info together		2025-11-30 23:46:21
>> done		2025-11-30 23:46:21
>> checking seqlevels match...		2025-11-30 23:46:21
>> your peak_GR seqlevel:5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match...		2025-11-30 23:46:21
>> your peak_GR seqlevel:Chr5 Chr6...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match...		2025-11-30 23:46:24
>> 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...		2025-11-30 23:46:24
>> 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...		2025-11-30 23:46:24
>> finding nearest gene and calculating distance...		2025-11-30 23:46:25
>> dealing with gene strand ...		2025-11-30 23:46:25
>> merging all info together ...		2025-11-30 23:46:25
>> done		2025-11-30 23:46:25
>> checking seqlevels match...		2025-11-30 23:46:25
>> 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
>> checking seqlevels match...		2025-11-30 23:46:25
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2025-11-30 23:46:25
>> finding nearest gene and calculating distance...		2025-11-30 23:46:26
>> dealing with gene strand ...		2025-11-30 23:46:26
>> merging all info together ...		2025-11-30 23:46:26
>> done		2025-11-30 23:46:26
>> checking seqlevels match...		2025-11-30 23:46:27
>> 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
>> checking seqlevels match...		2025-11-30 23:46:27
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2025-11-30 23:46:27
>> finding nearest gene and calculating distance...		2025-11-30 23:46:28
>> dealing with gene strand ...		2025-11-30 23:46:28
>> merging all info together ...		2025-11-30 23:46:28
>> done		2025-11-30 23:46:28
>> checking seqlevels match...		2025-11-30 23:46:29
>> 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
>> checking seqlevels match...		2025-11-30 23:46:29
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2025-11-30 23:46:29
>> finding nearest gene and calculating distance...		2025-11-30 23:46:29
>> dealing with gene strand ...		2025-11-30 23:46:30
>> merging all info together ...		2025-11-30 23:46:30
>> done		2025-11-30 23:46:30
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match...		2025-11-30 23:46:30
>> 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...		2025-11-30 23:46:30
>> 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...		2025-11-30 23:46:30
>> finding nearest gene and calculating distance...		2025-11-30 23:46:31
>> dealing with gene strand ...		2025-11-30 23:46:31
>> merging all info together ...		2025-11-30 23:46:31
>> done		2025-11-30 23:46:31
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match...		2025-11-30 23:46:32
>> 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
>> checking seqlevels match...		2025-11-30 23:46:33
>> 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...		2025-11-30 23:46:33
>> checking seqlevels match...		2025-11-30 23:46:34
>> 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...		2025-11-30 23:46:35
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2025-11-30 23:46:36
>> merging all info together...		2025-11-30 23:46:36
>> done		2025-11-30 23:46:36
>> checking seqlevels match...		2025-11-30 23:46:36
>> 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
>> using scanPromoter parameter to scan promoter for each gene...		2025-11-30 23:46:36
>> checking seqlevels match...		2025-11-30 23:46:36
>> 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
>> some scan range may cross Chr bound, trimming...		2025-11-30 23:46:37
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene...		2025-11-30 23:46:37
>> checking seqlevels match...		2025-11-30 23:46:37
>> 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...		2025-11-30 23:46:38
>> calculating cor and pvalue, which may be time consuming...		2025-11-30 23:46:39
>> merging all info together...		2025-11-30 23:46:39
>> done		2025-11-30 23:46:39
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2025-11-30 23:46:39
>> merging all info together...		2025-11-30 23:46:39
>> done		2025-11-30 23:46:39
>> checking seqlevels match...		2025-11-30 23:46:39
>> 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...		2025-11-30 23:46:39
>> some scan range may cross Chr bound, trimming...		2025-11-30 23:46:40
>> finding overlap peak in gene scan region...		2025-11-30 23:46:40
>> dealing with left peak not your gene scan region...		2025-11-30 23:46:40
>> merging two set peaks...		2025-11-30 23:46:40
>> calculating distance and dealing with gene strand...		2025-11-30 23:46:40
>> merging all info together ...		2025-11-30 23:46:40
>> done		2025-11-30 23:46:40
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2025-11-30 23:46:41
>> merging all info together...		2025-11-30 23:46:41
>> done		2025-11-30 23:46:41
>> checking seqlevels match...		2025-11-30 23:46:41
>> 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...		2025-11-30 23:46:41
>> checking seqlevels match...		2025-11-30 23:46:41
>> 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...		2025-11-30 23:46:42
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene...		2025-11-30 23:46:42
>> checking seqlevels match...		2025-11-30 23:46:42
>> 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...		2025-11-30 23:46:43
>> calculating cor and pvalue, which may be time consuming...		2025-11-30 23:46:43
>> merging all info together...		2025-11-30 23:46:43
>> done		2025-11-30 23:46:43
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 
 59.558   2.034  61.592 

Example timings

FindIT2.Rcheck/FindIT2-Ex.timings

nameusersystemelapsed
TF_target_database0.0010.0000.001
calcRP_TFHit3.1900.1723.380
calcRP_coverage2.6010.2322.834
calcRP_region5.2140.0675.282
enhancerPromoterCor2.2620.0422.305
findIT_MARA0.4190.0060.425
findIT_TFHit0.8060.0500.856
findIT_TTPair0.0690.0020.071
findIT_enrichFisher0.1420.0020.144
findIT_enrichWilcox0.1590.0000.159
findIT_regionRP6.1470.1216.268
getAssocPairNumber0.9930.0101.003
integrate_ChIP_RNA1.8050.0111.816
integrate_replicates0.0010.0010.003
jaccard_findIT_TTpair0.0960.0020.098
jaccard_findIT_enrichFisher0.1860.0150.201
loadPeakFile0.0560.0030.059
mm_geneBound1.0640.0651.129
mm_geneScan1.0500.0081.058
mm_nearestGene1.8200.0351.855
peakGeneCor2.0140.0752.089
plot_annoDistance1.4390.0331.471
plot_peakGeneAlias_summary1.1700.0051.175
plot_peakGeneCor2.7480.0412.790
test_geneSet0.0010.0000.001