Back to Multiple platform build/check report for BioC 3.18: simplified long |
|
This page was generated on 2024-04-17 11:37:43 -0400 (Wed, 17 Apr 2024).
Hostname | OS | Arch (*) | R version | Installed pkgs |
---|---|---|---|---|
nebbiolo2 | Linux (Ubuntu 22.04.3 LTS) | x86_64 | 4.3.3 (2024-02-29) -- "Angel Food Cake" | 4676 |
palomino4 | Windows Server 2022 Datacenter | x64 | 4.3.3 (2024-02-29 ucrt) -- "Angel Food Cake" | 4414 |
merida1 | macOS 12.7.1 Monterey | x86_64 | 4.3.3 (2024-02-29) -- "Angel Food Cake" | 4437 |
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 711/2266 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||||
FindIT2 1.8.0 (landing page) Guandong Shang
| nebbiolo2 | Linux (Ubuntu 22.04.3 LTS) / x86_64 | OK | OK | OK | |||||||||
palomino4 | Windows Server 2022 Datacenter / x64 | OK | OK | OK | OK | |||||||||
merida1 | macOS 12.7.1 Monterey / x86_64 | OK | OK | OK | OK | |||||||||
kjohnson1 | macOS 13.6.1 Ventura / arm64 | see weekly results here | ||||||||||||
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: 1.8.0 |
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_1.8.0.tar.gz |
StartedAt: 2024-04-16 02:49:07 -0400 (Tue, 16 Apr 2024) |
EndedAt: 2024-04-16 03:01:27 -0400 (Tue, 16 Apr 2024) |
EllapsedTime: 740.7 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_1.8.0.tar.gz ### ############################################################################## ############################################################################## * using log directory ‘/Users/biocbuild/bbs-3.18-bioc/meat/FindIT2.Rcheck’ * using R version 4.3.3 (2024-02-29) * using platform: x86_64-apple-darwin20 (64-bit) * R was compiled by Apple clang version 14.0.0 (clang-1400.0.29.202) GNU Fortran (GCC) 12.2.0 * running under: macOS Monterey 12.7.1 * using session charset: UTF-8 * using option ‘--no-vignettes’ * checking for file ‘FindIT2/DESCRIPTION’ ... OK * this is package ‘FindIT2’ version ‘1.8.0’ * package encoding: UTF-8 * checking package namespace information ... OK * checking package dependencies ... OK * 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 R files for non-ASCII characters ... OK * checking R files for syntax errors ... OK * checking whether the package can be loaded ... OK * checking whether the package can be loaded with stated dependencies ... OK * checking whether the package can be unloaded cleanly ... OK * checking whether the namespace can be loaded with stated dependencies ... OK * checking whether the namespace can be unloaded cleanly ... OK * checking dependencies in R code ... OK * checking S3 generic/method consistency ... OK * checking replacement functions ... OK * checking foreign function calls ... OK * checking R code for possible problems ... OK * checking Rd files ... OK * checking Rd metadata ... OK * checking Rd cross-references ... OK * checking for missing documentation entries ... OK * checking for code/documentation mismatches ... OK * checking Rd \usage sections ... OK * checking Rd contents ... OK * checking for unstated dependencies in examples ... OK * checking contents of ‘data’ directory ... OK * checking data for non-ASCII characters ... OK * checking data for ASCII and uncompressed saves ... OK * checking files in ‘vignettes’ ... OK * checking examples ... OK Examples with CPU (user + system) or elapsed time > 5s user system elapsed findIT_regionRP 11.827 0.167 13.344 calcRP_region 9.640 0.205 10.371 plot_peakGeneCor 7.277 0.124 7.446 calcRP_coverage 6.366 0.788 7.281 calcRP_TFHit 6.496 0.294 7.214 enhancerPromoterCor 5.375 0.108 6.268 peakGeneCor 5.267 0.186 5.714 integrate_ChIP_RNA 4.994 0.085 5.958 * checking for unstated dependencies in ‘tests’ ... OK * checking tests ... Running ‘testthat.R’ OK * checking for unstated dependencies in vignettes ... OK * checking package vignettes in ‘inst/doc’ ... 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/4.3-x86_64/Resources/library’ * installing *source* package ‘FindIT2’ ... ** 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 4.3.3 (2024-02-29) -- "Angel Food Cake" Copyright (C) 2024 The R Foundation for Statistical Computing Platform: x86_64-apple-darwin20 (64-bit) 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 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, intersect, is.unsorted, lapply, mapply, match, mget, order, paste, pmax, pmax.int, pmin, pmin.int, rank, rbind, rownames, sapply, setdiff, sort, table, tapply, union, 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... 2024-04-16 02:59:22 >> some scan range may cross Chr bound, trimming... 2024-04-16 02:59:25 >> preparing weight info... 2024-04-16 02:59:25 >> loading E50h_sampleChr5.bw info... 2024-04-16 02:59:25 ------------ >> extracting and calcluating Chr5 signal... 2024-04-16 02:59:25 >> dealing with Chr5 left gene signal... 2024-04-16 02:59:31 >> norming Chr5RP accoring to the whole Chr RP... 2024-04-16 02:59:31 >> merging all Chr RP together... 2024-04-16 02:59:31 >> done 2024-04-16 02:59:31 >> checking seqlevels match... 2024-04-16 02:59:31 >> 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... 2024-04-16 02:59:31 >> some scan range may cross Chr bound, trimming... 2024-04-16 02:59:33 >> finding overlap peak in gene scan region... 2024-04-16 02:59:33 >> dealing with left peak not your gene scan region... 2024-04-16 02:59:33 >> merging two set peaks... 2024-04-16 02:59:33 >> calculating distance and dealing with gene strand... 2024-04-16 02:59:34 >> merging all info together ... 2024-04-16 02:59:34 >> done 2024-04-16 02:59:34 >> calculating peakCenter to TSS using peak-gene pair... 2024-04-16 02:59:34 >> pre-filling 1356 noAssoc peak gene's RP with 0... 2024-04-16 02:59:35 >> calculating RP using centerToTSS and peak score2024-04-16 02:59:35 >> merging all info together 2024-04-16 02:59:40 >> done 2024-04-16 02:59:42 >> calculating peakCenter to TSS using peak-gene pair... 2024-04-16 02:59:42 >> pre-filling 1356 noAssoc peak gene's RP with 0... 2024-04-16 02:59:43 >> calculating RP using centerToTSS and peak score2024-04-16 02:59:43 >> merging all info together 2024-04-16 02:59:49 >> done 2024-04-16 02:59:49 >> checking seqlevels match... 2024-04-16 02:59:50 >> 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 ------------ annotatePeak using geneScan mode begins >> preparing gene features information and scan region... 2024-04-16 02:59:50 >> some scan range may cross Chr bound, trimming... 2024-04-16 02:59:51 >> finding overlap peak in gene scan region... 2024-04-16 02:59:51 >> dealing with left peak not your gene scan region... 2024-04-16 02:59:52 >> merging two set peaks... 2024-04-16 02:59:52 >> calculating distance and dealing with gene strand... 2024-04-16 02:59:52 >> merging all info together ... 2024-04-16 02:59:52 >> done 2024-04-16 02:59:52 >> calculating peakCenter to TSS using peak-gene pair... 2024-04-16 02:59:52 >> calculating RP using centerToTSS and TF hit 2024-04-16 02:59:54 >> merging all info together 2024-04-16 02:59:54 >> done 2024-04-16 02:59:54 >> calculating peakCenter to TSS using peak-gene pair... 2024-04-16 02:59:54 >> calculating RP using centerToTSS and TF hit 2024-04-16 02:59:56 >> merging all info together 2024-04-16 02:59:56 >> done 2024-04-16 02:59:56 >> checking seqlevels match... 2024-04-16 02:59:58 >> 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 ------------ annotatePeak using geneScan mode begins >> preparing gene features information and scan region... 2024-04-16 02:59:58 >> some scan range may cross Chr bound, trimming... 2024-04-16 03:00:00 >> finding overlap peak in gene scan region... 2024-04-16 03:00:00 >> dealing with left peak not your gene scan region... 2024-04-16 03:00:00 >> merging two set peaks... 2024-04-16 03:00:01 >> calculating distance and dealing with gene strand... 2024-04-16 03:00:01 >> merging all info together ... 2024-04-16 03:00:01 >> done 2024-04-16 03:00:01 >> calculating peakCenter to TSS using peak-gene pair... 2024-04-16 03:00:01 >> pre-filling 1356 noAssoc peak gene's RP with 0... 2024-04-16 03:00:03 >> calculating RP using centerToTSS and peak score2024-04-16 03:00:03 >> merging all info together 2024-04-16 03:00:07 >> done 2024-04-16 03:00:08 >> extracting RP info from regionRP... 2024-04-16 03:00:09 >> dealing with TF_GR_databse... 2024-04-16 03:00:09 >> calculating percent and p-value... 2024-04-16 03:00:09 >> dealing withE5_0h_R1... 2024-04-16 03:00:09 >> dealing withE5_0h_R2... 2024-04-16 03:00:09 >> dealing withE5_4h_R1... 2024-04-16 03:00:09 >> dealing withE5_4h_R2... 2024-04-16 03:00:10 >> dealing withE5_8h_R1... 2024-04-16 03:00:10 >> dealing withE5_8h_R2... 2024-04-16 03:00:10 >> dealing withE5_16h_R1... 2024-04-16 03:00:10 >> dealing withE5_16h_R2... 2024-04-16 03:00:10 >> dealing withE5_24h_R1... 2024-04-16 03:00:10 >> dealing withE5_24h_R2... 2024-04-16 03:00:10 >> dealing withE5_48h_R1... 2024-04-16 03:00:10 >> dealing withE5_48h_R2... 2024-04-16 03:00:10 >> dealing withE5_48h_R3... 2024-04-16 03:00:10 >> dealing withE5_72h_R1... 2024-04-16 03:00:11 >> dealing withE5_72h_R2... 2024-04-16 03:00:11 >> dealing withE5_72h_R3... 2024-04-16 03:00:11 >> merging all info together... 2024-04-16 03:00:11 >> done 2024-04-16 03:00:11 >> preparing gene features information... 2024-04-16 03:00:11 >> some scan range may cross Chr bound, trimming... 2024-04-16 03:00:13 >> calculating p-value for each TF, which may be time consuming... 2024-04-16 03:00:13 >> merging all info together... 2024-04-16 03:00:13 >> done 2024-04-16 03:00:13 >> dealing with TF_GR_database... 2024-04-16 03:00:14 >> calculating coef and converting into z-score using INT... 2024-04-16 03:00:14 >> dealing with E5_0h_R1... 2024-04-16 03:00:14 >> dealing with E5_0h_R2... 2024-04-16 03:00:14 >> dealing with E5_4h_R1... 2024-04-16 03:00:14 >> dealing with E5_4h_R2... 2024-04-16 03:00:15 >> dealing with E5_8h_R1... 2024-04-16 03:00:15 >> dealing with E5_8h_R2... 2024-04-16 03:00:15 >> dealing with E5_16h_R1... 2024-04-16 03:00:15 >> dealing with E5_16h_R2... 2024-04-16 03:00:15 >> dealing with E5_24h_R1... 2024-04-16 03:00:15 >> dealing with E5_24h_R2... 2024-04-16 03:00:16 >> dealing with E5_48h_R1... 2024-04-16 03:00:16 >> dealing with E5_48h_R2... 2024-04-16 03:00:16 >> dealing with E5_48h_R3... 2024-04-16 03:00:16 >> dealing with E5_72h_R1... 2024-04-16 03:00:16 >> dealing with E5_72h_R2... 2024-04-16 03:00:17 >> dealing with E5_72h_R3... 2024-04-16 03:00:17 >> merging all info together... 2024-04-16 03:00:17 >> done 2024-04-16 03:00:17 >> checking seqlevels match... 2024-04-16 03:00:18 >> 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 ------------ annotatePeak using geneScan mode begins >> preparing gene features information and scan region... 2024-04-16 03:00:18 >> some scan range may cross Chr bound, trimming... 2024-04-16 03:00:19 >> finding overlap peak in gene scan region... 2024-04-16 03:00:19 >> dealing with left peak not your gene scan region... 2024-04-16 03:00:19 >> merging two set peaks... 2024-04-16 03:00:20 >> calculating distance and dealing with gene strand... 2024-04-16 03:00:20 >> merging all info together ... 2024-04-16 03:00:20 >> done 2024-04-16 03:00:20 >> calculating peakCenter to TSS using peak-gene pair... 2024-04-16 03:00:20 >> calculating RP using centerToTSS and TF hit 2024-04-16 03:00:21 >> merging all info together 2024-04-16 03:00:21 >> done 2024-04-16 03:00:22 >> checking seqlevels match... 2024-04-16 03:00:22 >> your peak_GR seqlevel:5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... >> checking seqlevels match... 2024-04-16 03:00:22 >> your peak_GR seqlevel:Chr5 Chr6... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... >> checking seqlevels match... 2024-04-16 03:00:29 >> 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... 2024-04-16 03:00:29 >> 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... 2024-04-16 03:00:29 >> finding nearest gene and calculating distance... 2024-04-16 03:00:31 >> dealing with gene strand ... 2024-04-16 03:00:31 >> merging all info together ... 2024-04-16 03:00:31 >> done 2024-04-16 03:00:31 >> checking seqlevels match... 2024-04-16 03:00:31 >> 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... 2024-04-16 03:00:31 >> 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... 2024-04-16 03:00:32 >> finding nearest gene and calculating distance... 2024-04-16 03:00:33 >> dealing with gene strand ... 2024-04-16 03:00:33 >> merging all info together ... 2024-04-16 03:00:33 >> done 2024-04-16 03:00:33 >> checking seqlevels match... 2024-04-16 03:00:35 >> 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... 2024-04-16 03:00:35 >> 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... 2024-04-16 03:00:35 >> finding nearest gene and calculating distance... 2024-04-16 03:00:37 >> dealing with gene strand ... 2024-04-16 03:00:37 >> merging all info together ... 2024-04-16 03:00:37 >> done 2024-04-16 03:00:37 >> checking seqlevels match... 2024-04-16 03:00:39 >> 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... 2024-04-16 03:00:39 >> 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... 2024-04-16 03:00:39 >> finding nearest gene and calculating distance... 2024-04-16 03:00:40 >> dealing with gene strand ... 2024-04-16 03:00:41 >> merging all info together ... 2024-04-16 03:00:41 >> done 2024-04-16 03:00:41 It seems that there 1 genes have not been annotated by nearestGene mode >> checking seqlevels match... 2024-04-16 03:00:42 >> 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... 2024-04-16 03:00:43 >> 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... 2024-04-16 03:00:43 >> finding nearest gene and calculating distance... 2024-04-16 03:00:44 >> dealing with gene strand ... 2024-04-16 03:00:44 >> merging all info together ... 2024-04-16 03:00:44 >> done 2024-04-16 03:00:44 It seems that there 1 genes have not been annotated by nearestGene mode >> checking seqlevels match... 2024-04-16 03:00:46 >> 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 >> checking seqlevels match... 2024-04-16 03:00:48 >> 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... 2024-04-16 03:00:49 >> checking seqlevels match... 2024-04-16 03:00:51 >> 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... 2024-04-16 03:00:52 Good, your two matrix colnames matchs >> calculating cor and pvalue, which may be time consuming... 2024-04-16 03:00:56 >> merging all info together... 2024-04-16 03:00:56 >> done 2024-04-16 03:00:56 >> checking seqlevels match... 2024-04-16 03:00:56 >> your peak_GR seqlevel:Chr5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... Good, your Chrs in peak_GR is all in Txdb >> using scanPromoter parameter to scan promoter for each gene... 2024-04-16 03:00:56 >> checking seqlevels match... 2024-04-16 03:00:56 >> your peak_GR seqlevel:Chr5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... Good, your Chrs in peak_GR is all in Txdb >> some scan range may cross Chr bound, trimming... 2024-04-16 03:00:58 >> there are 85 gene have scaned promoter >> using scanEnhancer parameter to scan Enhancer for each gene... 2024-04-16 03:00:58 >> checking seqlevels match... 2024-04-16 03:00:58 >> 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 >> some scan range may cross Chr bound, trimming... 2024-04-16 03:01:00 >> calculating cor and pvalue, which may be time consuming... 2024-04-16 03:01:00 >> merging all info together... 2024-04-16 03:01:01 >> done 2024-04-16 03:01:01 Good, your two matrix colnames matchs >> calculating cor and pvalue, which may be time consuming... 2024-04-16 03:01:01 >> merging all info together... 2024-04-16 03:01:01 >> done 2024-04-16 03:01:01 >> checking seqlevels match... 2024-04-16 03:01:02 >> 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 ------------ annotatePeak using geneScan mode begins >> preparing gene features information and scan region... 2024-04-16 03:01:02 >> some scan range may cross Chr bound, trimming... 2024-04-16 03:01:03 >> finding overlap peak in gene scan region... 2024-04-16 03:01:03 >> dealing with left peak not your gene scan region... 2024-04-16 03:01:03 >> merging two set peaks... 2024-04-16 03:01:04 >> calculating distance and dealing with gene strand... 2024-04-16 03:01:04 >> merging all info together ... 2024-04-16 03:01:04 >> done 2024-04-16 03:01:04 Good, your two matrix colnames matchs >> calculating cor and pvalue, which may be time consuming... 2024-04-16 03:01:07 >> merging all info together... 2024-04-16 03:01:07 >> done 2024-04-16 03:01:07 >> checking seqlevels match... 2024-04-16 03:01:07 >> 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 >> using scanPromoter parameter to scan promoter for each gene... 2024-04-16 03:01:07 >> checking seqlevels match... 2024-04-16 03:01:07 >> 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 >> some scan range may cross Chr bound, trimming... 2024-04-16 03:01:09 >> there are 85 gene have scaned promoter >> using scanEnhancer parameter to scan Enhancer for each gene... 2024-04-16 03:01:09 >> checking seqlevels match... 2024-04-16 03:01:09 >> 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 >> some scan range may cross Chr bound, trimming... 2024-04-16 03:01:11 >> calculating cor and pvalue, which may be time consuming... 2024-04-16 03:01:11 >> merging all info together... 2024-04-16 03:01:12 >> done 2024-04-16 03:01:12 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 125.827 3.823 136.271
FindIT2.Rcheck/FindIT2-Ex.timings
name | user | system | elapsed | |
TF_target_database | 0.001 | 0.002 | 0.001 | |
calcRP_TFHit | 6.496 | 0.294 | 7.214 | |
calcRP_coverage | 6.366 | 0.788 | 7.281 | |
calcRP_region | 9.640 | 0.205 | 10.371 | |
enhancerPromoterCor | 5.375 | 0.108 | 6.268 | |
findIT_MARA | 0.955 | 0.030 | 1.085 | |
findIT_TFHit | 1.818 | 0.037 | 2.076 | |
findIT_TTPair | 0.149 | 0.007 | 0.173 | |
findIT_enrichFisher | 0.340 | 0.008 | 0.406 | |
findIT_enrichWilcox | 0.370 | 0.008 | 0.410 | |
findIT_regionRP | 11.827 | 0.167 | 13.344 | |
getAssocPairNumber | 2.304 | 0.035 | 2.640 | |
integrate_ChIP_RNA | 4.994 | 0.085 | 5.958 | |
integrate_replicates | 0.004 | 0.001 | 0.006 | |
jaccard_findIT_TTpair | 0.197 | 0.010 | 0.232 | |
jaccard_findIT_enrichFisher | 0.419 | 0.008 | 0.458 | |
loadPeakFile | 0.126 | 0.003 | 0.143 | |
mm_geneBound | 2.308 | 0.041 | 2.552 | |
mm_geneScan | 2.356 | 0.045 | 2.528 | |
mm_nearestGene | 2.070 | 0.044 | 2.199 | |
peakGeneCor | 5.267 | 0.186 | 5.714 | |
plot_annoDistance | 2.971 | 0.090 | 3.195 | |
plot_peakGeneAlias_summary | 2.546 | 0.050 | 2.604 | |
plot_peakGeneCor | 7.277 | 0.124 | 7.446 | |
test_geneSet | 0.000 | 0.001 | 0.001 | |