Back to Multiple platform build/check report for BioC 3.21: simplified long |
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This page was generated on 2025-02-04 11:44 -0500 (Tue, 04 Feb 2025).
Hostname | OS | Arch (*) | R version | Installed pkgs |
---|---|---|---|---|
nebbiolo1 | Linux (Ubuntu 24.04.1 LTS) | x86_64 | R Under development (unstable) (2025-01-20 r87609) -- "Unsuffered Consequences" | 4716 |
palomino7 | Windows Server 2022 Datacenter | x64 | R Under development (unstable) (2025-01-21 r87610 ucrt) -- "Unsuffered Consequences" | 4478 |
lconway | macOS 12.7.1 Monterey | x86_64 | R Under development (unstable) (2025-01-22 r87618) -- "Unsuffered Consequences" | 4489 |
kjohnson3 | macOS 13.7.1 Ventura | arm64 | R Under development (unstable) (2025-01-20 r87609) -- "Unsuffered Consequences" | 4442 |
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 715/2295 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||||
FindIT2 1.13.0 (landing page) Guandong Shang
| nebbiolo1 | Linux (Ubuntu 24.04.1 LTS) / x86_64 | OK | OK | OK | |||||||||
palomino7 | Windows Server 2022 Datacenter / x64 | OK | OK | OK | OK | |||||||||
lconway | macOS 12.7.1 Monterey / x86_64 | OK | OK | OK | OK | |||||||||
kjohnson3 | macOS 13.7.1 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: 1.13.0 |
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_1.13.0.tar.gz |
StartedAt: 2025-02-03 19:50:58 -0500 (Mon, 03 Feb 2025) |
EndedAt: 2025-02-03 19:53:09 -0500 (Mon, 03 Feb 2025) |
EllapsedTime: 131.7 seconds |
RetCode: 0 |
Status: OK |
CheckDir: FindIT2.Rcheck |
Warnings: 0 |
############################################################################## ############################################################################## ### ### 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_1.13.0.tar.gz ### ############################################################################## ############################################################################## * using log directory ‘/Users/biocbuild/bbs-3.21-bioc/meat/FindIT2.Rcheck’ * using R Under development (unstable) (2025-01-20 r87609) * using platform: aarch64-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 Ventura 13.7.1 * using session charset: UTF-8 * using option ‘--no-vignettes’ * checking for file ‘FindIT2/DESCRIPTION’ ... OK * this is package ‘FindIT2’ version ‘1.13.0’ * package encoding: UTF-8 * checking package namespace information ... OK * checking package dependencies ... INFO Imports includes 22 non-default packages. Importing from so many packages makes the package vulnerable to any of them becoming unavailable. Move as many as possible to Suggests and use conditionally. * checking if this is a source package ... OK * checking if there is a namespace ... OK * checking for hidden files and directories ... OK * checking for portable file names ... OK * checking for sufficient/correct file permissions ... OK * checking whether package ‘FindIT2’ can be installed ... OK * checking installed package size ... OK * checking package directory ... OK * checking ‘build’ directory ... OK * checking DESCRIPTION meta-information ... OK * checking top-level files ... OK * checking for left-over files ... OK * checking index information ... OK * checking package subdirectories ... 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 * 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-arm64/Resources/library’ * installing *source* package ‘FindIT2’ ... ** this is package ‘FindIT2’ version ‘1.13.0’ ** 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 Under development (unstable) (2025-01-20 r87609) -- "Unsuffered Consequences" Copyright (C) 2025 The R Foundation for Statistical Computing Platform: aarch64-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: GenomeInfoDb > if (!requireNamespace("TxDb.Athaliana.BioMart.plantsmart28")) { + stop("unable to load TxDb.Athaliana.BioMart.plantsmart28") + } Loading required namespace: TxDb.Athaliana.BioMart.plantsmart28 > > test_check("FindIT2") >> preparing gene features information... 2025-02-03 19:52:47 >> some scan range may cross Chr bound, trimming... 2025-02-03 19:52:47 >> preparing weight info... 2025-02-03 19:52:47 >> loading E50h_sampleChr5.bw info... 2025-02-03 19:52:47 ------------ >> extracting and calcluating Chr5 signal... 2025-02-03 19:52:47 >> dealing with Chr5 left gene signal... 2025-02-03 19:52:49 >> norming Chr5RP accoring to the whole Chr RP... 2025-02-03 19:52:49 >> merging all Chr RP together... 2025-02-03 19:52:49 >> done 2025-02-03 19:52:49 >> checking seqlevels match... 2025-02-03 19:52:49 >> your peak_GR seqlevel:Chr5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... Good, your Chrs in peak_GR is all in Txdb ------------ annotatePeak using geneScan mode begins >> preparing gene features information and scan region... 2025-02-03 19:52:49 >> some scan range may cross Chr bound, trimming... 2025-02-03 19:52:50 >> finding overlap peak in gene scan region... 2025-02-03 19:52:50 >> dealing with left peak not your gene scan region... 2025-02-03 19:52:50 >> merging two set peaks... 2025-02-03 19:52:50 >> calculating distance and dealing with gene strand... 2025-02-03 19:52:50 >> merging all info together ... 2025-02-03 19:52:50 >> done 2025-02-03 19:52:50 >> calculating peakCenter to TSS using peak-gene pair... 2025-02-03 19:52:50 >> pre-filling 1356 noAssoc peak gene's RP with 0... 2025-02-03 19:52:50 >> calculating RP using centerToTSS and peak score2025-02-03 19:52:50 >> merging all info together 2025-02-03 19:52:51 >> done 2025-02-03 19:52:51 >> calculating peakCenter to TSS using peak-gene pair... 2025-02-03 19:52:51 >> pre-filling 1356 noAssoc peak gene's RP with 0... 2025-02-03 19:52:51 >> calculating RP using centerToTSS and peak score2025-02-03 19:52:51 >> merging all info together 2025-02-03 19:52:52 >> done 2025-02-03 19:52:52 >> checking seqlevels match... 2025-02-03 19:52:52 >> 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... 2025-02-03 19:52:52 >> some scan range may cross Chr bound, trimming... 2025-02-03 19:52:53 >> finding overlap peak in gene scan region... 2025-02-03 19:52:53 >> dealing with left peak not your gene scan region... 2025-02-03 19:52:53 >> merging two set peaks... 2025-02-03 19:52:53 >> calculating distance and dealing with gene strand... 2025-02-03 19:52:53 >> merging all info together ... 2025-02-03 19:52:53 >> done 2025-02-03 19:52:53 >> calculating peakCenter to TSS using peak-gene pair... 2025-02-03 19:52:53 >> calculating RP using centerToTSS and TF hit 2025-02-03 19:52:53 >> merging all info together 2025-02-03 19:52:53 >> done 2025-02-03 19:52:53 >> calculating peakCenter to TSS using peak-gene pair... 2025-02-03 19:52:53 >> calculating RP using centerToTSS and TF hit 2025-02-03 19:52:54 >> merging all info together 2025-02-03 19:52:54 >> done 2025-02-03 19:52:54 >> checking seqlevels match... 2025-02-03 19:52:54 >> 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 ------------ annotatePeak using geneScan mode begins >> preparing gene features information and scan region... 2025-02-03 19:52:54 >> some scan range may cross Chr bound, trimming... 2025-02-03 19:52:54 >> finding overlap peak in gene scan region... 2025-02-03 19:52:54 >> dealing with left peak not your gene scan region... 2025-02-03 19:52:54 >> merging two set peaks... 2025-02-03 19:52:54 >> calculating distance and dealing with gene strand... 2025-02-03 19:52:54 >> merging all info together ... 2025-02-03 19:52:54 >> done 2025-02-03 19:52:54 >> calculating peakCenter to TSS using peak-gene pair... 2025-02-03 19:52:54 >> pre-filling 1356 noAssoc peak gene's RP with 0... 2025-02-03 19:52:55 >> calculating RP using centerToTSS and peak score2025-02-03 19:52:55 >> merging all info together 2025-02-03 19:52:55 >> done 2025-02-03 19:52:55 >> extracting RP info from regionRP... 2025-02-03 19:52:55 >> dealing with TF_GR_databse... 2025-02-03 19:52:55 >> calculating percent and p-value... 2025-02-03 19:52:56 >> dealing withE5_0h_R1... 2025-02-03 19:52:56 >> dealing withE5_0h_R2... 2025-02-03 19:52:56 >> dealing withE5_4h_R1... 2025-02-03 19:52:56 >> dealing withE5_4h_R2... 2025-02-03 19:52:56 >> dealing withE5_8h_R1... 2025-02-03 19:52:56 >> dealing withE5_8h_R2... 2025-02-03 19:52:56 >> dealing withE5_16h_R1... 2025-02-03 19:52:56 >> dealing withE5_16h_R2... 2025-02-03 19:52:56 >> dealing withE5_24h_R1... 2025-02-03 19:52:56 >> dealing withE5_24h_R2... 2025-02-03 19:52:56 >> dealing withE5_48h_R1... 2025-02-03 19:52:56 >> dealing withE5_48h_R2... 2025-02-03 19:52:56 >> dealing withE5_48h_R3... 2025-02-03 19:52:56 >> dealing withE5_72h_R1... 2025-02-03 19:52:56 >> dealing withE5_72h_R2... 2025-02-03 19:52:56 >> dealing withE5_72h_R3... 2025-02-03 19:52:56 >> merging all info together... 2025-02-03 19:52:56 >> done 2025-02-03 19:52:56 >> preparing gene features information... 2025-02-03 19:52:56 >> some scan range may cross Chr bound, trimming... 2025-02-03 19:52:56 >> calculating p-value for each TF, which may be time consuming... 2025-02-03 19:52:56 >> merging all info together... 2025-02-03 19:52:56 >> done 2025-02-03 19:52:56 >> dealing with TF_GR_database... 2025-02-03 19:52:56 >> calculating coef and converting into z-score using INT... 2025-02-03 19:52:56 >> dealing with E5_0h_R1... 2025-02-03 19:52:56 >> dealing with E5_0h_R2... 2025-02-03 19:52:56 >> dealing with E5_4h_R1... 2025-02-03 19:52:56 >> dealing with E5_4h_R2... 2025-02-03 19:52:56 >> dealing with E5_8h_R1... 2025-02-03 19:52:56 >> dealing with E5_8h_R2... 2025-02-03 19:52:56 >> dealing with E5_16h_R1... 2025-02-03 19:52:56 >> dealing with E5_16h_R2... 2025-02-03 19:52:56 >> dealing with E5_24h_R1... 2025-02-03 19:52:56 >> dealing with E5_24h_R2... 2025-02-03 19:52:56 >> dealing with E5_48h_R1... 2025-02-03 19:52:56 >> dealing with E5_48h_R2... 2025-02-03 19:52:56 >> dealing with E5_48h_R3... 2025-02-03 19:52:56 >> dealing with E5_72h_R1... 2025-02-03 19:52:56 >> dealing with E5_72h_R2... 2025-02-03 19:52:56 >> dealing with E5_72h_R3... 2025-02-03 19:52:56 >> merging all info together... 2025-02-03 19:52:57 >> done 2025-02-03 19:52:57 >> checking seqlevels match... 2025-02-03 19:52:57 >> 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 ------------ annotatePeak using geneScan mode begins >> preparing gene features information and scan region... 2025-02-03 19:52:57 >> some scan range may cross Chr bound, trimming... 2025-02-03 19:52:57 >> finding overlap peak in gene scan region... 2025-02-03 19:52:57 >> dealing with left peak not your gene scan region... 2025-02-03 19:52:57 >> merging two set peaks... 2025-02-03 19:52:57 >> calculating distance and dealing with gene strand... 2025-02-03 19:52:57 >> merging all info together ... 2025-02-03 19:52:57 >> done 2025-02-03 19:52:57 >> calculating peakCenter to TSS using peak-gene pair... 2025-02-03 19:52:57 >> calculating RP using centerToTSS and TF hit 2025-02-03 19:52:57 >> merging all info together 2025-02-03 19:52:57 >> done 2025-02-03 19:52:57 >> checking seqlevels match... 2025-02-03 19:52:57 >> your peak_GR seqlevel:5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... >> checking seqlevels match... 2025-02-03 19:52:57 >> your peak_GR seqlevel:Chr5 Chr6... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... >> checking seqlevels match... 2025-02-03 19:52:58 >> 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... 2025-02-03 19:52:58 >> 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... 2025-02-03 19:52:58 >> finding nearest gene and calculating distance... 2025-02-03 19:52:59 >> dealing with gene strand ... 2025-02-03 19:52:59 >> merging all info together ... 2025-02-03 19:52:59 >> done 2025-02-03 19:52:59 >> checking seqlevels match... 2025-02-03 19:52:59 >> 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... 2025-02-03 19:52:59 >> 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... 2025-02-03 19:52:59 >> finding nearest gene and calculating distance... 2025-02-03 19:52:59 >> dealing with gene strand ... 2025-02-03 19:52:59 >> merging all info together ... 2025-02-03 19:52:59 >> done 2025-02-03 19:52:59 >> checking seqlevels match... 2025-02-03 19:52:59 >> 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... 2025-02-03 19:52:59 >> 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... 2025-02-03 19:52:59 >> finding nearest gene and calculating distance... 2025-02-03 19:53:00 >> dealing with gene strand ... 2025-02-03 19:53:00 >> merging all info together ... 2025-02-03 19:53:00 >> done 2025-02-03 19:53:00 >> checking seqlevels match... 2025-02-03 19:53:00 >> your peak_GR seqlevel:Chr5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... Good, your Chrs in peak_GR is all in Txdb >> checking seqlevels match... 2025-02-03 19:53:00 >> your peak_GR seqlevel:Chr5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... Good, your Chrs in peak_GR is all in Txdb ------------ annotating Peak using nearest gene mode begins >> preparing gene features information... 2025-02-03 19:53:00 >> finding nearest gene and calculating distance... 2025-02-03 19:53:00 >> dealing with gene strand ... 2025-02-03 19:53:00 >> merging all info together ... 2025-02-03 19:53:00 >> done 2025-02-03 19:53:00 It seems that there 1 genes have not been annotated by nearestGene mode >> checking seqlevels match... 2025-02-03 19:53:01 >> 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... 2025-02-03 19:53:01 >> 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... 2025-02-03 19:53:01 >> finding nearest gene and calculating distance... 2025-02-03 19:53:01 >> dealing with gene strand ... 2025-02-03 19:53:01 >> merging all info together ... 2025-02-03 19:53:01 >> done 2025-02-03 19:53:01 It seems that there 1 genes have not been annotated by nearestGene mode >> checking seqlevels match... 2025-02-03 19:53:01 >> 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... 2025-02-03 19:53:01 >> 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... 2025-02-03 19:53:02 >> checking seqlevels match... 2025-02-03 19:53:02 >> your peak_GR seqlevel:Chr5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... Good, your Chrs in peak_GR is all in Txdb >> some scan range may cross Chr bound, trimming... 2025-02-03 19:53:02 Good, your two matrix colnames matchs >> calculating cor and pvalue, which may be time consuming... 2025-02-03 19:53:03 >> merging all info together... 2025-02-03 19:53:03 >> done 2025-02-03 19:53:03 >> checking seqlevels match... 2025-02-03 19:53:03 >> 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 >> using scanPromoter parameter to scan promoter for each gene... 2025-02-03 19:53:03 >> checking seqlevels match... 2025-02-03 19:53:03 >> 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 >> some scan range may cross Chr bound, trimming... 2025-02-03 19:53:03 >> there are 85 gene have scaned promoter >> using scanEnhancer parameter to scan Enhancer for each gene... 2025-02-03 19:53:03 >> checking seqlevels match... 2025-02-03 19:53:03 >> 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 >> some scan range may cross Chr bound, trimming... 2025-02-03 19:53:03 >> calculating cor and pvalue, which may be time consuming... 2025-02-03 19:53:03 >> merging all info together... 2025-02-03 19:53:03 >> done 2025-02-03 19:53:03 Good, your two matrix colnames matchs >> calculating cor and pvalue, which may be time consuming... 2025-02-03 19:53:03 >> merging all info together... 2025-02-03 19:53:03 >> done 2025-02-03 19:53:04 >> checking seqlevels match... 2025-02-03 19:53:04 >> 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 ------------ annotatePeak using geneScan mode begins >> preparing gene features information and scan region... 2025-02-03 19:53:04 >> some scan range may cross Chr bound, trimming... 2025-02-03 19:53:04 >> finding overlap peak in gene scan region... 2025-02-03 19:53:04 >> dealing with left peak not your gene scan region... 2025-02-03 19:53:04 >> merging two set peaks... 2025-02-03 19:53:04 >> calculating distance and dealing with gene strand... 2025-02-03 19:53:04 >> merging all info together ... 2025-02-03 19:53:04 >> done 2025-02-03 19:53:04 Good, your two matrix colnames matchs >> calculating cor and pvalue, which may be time consuming... 2025-02-03 19:53:05 >> merging all info together... 2025-02-03 19:53:05 >> done 2025-02-03 19:53:05 >> checking seqlevels match... 2025-02-03 19:53:05 >> your peak_GR seqlevel:Chr5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... Good, your Chrs in peak_GR is all in Txdb >> using scanPromoter parameter to scan promoter for each gene... 2025-02-03 19:53:05 >> checking seqlevels match... 2025-02-03 19:53:05 >> your peak_GR seqlevel:Chr5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... Good, your Chrs in peak_GR is all in Txdb >> some scan range may cross Chr bound, trimming... 2025-02-03 19:53:05 >> there are 85 gene have scaned promoter >> using scanEnhancer parameter to scan Enhancer for each gene... 2025-02-03 19:53:05 >> checking seqlevels match... 2025-02-03 19:53:05 >> your peak_GR seqlevel:Chr5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... Good, your Chrs in peak_GR is all in Txdb >> some scan range may cross Chr bound, trimming... 2025-02-03 19:53:05 >> calculating cor and pvalue, which may be time consuming... 2025-02-03 19:53:05 >> merging all info together... 2025-02-03 19:53:05 >> done 2025-02-03 19:53:05 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 22.152 1.163 23.451
FindIT2.Rcheck/FindIT2-Ex.timings
name | user | system | elapsed | |
TF_target_database | 0 | 0 | 0 | |
calcRP_TFHit | 1.305 | 0.049 | 1.381 | |
calcRP_coverage | 1.748 | 0.343 | 2.106 | |
calcRP_region | 1.552 | 0.061 | 1.619 | |
enhancerPromoterCor | 0.859 | 0.025 | 0.885 | |
findIT_MARA | 0.139 | 0.004 | 0.141 | |
findIT_TFHit | 0.361 | 0.018 | 0.390 | |
findIT_TTPair | 0.025 | 0.002 | 0.027 | |
findIT_enrichFisher | 0.047 | 0.001 | 0.048 | |
findIT_enrichWilcox | 0.053 | 0.001 | 0.054 | |
findIT_regionRP | 1.960 | 0.068 | 2.092 | |
getAssocPairNumber | 0.389 | 0.016 | 0.407 | |
integrate_ChIP_RNA | 0.711 | 0.039 | 0.753 | |
integrate_replicates | 0.000 | 0.000 | 0.001 | |
jaccard_findIT_TTpair | 0.034 | 0.003 | 0.035 | |
jaccard_findIT_enrichFisher | 0.061 | 0.001 | 0.063 | |
loadPeakFile | 0.017 | 0.001 | 0.018 | |
mm_geneBound | 0.392 | 0.011 | 0.403 | |
mm_geneScan | 0.402 | 0.016 | 0.419 | |
mm_nearestGene | 0.369 | 0.013 | 0.387 | |
peakGeneCor | 0.741 | 0.021 | 0.762 | |
plot_annoDistance | 0.480 | 0.019 | 0.500 | |
plot_peakGeneAlias_summary | 0.831 | 0.035 | 0.881 | |
plot_peakGeneCor | 0.889 | 0.037 | 0.930 | |
test_geneSet | 0.000 | 0.001 | 0.000 | |