Guandong Shang
| Snapshot Date: 2025-10-30 13:45 -0400 (Thu, 30 Oct 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 -0400 (Wed, 29 Oct 2025) |
| Back to Multiple platform build/check report for BioC 3.22: simplified long |
|
This page was generated on 2025-10-31 12:04 -0400 (Fri, 31 Oct 2025).
| Hostname | OS | Arch (*) | R version | Installed pkgs |
|---|---|---|---|---|
| nebbiolo2 | Linux (Ubuntu 24.04.3 LTS) | x86_64 | 4.5.1 Patched (2025-08-23 r88802) -- "Great Square Root" | 4901 |
| lconway | macOS 12.7.6 Monterey | x86_64 | 4.5.1 Patched (2025-09-10 r88807) -- "Great Square Root" | 4691 |
| kjohnson3 | macOS 13.7.7 Ventura | arm64 | 4.5.1 Patched (2025-09-10 r88807) -- "Great Square Root" | 4637 |
| 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 738/2361 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||||
| FindIT2 1.16.0 (landing page) Guandong Shang
| nebbiolo2 | Linux (Ubuntu 24.04.3 LTS) / x86_64 | OK | OK | OK | | ||||||||
| lconway | macOS 12.7.6 Monterey / x86_64 | OK | OK | OK | OK | | ||||||||
| kjohnson3 | macOS 13.7.7 Ventura / arm64 | OK | OK | OK | OK | | ||||||||
|
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. |
| 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: 2025-10-30 21:04:18 -0400 (Thu, 30 Oct 2025) |
| EndedAt: 2025-10-30 21:10:48 -0400 (Thu, 30 Oct 2025) |
| EllapsedTime: 390.1 seconds |
| RetCode: 0 |
| Status: OK |
| CheckDir: FindIT2.Rcheck |
| Warnings: 0 |
##############################################################################
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###
### 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 4.5.1 Patched (2025-09-10 r88807)
* 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 6.515 0.148 6.686
calcRP_region 4.935 0.198 5.147
* 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
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)
FindIT2.Rcheck/tests/testthat.Rout
R version 4.5.1 Patched (2025-09-10 r88807) -- "Great Square Root"
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... 2025-10-30 21:09:38
>> some scan range may cross Chr bound, trimming... 2025-10-30 21:09:40
>> preparing weight info... 2025-10-30 21:09:40
>> loading E50h_sampleChr5.bw info... 2025-10-30 21:09:40
------------
>> extracting and calcluating Chr5 signal... 2025-10-30 21:09:40
>> dealing with Chr5 left gene signal... 2025-10-30 21:09:44
>> norming Chr5RP accoring to the whole Chr RP... 2025-10-30 21:09:44
>> merging all Chr RP together... 2025-10-30 21:09:44
>> done 2025-10-30 21:09:44
>> checking seqlevels match... 2025-10-30 21:09:44
>> 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... 2025-10-30 21:09:44
>> some scan range may cross Chr bound, trimming... 2025-10-30 21:09:45
>> finding overlap peak in gene scan region... 2025-10-30 21:09:45
>> dealing with left peak not your gene scan region... 2025-10-30 21:09:45
>> merging two set peaks... 2025-10-30 21:09:46
>> calculating distance and dealing with gene strand... 2025-10-30 21:09:46
>> merging all info together ... 2025-10-30 21:09:46
>> done 2025-10-30 21:09:46
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-30 21:09:46
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2025-10-30 21:09:47
>> calculating RP using centerToTSS and peak score2025-10-30 21:09:47
>> merging all info together 2025-10-30 21:09:49
>> done 2025-10-30 21:09:50
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-30 21:09:50
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2025-10-30 21:09:51
>> calculating RP using centerToTSS and peak score2025-10-30 21:09:51
>> merging all info together 2025-10-30 21:09:54
>> done 2025-10-30 21:09:54
>> checking seqlevels match... 2025-10-30 21:09:55
>> 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... 2025-10-30 21:09:55
>> some scan range may cross Chr bound, trimming... 2025-10-30 21:09:56
>> finding overlap peak in gene scan region... 2025-10-30 21:09:56
>> dealing with left peak not your gene scan region... 2025-10-30 21:09:56
>> merging two set peaks... 2025-10-30 21:09:56
>> calculating distance and dealing with gene strand... 2025-10-30 21:09:56
>> merging all info together ... 2025-10-30 21:09:56
>> done 2025-10-30 21:09:56
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-30 21:09:56
>> calculating RP using centerToTSS and TF hit 2025-10-30 21:09:57
>> merging all info together 2025-10-30 21:09:57
>> done 2025-10-30 21:09:57
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-30 21:09:57
>> calculating RP using centerToTSS and TF hit 2025-10-30 21:09:58
>> merging all info together 2025-10-30 21:09:58
>> done 2025-10-30 21:09:58
>> checking seqlevels match... 2025-10-30 21:09:59
>> 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... 2025-10-30 21:09:59
>> some scan range may cross Chr bound, trimming... 2025-10-30 21:10:00
>> finding overlap peak in gene scan region... 2025-10-30 21:10:00
>> dealing with left peak not your gene scan region... 2025-10-30 21:10:00
>> merging two set peaks... 2025-10-30 21:10:01
>> calculating distance and dealing with gene strand... 2025-10-30 21:10:01
>> merging all info together ... 2025-10-30 21:10:01
>> done 2025-10-30 21:10:01
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-30 21:10:01
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2025-10-30 21:10:02
>> calculating RP using centerToTSS and peak score2025-10-30 21:10:02
>> merging all info together 2025-10-30 21:10:04
>> done 2025-10-30 21:10:04
>> extracting RP info from regionRP... 2025-10-30 21:10:05
>> dealing with TF_GR_databse... 2025-10-30 21:10:05
>> calculating percent and p-value... 2025-10-30 21:10:05
>> dealing withE5_0h_R1... 2025-10-30 21:10:05
>> dealing withE5_0h_R2... 2025-10-30 21:10:05
>> dealing withE5_4h_R1... 2025-10-30 21:10:05
>> dealing withE5_4h_R2... 2025-10-30 21:10:05
>> dealing withE5_8h_R1... 2025-10-30 21:10:05
>> dealing withE5_8h_R2... 2025-10-30 21:10:05
>> dealing withE5_16h_R1... 2025-10-30 21:10:05
>> dealing withE5_16h_R2... 2025-10-30 21:10:05
>> dealing withE5_24h_R1... 2025-10-30 21:10:06
>> dealing withE5_24h_R2... 2025-10-30 21:10:06
>> dealing withE5_48h_R1... 2025-10-30 21:10:06
>> dealing withE5_48h_R2... 2025-10-30 21:10:06
>> dealing withE5_48h_R3... 2025-10-30 21:10:06
>> dealing withE5_72h_R1... 2025-10-30 21:10:06
>> dealing withE5_72h_R2... 2025-10-30 21:10:06
>> dealing withE5_72h_R3... 2025-10-30 21:10:06
>> merging all info together... 2025-10-30 21:10:06
>> done 2025-10-30 21:10:06
>> preparing gene features information... 2025-10-30 21:10:06
>> some scan range may cross Chr bound, trimming... 2025-10-30 21:10:07
>> calculating p-value for each TF, which may be time consuming... 2025-10-30 21:10:07
>> merging all info together... 2025-10-30 21:10:07
>> done 2025-10-30 21:10:07
>> dealing with TF_GR_database... 2025-10-30 21:10:07
>> calculating coef and converting into z-score using INT... 2025-10-30 21:10:07
>> dealing with E5_0h_R1... 2025-10-30 21:10:07
>> dealing with E5_0h_R2... 2025-10-30 21:10:08
>> dealing with E5_4h_R1... 2025-10-30 21:10:08
>> dealing with E5_4h_R2... 2025-10-30 21:10:08
>> dealing with E5_8h_R1... 2025-10-30 21:10:08
>> dealing with E5_8h_R2... 2025-10-30 21:10:08
>> dealing with E5_16h_R1... 2025-10-30 21:10:08
>> dealing with E5_16h_R2... 2025-10-30 21:10:08
>> dealing with E5_24h_R1... 2025-10-30 21:10:08
>> dealing with E5_24h_R2... 2025-10-30 21:10:08
>> dealing with E5_48h_R1... 2025-10-30 21:10:08
>> dealing with E5_48h_R2... 2025-10-30 21:10:08
>> dealing with E5_48h_R3... 2025-10-30 21:10:08
>> dealing with E5_72h_R1... 2025-10-30 21:10:08
>> dealing with E5_72h_R2... 2025-10-30 21:10:08
>> dealing with E5_72h_R3... 2025-10-30 21:10:09
>> merging all info together... 2025-10-30 21:10:09
>> done 2025-10-30 21:10:09
>> checking seqlevels match... 2025-10-30 21:10:09
>> 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... 2025-10-30 21:10:09
>> some scan range may cross Chr bound, trimming... 2025-10-30 21:10:10
>> finding overlap peak in gene scan region... 2025-10-30 21:10:10
>> dealing with left peak not your gene scan region... 2025-10-30 21:10:10
>> merging two set peaks... 2025-10-30 21:10:10
>> calculating distance and dealing with gene strand... 2025-10-30 21:10:10
>> merging all info together ... 2025-10-30 21:10:10
>> done 2025-10-30 21:10:10
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-30 21:10:10
>> calculating RP using centerToTSS and TF hit 2025-10-30 21:10:11
>> merging all info together 2025-10-30 21:10:11
>> done 2025-10-30 21:10:11
>> checking seqlevels match... 2025-10-30 21:10:11
>> your peak_GR seqlevel:5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match... 2025-10-30 21:10:11
>> your peak_GR seqlevel:Chr5 Chr6...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match... 2025-10-30 21:10:15
>> 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
>> checking seqlevels match... 2025-10-30 21:10:15
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2025-10-30 21:10:15
>> finding nearest gene and calculating distance... 2025-10-30 21:10:15
>> dealing with gene strand ... 2025-10-30 21:10:16
>> merging all info together ... 2025-10-30 21:10:16
>> done 2025-10-30 21:10:16
>> checking seqlevels match... 2025-10-30 21:10:16
>> 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... 2025-10-30 21:10:16
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2025-10-30 21:10:16
>> finding nearest gene and calculating distance... 2025-10-30 21:10:17
>> dealing with gene strand ... 2025-10-30 21:10:17
>> merging all info together ... 2025-10-30 21:10:17
>> done 2025-10-30 21:10:17
>> checking seqlevels match... 2025-10-30 21:10:18
>> 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
>> checking seqlevels match... 2025-10-30 21:10:18
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2025-10-30 21:10:18
>> finding nearest gene and calculating distance... 2025-10-30 21:10:19
>> dealing with gene strand ... 2025-10-30 21:10:19
>> merging all info together ... 2025-10-30 21:10:19
>> done 2025-10-30 21:10:19
>> checking seqlevels match... 2025-10-30 21:10:20
>> 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
>> checking seqlevels match... 2025-10-30 21:10:20
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2025-10-30 21:10:20
>> finding nearest gene and calculating distance... 2025-10-30 21:10:21
>> dealing with gene strand ... 2025-10-30 21:10:21
>> merging all info together ... 2025-10-30 21:10:21
>> done 2025-10-30 21:10:21
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match... 2025-10-30 21:10:22
>> 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
>> checking seqlevels match... 2025-10-30 21:10:22
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2025-10-30 21:10:22
>> finding nearest gene and calculating distance... 2025-10-30 21:10:23
>> dealing with gene strand ... 2025-10-30 21:10:23
>> merging all info together ... 2025-10-30 21:10:23
>> done 2025-10-30 21:10:23
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match... 2025-10-30 21:10:24
>> 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... 2025-10-30 21:10:25
>> 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
>> some scan range may cross Chr bound, trimming... 2025-10-30 21:10:26
>> checking seqlevels match... 2025-10-30 21:10:26
>> 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... 2025-10-30 21:10:27
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2025-10-30 21:10:28
>> merging all info together... 2025-10-30 21:10:29
>> done 2025-10-30 21:10:29
>> checking seqlevels match... 2025-10-30 21:10:29
>> 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
>> using scanPromoter parameter to scan promoter for each gene... 2025-10-30 21:10:29
>> checking seqlevels match... 2025-10-30 21:10:29
>> 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... 2025-10-30 21:10:30
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene... 2025-10-30 21:10:30
>> checking seqlevels match... 2025-10-30 21:10:30
>> 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
>> some scan range may cross Chr bound, trimming... 2025-10-30 21:10:31
>> calculating cor and pvalue, which may be time consuming... 2025-10-30 21:10:31
>> merging all info together... 2025-10-30 21:10:31
>> done 2025-10-30 21:10:31
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2025-10-30 21:10:31
>> merging all info together... 2025-10-30 21:10:31
>> done 2025-10-30 21:10:31
>> checking seqlevels match... 2025-10-30 21:10:32
>> 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... 2025-10-30 21:10:32
>> some scan range may cross Chr bound, trimming... 2025-10-30 21:10:32
>> finding overlap peak in gene scan region... 2025-10-30 21:10:33
>> dealing with left peak not your gene scan region... 2025-10-30 21:10:33
>> merging two set peaks... 2025-10-30 21:10:33
>> calculating distance and dealing with gene strand... 2025-10-30 21:10:33
>> merging all info together ... 2025-10-30 21:10:33
>> done 2025-10-30 21:10:33
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2025-10-30 21:10:34
>> merging all info together... 2025-10-30 21:10:34
>> done 2025-10-30 21:10:34
>> checking seqlevels match... 2025-10-30 21:10:34
>> 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
>> using scanPromoter parameter to scan promoter for each gene... 2025-10-30 21:10:34
>> checking seqlevels match... 2025-10-30 21:10:34
>> 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... 2025-10-30 21:10:36
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene... 2025-10-30 21:10:36
>> checking seqlevels match... 2025-10-30 21:10:36
>> 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... 2025-10-30 21:10:37
>> calculating cor and pvalue, which may be time consuming... 2025-10-30 21:10:37
>> merging all info together... 2025-10-30 21:10:37
>> done 2025-10-30 21:10:37
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
69.876 3.204 73.349
FindIT2.Rcheck/FindIT2-Ex.timings
| name | user | system | elapsed | |
| TF_target_database | 0.000 | 0.000 | 0.001 | |
| calcRP_TFHit | 3.762 | 0.181 | 4.009 | |
| calcRP_coverage | 3.442 | 0.858 | 4.320 | |
| calcRP_region | 4.935 | 0.198 | 5.147 | |
| enhancerPromoterCor | 2.926 | 0.068 | 3.005 | |
| findIT_MARA | 0.489 | 0.014 | 0.503 | |
| findIT_TFHit | 1.052 | 0.019 | 1.073 | |
| findIT_TTPair | 0.080 | 0.006 | 0.087 | |
| findIT_enrichFisher | 0.128 | 0.004 | 0.133 | |
| findIT_enrichWilcox | 0.222 | 0.007 | 0.230 | |
| findIT_regionRP | 6.515 | 0.148 | 6.686 | |
| getAssocPairNumber | 1.412 | 0.051 | 1.471 | |
| integrate_ChIP_RNA | 2.464 | 0.071 | 2.544 | |
| integrate_replicates | 0.002 | 0.000 | 0.002 | |
| jaccard_findIT_TTpair | 0.120 | 0.008 | 0.129 | |
| jaccard_findIT_enrichFisher | 0.205 | 0.003 | 0.209 | |
| loadPeakFile | 0.074 | 0.002 | 0.076 | |
| mm_geneBound | 1.381 | 0.036 | 1.419 | |
| mm_geneScan | 1.449 | 0.046 | 1.500 | |
| mm_nearestGene | 1.159 | 0.028 | 1.190 | |
| peakGeneCor | 3.166 | 0.158 | 3.334 | |
| plot_annoDistance | 1.792 | 0.052 | 1.849 | |
| plot_peakGeneAlias_summary | 1.492 | 0.033 | 1.530 | |
| plot_peakGeneCor | 3.220 | 0.051 | 3.279 | |
| test_geneSet | 0.000 | 0.000 | 0.001 | |