Guandong Shang
| Snapshot Date: 2025-10-23 14:17 -0400 (Thu, 23 Oct 2025) |
| git_url: https://git.bioconductor.org/packages/FindIT2 |
| git_branch: devel |
| git_last_commit: 82d0b10 |
| git_last_commit_date: 2025-07-22 19:49:08 -0400 (Tue, 22 Jul 2025) |
| Back to Multiple platform build/check report for BioC 3.22: simplified long |
|
This page was generated on 2025-10-24 12:03 -0400 (Fri, 24 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" | 4898 |
| lconway | macOS 12.7.6 Monterey | x86_64 | 4.5.1 Patched (2025-09-10 r88807) -- "Great Square Root" | 4688 |
| kjohnson3 | macOS 13.7.7 Ventura | arm64 | 4.5.1 Patched (2025-09-10 r88807) -- "Great Square Root" | 4634 |
| taishan | Linux (openEuler 24.03 LTS) | aarch64 | 4.5.0 (2025-04-11) -- "How About a Twenty-Six" | 4658 |
| 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 737/2359 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||||
| FindIT2 1.15.1 (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 | | ||||||||
| taishan | Linux (openEuler 24.03 LTS) / aarch64 | OK | OK | NA | ||||||||||
|
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: 1.15.1 |
| Command: /home/biocbuild/bbs-3.22-bioc/R/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/home/biocbuild/bbs-3.22-bioc/R/site-library --timings FindIT2_1.15.1.tar.gz |
| StartedAt: 2025-10-23 23:35:20 -0400 (Thu, 23 Oct 2025) |
| EndedAt: 2025-10-23 23:42:00 -0400 (Thu, 23 Oct 2025) |
| EllapsedTime: 400.6 seconds |
| RetCode: 0 |
| Status: OK |
| CheckDir: FindIT2.Rcheck |
| Warnings: 0 |
##############################################################################
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###
### Running command:
###
### /home/biocbuild/bbs-3.22-bioc/R/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/home/biocbuild/bbs-3.22-bioc/R/site-library --timings FindIT2_1.15.1.tar.gz
###
##############################################################################
##############################################################################
* using log directory ‘/home/biocbuild/bbs-3.22-bioc/meat/FindIT2.Rcheck’
* using R version 4.5.1 Patched (2025-08-23 r88802)
* 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 ‘1.15.1’
* 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 5.357 0.058 5.416
calcRP_region 5.200 0.109 5.309
* 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
FindIT2.Rcheck/00install.out
############################################################################## ############################################################################## ### ### Running command: ### ### /home/biocbuild/bbs-3.22-bioc/R/bin/R CMD INSTALL FindIT2 ### ############################################################################## ############################################################################## * installing to library ‘/home/biocbuild/bbs-3.22-bioc/R/site-library’ * installing *source* package ‘FindIT2’ ... ** this is package ‘FindIT2’ version ‘1.15.1’ ** 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 (2025-08-23 r88802) -- "Great Square Root"
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... 2025-10-23 23:40:08
>> some scan range may cross Chr bound, trimming... 2025-10-23 23:40:09
>> preparing weight info... 2025-10-23 23:40:09
>> loading E50h_sampleChr5.bw info... 2025-10-23 23:40:09
------------
>> extracting and calcluating Chr5 signal... 2025-10-23 23:40:09
>> dealing with Chr5 left gene signal... 2025-10-23 23:40:12
>> norming Chr5RP accoring to the whole Chr RP... 2025-10-23 23:40:12
>> merging all Chr RP together... 2025-10-23 23:40:12
>> done 2025-10-23 23:40:12
>> checking seqlevels match... 2025-10-23 23:40:12
>> 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
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region... 2025-10-23 23:40:12
>> some scan range may cross Chr bound, trimming... 2025-10-23 23:40:13
>> finding overlap peak in gene scan region... 2025-10-23 23:40:13
>> dealing with left peak not your gene scan region... 2025-10-23 23:40:13
>> merging two set peaks... 2025-10-23 23:40:13
>> calculating distance and dealing with gene strand... 2025-10-23 23:40:14
>> merging all info together ... 2025-10-23 23:40:14
>> done 2025-10-23 23:40:14
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-23 23:40:14
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2025-10-23 23:40:14
>> calculating RP using centerToTSS and peak score2025-10-23 23:40:14
>> merging all info together 2025-10-23 23:40:16
>> done 2025-10-23 23:40:17
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-23 23:40:17
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2025-10-23 23:40:18
>> calculating RP using centerToTSS and peak score2025-10-23 23:40:18
>> merging all info together 2025-10-23 23:40:20
>> done 2025-10-23 23:40:20
>> checking seqlevels match... 2025-10-23 23:40:21
>> 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
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region... 2025-10-23 23:40:21
>> some scan range may cross Chr bound, trimming... 2025-10-23 23:40:21
>> finding overlap peak in gene scan region... 2025-10-23 23:40:21
>> dealing with left peak not your gene scan region... 2025-10-23 23:40:21
>> merging two set peaks... 2025-10-23 23:40:22
>> calculating distance and dealing with gene strand... 2025-10-23 23:40:22
>> merging all info together ... 2025-10-23 23:40:22
>> done 2025-10-23 23:40:22
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-23 23:40:22
>> calculating RP using centerToTSS and TF hit 2025-10-23 23:40:22
>> merging all info together 2025-10-23 23:40:22
>> done 2025-10-23 23:40:22
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-23 23:40:22
>> calculating RP using centerToTSS and TF hit 2025-10-23 23:40:24
>> merging all info together 2025-10-23 23:40:24
>> done 2025-10-23 23:40:24
>> checking seqlevels match... 2025-10-23 23:40:25
>> 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... 2025-10-23 23:40:25
>> some scan range may cross Chr bound, trimming... 2025-10-23 23:40:25
>> finding overlap peak in gene scan region... 2025-10-23 23:40:25
>> dealing with left peak not your gene scan region... 2025-10-23 23:40:25
>> merging two set peaks... 2025-10-23 23:40:26
>> calculating distance and dealing with gene strand... 2025-10-23 23:40:26
>> merging all info together ... 2025-10-23 23:40:26
>> done 2025-10-23 23:40:26
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-23 23:40:26
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2025-10-23 23:40:26
>> calculating RP using centerToTSS and peak score2025-10-23 23:40:26
>> merging all info together 2025-10-23 23:40:28
>> done 2025-10-23 23:40:28
>> extracting RP info from regionRP... 2025-10-23 23:40:29
>> dealing with TF_GR_databse... 2025-10-23 23:40:29
>> calculating percent and p-value... 2025-10-23 23:40:29
>> dealing withE5_0h_R1... 2025-10-23 23:40:29
>> dealing withE5_0h_R2... 2025-10-23 23:40:29
>> dealing withE5_4h_R1... 2025-10-23 23:40:29
>> dealing withE5_4h_R2... 2025-10-23 23:40:29
>> dealing withE5_8h_R1... 2025-10-23 23:40:29
>> dealing withE5_8h_R2... 2025-10-23 23:40:29
>> dealing withE5_16h_R1... 2025-10-23 23:40:29
>> dealing withE5_16h_R2... 2025-10-23 23:40:29
>> dealing withE5_24h_R1... 2025-10-23 23:40:29
>> dealing withE5_24h_R2... 2025-10-23 23:40:30
>> dealing withE5_48h_R1... 2025-10-23 23:40:30
>> dealing withE5_48h_R2... 2025-10-23 23:40:30
>> dealing withE5_48h_R3... 2025-10-23 23:40:30
>> dealing withE5_72h_R1... 2025-10-23 23:40:30
>> dealing withE5_72h_R2... 2025-10-23 23:40:30
>> dealing withE5_72h_R3... 2025-10-23 23:40:30
>> merging all info together... 2025-10-23 23:40:30
>> done 2025-10-23 23:40:30
>> preparing gene features information... 2025-10-23 23:40:30
>> some scan range may cross Chr bound, trimming... 2025-10-23 23:40:31
>> calculating p-value for each TF, which may be time consuming... 2025-10-23 23:40:31
>> merging all info together... 2025-10-23 23:40:31
>> done 2025-10-23 23:40:31
>> dealing with TF_GR_database... 2025-10-23 23:40:31
>> calculating coef and converting into z-score using INT... 2025-10-23 23:40:31
>> dealing with E5_0h_R1... 2025-10-23 23:40:31
>> dealing with E5_0h_R2... 2025-10-23 23:40:31
>> dealing with E5_4h_R1... 2025-10-23 23:40:31
>> dealing with E5_4h_R2... 2025-10-23 23:40:31
>> dealing with E5_8h_R1... 2025-10-23 23:40:31
>> dealing with E5_8h_R2... 2025-10-23 23:40:31
>> dealing with E5_16h_R1... 2025-10-23 23:40:32
>> dealing with E5_16h_R2... 2025-10-23 23:40:32
>> dealing with E5_24h_R1... 2025-10-23 23:40:32
>> dealing with E5_24h_R2... 2025-10-23 23:40:32
>> dealing with E5_48h_R1... 2025-10-23 23:40:32
>> dealing with E5_48h_R2... 2025-10-23 23:40:32
>> dealing with E5_48h_R3... 2025-10-23 23:40:32
>> dealing with E5_72h_R1... 2025-10-23 23:40:32
>> dealing with E5_72h_R2... 2025-10-23 23:40:32
>> dealing with E5_72h_R3... 2025-10-23 23:40:32
>> merging all info together... 2025-10-23 23:40:32
>> done 2025-10-23 23:40:32
>> checking seqlevels match... 2025-10-23 23:40:32
>> 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... 2025-10-23 23:40:32
>> some scan range may cross Chr bound, trimming... 2025-10-23 23:40:34
>> finding overlap peak in gene scan region... 2025-10-23 23:40:34
>> dealing with left peak not your gene scan region... 2025-10-23 23:40:34
>> merging two set peaks... 2025-10-23 23:40:34
>> calculating distance and dealing with gene strand... 2025-10-23 23:40:34
>> merging all info together ... 2025-10-23 23:40:34
>> done 2025-10-23 23:40:34
>> calculating peakCenter to TSS using peak-gene pair... 2025-10-23 23:40:34
>> calculating RP using centerToTSS and TF hit 2025-10-23 23:40:35
>> merging all info together 2025-10-23 23:40:35
>> done 2025-10-23 23:40:35
>> checking seqlevels match... 2025-10-23 23:40:35
>> your peak_GR seqlevel:5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match... 2025-10-23 23:40:36
>> your peak_GR seqlevel:Chr5 Chr6...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match... 2025-10-23 23:40:38
>> 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
>> checking seqlevels match... 2025-10-23 23:40:38
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2025-10-23 23:40:38
>> finding nearest gene and calculating distance... 2025-10-23 23:40:39
>> dealing with gene strand ... 2025-10-23 23:40:39
>> merging all info together ... 2025-10-23 23:40:39
>> done 2025-10-23 23:40:39
>> checking seqlevels match... 2025-10-23 23:40:39
>> 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
>> checking seqlevels match... 2025-10-23 23:40:39
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2025-10-23 23:40:39
>> finding nearest gene and calculating distance... 2025-10-23 23:40:40
>> dealing with gene strand ... 2025-10-23 23:40:40
>> merging all info together ... 2025-10-23 23:40:40
>> done 2025-10-23 23:40:40
>> checking seqlevels match... 2025-10-23 23:40:41
>> 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
>> checking seqlevels match... 2025-10-23 23:40:41
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2025-10-23 23:40:41
>> finding nearest gene and calculating distance... 2025-10-23 23:40:41
>> dealing with gene strand ... 2025-10-23 23:40:41
>> merging all info together ... 2025-10-23 23:40:41
>> done 2025-10-23 23:40:41
>> checking seqlevels match... 2025-10-23 23:40:42
>> 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
>> checking seqlevels match... 2025-10-23 23:40:42
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2025-10-23 23:40:42
>> finding nearest gene and calculating distance... 2025-10-23 23:40:43
>> dealing with gene strand ... 2025-10-23 23:40:43
>> merging all info together ... 2025-10-23 23:40:43
>> done 2025-10-23 23:40:43
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match... 2025-10-23 23:40:44
>> 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
>> checking seqlevels match... 2025-10-23 23:40:44
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2025-10-23 23:40:44
>> finding nearest gene and calculating distance... 2025-10-23 23:40:44
>> dealing with gene strand ... 2025-10-23 23:40:45
>> merging all info together ... 2025-10-23 23:40:45
>> done 2025-10-23 23:40:45
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match... 2025-10-23 23:40:45
>> 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
>> checking seqlevels match... 2025-10-23 23:40:46
>> 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... 2025-10-23 23:40:47
>> checking seqlevels match... 2025-10-23 23:40:48
>> 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... 2025-10-23 23:40:48
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2025-10-23 23:40:50
>> merging all info together... 2025-10-23 23:40:50
>> done 2025-10-23 23:40:50
>> checking seqlevels match... 2025-10-23 23:40:50
>> 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... 2025-10-23 23:40:50
>> checking seqlevels match... 2025-10-23 23:40:50
>> 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... 2025-10-23 23:40:50
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene... 2025-10-23 23:40:51
>> checking seqlevels match... 2025-10-23 23:40:51
>> 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... 2025-10-23 23:40:51
>> calculating cor and pvalue, which may be time consuming... 2025-10-23 23:40:52
>> merging all info together... 2025-10-23 23:40:52
>> done 2025-10-23 23:40:52
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2025-10-23 23:40:52
>> merging all info together... 2025-10-23 23:40:52
>> done 2025-10-23 23:40:52
>> checking seqlevels match... 2025-10-23 23:40:52
>> 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... 2025-10-23 23:40:52
>> some scan range may cross Chr bound, trimming... 2025-10-23 23:40:53
>> finding overlap peak in gene scan region... 2025-10-23 23:40:53
>> dealing with left peak not your gene scan region... 2025-10-23 23:40:53
>> merging two set peaks... 2025-10-23 23:40:53
>> calculating distance and dealing with gene strand... 2025-10-23 23:40:53
>> merging all info together ... 2025-10-23 23:40:53
>> done 2025-10-23 23:40:53
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2025-10-23 23:40:54
>> merging all info together... 2025-10-23 23:40:54
>> done 2025-10-23 23:40:54
>> checking seqlevels match... 2025-10-23 23:40:54
>> 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... 2025-10-23 23:40:54
>> checking seqlevels match... 2025-10-23 23:40:54
>> 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... 2025-10-23 23:40:55
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene... 2025-10-23 23:40:55
>> checking seqlevels match... 2025-10-23 23:40:55
>> 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
>> some scan range may cross Chr bound, trimming... 2025-10-23 23:40:56
>> calculating cor and pvalue, which may be time consuming... 2025-10-23 23:40:56
>> merging all info together... 2025-10-23 23:40:56
>> done 2025-10-23 23:40:56
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
59.783 1.907 61.690
FindIT2.Rcheck/FindIT2-Ex.timings
| name | user | system | elapsed | |
| TF_target_database | 0.000 | 0.001 | 0.000 | |
| calcRP_TFHit | 3.203 | 0.114 | 3.375 | |
| calcRP_coverage | 2.711 | 0.151 | 2.864 | |
| calcRP_region | 5.200 | 0.109 | 5.309 | |
| enhancerPromoterCor | 2.394 | 0.063 | 2.457 | |
| findIT_MARA | 0.397 | 0.005 | 0.403 | |
| findIT_TFHit | 0.817 | 0.001 | 0.818 | |
| findIT_TTPair | 0.066 | 0.001 | 0.067 | |
| findIT_enrichFisher | 0.142 | 0.002 | 0.144 | |
| findIT_enrichWilcox | 0.167 | 0.011 | 0.178 | |
| findIT_regionRP | 5.357 | 0.058 | 5.416 | |
| getAssocPairNumber | 1.058 | 0.014 | 1.073 | |
| integrate_ChIP_RNA | 1.884 | 0.041 | 1.924 | |
| integrate_replicates | 0.002 | 0.000 | 0.002 | |
| jaccard_findIT_TTpair | 0.092 | 0.002 | 0.094 | |
| jaccard_findIT_enrichFisher | 0.191 | 0.002 | 0.192 | |
| loadPeakFile | 0.057 | 0.001 | 0.058 | |
| mm_geneBound | 1.095 | 0.009 | 1.105 | |
| mm_geneScan | 1.099 | 0.003 | 1.102 | |
| mm_nearestGene | 1.004 | 0.003 | 1.006 | |
| peakGeneCor | 2.088 | 0.014 | 2.102 | |
| plot_annoDistance | 1.577 | 0.002 | 1.579 | |
| plot_peakGeneAlias_summary | 2.151 | 0.090 | 2.242 | |
| plot_peakGeneCor | 2.782 | 0.065 | 2.847 | |
| test_geneSet | 0 | 0 | 0 | |