Back to Build/check report for BioC 3.17 |
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This page was generated on 2023-01-29 16:33:47 -0000 (Sun, 29 Jan 2023).
Hostname | OS | Arch (*) | R version | Installed pkgs |
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kunpeng1 | Linux (Ubuntu 22.04.1 LTS) | aarch64 | R Under development (unstable) (2023-01-14 r83615) -- "Unsuffered Consequences" | 4021 |
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To the developers/maintainers of the FindIT2 package: - Please 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 How and When does the builder pull? When will my changes propagate? for more information. - Make sure to use the following settings in order to reproduce any error or warning you see on this page. |
Package 668/2162 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||||
FindIT2 1.5.0 (landing page) Guandong Shang
| kunpeng1 | Linux (Ubuntu 22.04.1 LTS) / aarch64 | OK | OK | WARNINGS | |||||||||
Package: FindIT2 |
Version: 1.5.0 |
Command: /home/biocbuild/bbs-3.17-bioc/R/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/home/biocbuild/bbs-3.17-bioc/R/library --timings FindIT2_1.5.0.tar.gz |
StartedAt: 2023-01-28 22:58:09 -0000 (Sat, 28 Jan 2023) |
EndedAt: 2023-01-28 23:06:02 -0000 (Sat, 28 Jan 2023) |
EllapsedTime: 473.1 seconds |
RetCode: 0 |
Status: WARNINGS |
CheckDir: FindIT2.Rcheck |
Warnings: 2 |
############################################################################## ############################################################################## ### ### Running command: ### ### /home/biocbuild/bbs-3.17-bioc/R/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/home/biocbuild/bbs-3.17-bioc/R/library --timings FindIT2_1.5.0.tar.gz ### ############################################################################## ############################################################################## * using log directory ‘/home/biocbuild/bbs-3.17-bioc/meat/FindIT2.Rcheck’ * using R Under development (unstable) (2023-01-14 r83615) * using platform: aarch64-unknown-linux-gnu (64-bit) * R was compiled by gcc (Ubuntu 11.3.0-1ubuntu1~22.04) 11.3.0 GNU Fortran (Ubuntu 11.3.0-1ubuntu1~22.04) 11.3.0 * running under: Ubuntu 22.04.1 LTS * using session charset: UTF-8 * checking for file ‘FindIT2/DESCRIPTION’ ... OK * this is package ‘FindIT2’ version ‘1.5.0’ * 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 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 ... WARNING Invalid citation information in ‘inst/CITATION’: Warning message: In utils::packageDescription(basename(dir), dirname(dir)) : no package 'FindIT2' was found * 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 loading without being on the library search path ... WARNING Error in library(FindIT2, lib.loc = "/home/biocbuild/bbs-3.17-bioc/R/library") : there is no package called ‘FindIT2’ Execution halted It looks like this package has a loading problem when not on .libPaths: see the messages for details. * 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 ... SKIPPED * 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 ... ‘FindIT2.Rmd’ using ‘UTF-8’... OK NONE * checking re-building of vignette outputs ... OK * checking PDF version of manual ... OK * DONE Status: 2 WARNINGs See ‘/home/biocbuild/bbs-3.17-bioc/meat/FindIT2.Rcheck/00check.log’ for details.
FindIT2.Rcheck/00install.out
############################################################################## ############################################################################## ### ### Running command: ### ### /home/biocbuild/bbs-3.17-bioc/R/bin/R CMD INSTALL FindIT2 ### ############################################################################## ############################################################################## * installing to library ‘/home/biocbuild/bbs-3.17-bioc/R/site-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 Under development (unstable) (2023-01-14 r83615) -- "Unsuffered Consequences" Copyright (C) 2023 The R Foundation for Statistical Computing Platform: aarch64-unknown-linux-gnu (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 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... 2023-01-28 23:02:48 >> some scan range may cross Chr bound, trimming... 2023-01-28 23:02:50 >> preparing weight info... 2023-01-28 23:02:50 >> loading E50h_sampleChr5.bw info... 2023-01-28 23:02:50 ------------ >> extracting and calcluating Chr5 signal... 2023-01-28 23:02:51 >> dealing with Chr5 left gene signal... 2023-01-28 23:03:00 >> norming Chr5RP accoring to the whole Chr RP... 2023-01-28 23:03:00 >> merging all Chr RP together... 2023-01-28 23:03:00 >> done 2023-01-28 23:03:00 >> checking seqlevels match... 2023-01-28 23:03:00 >> 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 ------------ annotatePeak using geneScan mode begins >> preparing gene features information and scan region... 2023-01-28 23:03:00 >> some scan range may cross Chr bound, trimming... 2023-01-28 23:03:01 >> finding overlap peak in gene scan region... 2023-01-28 23:03:01 >> dealing with left peak not your gene scan region... 2023-01-28 23:03:01 >> merging two set peaks... 2023-01-28 23:03:02 >> calculating distance and dealing with gene strand... 2023-01-28 23:03:02 >> merging all info together ... 2023-01-28 23:03:02 >> done 2023-01-28 23:03:02 >> calculating peakCenter to TSS using peak-gene pair... 2023-01-28 23:03:02 >> pre-filling 1356 noAssoc peak gene's RP with 0... 2023-01-28 23:03:03 >> calculating RP using centerToTSS and peak score2023-01-28 23:03:03 >> merging all info together 2023-01-28 23:03:06 >> done 2023-01-28 23:03:07 >> calculating peakCenter to TSS using peak-gene pair... 2023-01-28 23:03:07 >> pre-filling 1356 noAssoc peak gene's RP with 0... 2023-01-28 23:03:08 >> calculating RP using centerToTSS and peak score2023-01-28 23:03:08 >> merging all info together 2023-01-28 23:03:12 >> done 2023-01-28 23:03:13 >> checking seqlevels match... 2023-01-28 23:03:13 >> 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... 2023-01-28 23:03:13 >> some scan range may cross Chr bound, trimming... 2023-01-28 23:03:14 >> finding overlap peak in gene scan region... 2023-01-28 23:03:14 >> dealing with left peak not your gene scan region... 2023-01-28 23:03:14 >> merging two set peaks... 2023-01-28 23:03:15 >> calculating distance and dealing with gene strand... 2023-01-28 23:03:15 >> merging all info together ... 2023-01-28 23:03:15 >> done 2023-01-28 23:03:15 >> calculating peakCenter to TSS using peak-gene pair... 2023-01-28 23:03:15 >> calculating RP using centerToTSS and TF hit 2023-01-28 23:03:16 >> merging all info together 2023-01-28 23:03:16 >> done 2023-01-28 23:03:16 >> calculating peakCenter to TSS using peak-gene pair... 2023-01-28 23:03:16 >> calculating RP using centerToTSS and TF hit 2023-01-28 23:03:17 >> merging all info together 2023-01-28 23:03:17 >> done 2023-01-28 23:03:17 >> checking seqlevels match... 2023-01-28 23:03:18 >> 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... 2023-01-28 23:03:18 >> some scan range may cross Chr bound, trimming... 2023-01-28 23:03:19 >> finding overlap peak in gene scan region... 2023-01-28 23:03:19 >> dealing with left peak not your gene scan region... 2023-01-28 23:03:19 >> merging two set peaks... 2023-01-28 23:03:19 >> calculating distance and dealing with gene strand... 2023-01-28 23:03:20 >> merging all info together ... 2023-01-28 23:03:20 >> done 2023-01-28 23:03:20 >> calculating peakCenter to TSS using peak-gene pair... 2023-01-28 23:03:20 >> pre-filling 1356 noAssoc peak gene's RP with 0... 2023-01-28 23:03:21 >> calculating RP using centerToTSS and peak score2023-01-28 23:03:21 >> merging all info together 2023-01-28 23:03:24 >> done 2023-01-28 23:03:24 >> extracting RP info from regionRP... 2023-01-28 23:03:26 >> dealing with TF_GR_databse... 2023-01-28 23:03:26 >> calculating percent and p-value... 2023-01-28 23:03:26 >> dealing withE5_0h_R1... 2023-01-28 23:03:26 >> dealing withE5_0h_R2... 2023-01-28 23:03:26 >> dealing withE5_4h_R1... 2023-01-28 23:03:26 >> dealing withE5_4h_R2... 2023-01-28 23:03:26 >> dealing withE5_8h_R1... 2023-01-28 23:03:27 >> dealing withE5_8h_R2... 2023-01-28 23:03:27 >> dealing withE5_16h_R1... 2023-01-28 23:03:27 >> dealing withE5_16h_R2... 2023-01-28 23:03:27 >> dealing withE5_24h_R1... 2023-01-28 23:03:27 >> dealing withE5_24h_R2... 2023-01-28 23:03:27 >> dealing withE5_48h_R1... 2023-01-28 23:03:27 >> dealing withE5_48h_R2... 2023-01-28 23:03:27 >> dealing withE5_48h_R3... 2023-01-28 23:03:27 >> dealing withE5_72h_R1... 2023-01-28 23:03:27 >> dealing withE5_72h_R2... 2023-01-28 23:03:27 >> dealing withE5_72h_R3... 2023-01-28 23:03:27 >> merging all info together... 2023-01-28 23:03:27 >> done 2023-01-28 23:03:27 >> preparing gene features information... 2023-01-28 23:03:28 >> some scan range may cross Chr bound, trimming... 2023-01-28 23:03:29 >> calculating p-value for each TF, which may be time consuming... 2023-01-28 23:03:29 >> merging all info together... 2023-01-28 23:03:29 >> done 2023-01-28 23:03:29 >> dealing with TF_GR_database... 2023-01-28 23:03:29 >> calculating coef and converting into z-score using INT... 2023-01-28 23:03:29 >> dealing with E5_0h_R1... 2023-01-28 23:03:29 >> dealing with E5_0h_R2... 2023-01-28 23:03:30 >> dealing with E5_4h_R1... 2023-01-28 23:03:30 >> dealing with E5_4h_R2... 2023-01-28 23:03:30 >> dealing with E5_8h_R1... 2023-01-28 23:03:30 >> dealing with E5_8h_R2... 2023-01-28 23:03:30 >> dealing with E5_16h_R1... 2023-01-28 23:03:30 >> dealing with E5_16h_R2... 2023-01-28 23:03:30 >> dealing with E5_24h_R1... 2023-01-28 23:03:30 >> dealing with E5_24h_R2... 2023-01-28 23:03:30 >> dealing with E5_48h_R1... 2023-01-28 23:03:31 >> dealing with E5_48h_R2... 2023-01-28 23:03:31 >> dealing with E5_48h_R3... 2023-01-28 23:03:31 >> dealing with E5_72h_R1... 2023-01-28 23:03:31 >> dealing with E5_72h_R2... 2023-01-28 23:03:31 >> dealing with E5_72h_R3... 2023-01-28 23:03:31 >> merging all info together... 2023-01-28 23:03:31 >> done 2023-01-28 23:03:31 >> checking seqlevels match... 2023-01-28 23:03:31 >> 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... 2023-01-28 23:03:32 >> some scan range may cross Chr bound, trimming... 2023-01-28 23:03:33 >> finding overlap peak in gene scan region... 2023-01-28 23:03:33 >> dealing with left peak not your gene scan region... 2023-01-28 23:03:33 >> merging two set peaks... 2023-01-28 23:03:33 >> calculating distance and dealing with gene strand... 2023-01-28 23:03:33 >> merging all info together ... 2023-01-28 23:03:33 >> done 2023-01-28 23:03:33 >> calculating peakCenter to TSS using peak-gene pair... 2023-01-28 23:03:33 >> calculating RP using centerToTSS and TF hit 2023-01-28 23:03:34 >> merging all info together 2023-01-28 23:03:34 >> done 2023-01-28 23:03:34 >> checking seqlevels match... 2023-01-28 23:03:35 >> your peak_GR seqlevel:5... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... >> checking seqlevels match... 2023-01-28 23:03:35 >> your peak_GR seqlevel:Chr5 Chr6... >> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC... >> checking seqlevels match... 2023-01-28 23:03:39 >> 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... 2023-01-28 23:03:39 >> 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... 2023-01-28 23:03:39 >> finding nearest gene and calculating distance... 2023-01-28 23:03:40 >> dealing with gene strand ... 2023-01-28 23:03:40 >> merging all info together ... 2023-01-28 23:03:40 >> done 2023-01-28 23:03:40 >> checking seqlevels match... 2023-01-28 23:03:40 >> 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... 2023-01-28 23:03:41 >> 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... 2023-01-28 23:03:41 >> finding nearest gene and calculating distance... 2023-01-28 23:03:43 >> dealing with gene strand ... 2023-01-28 23:03:43 >> merging all info together ... 2023-01-28 23:03:43 >> done 2023-01-28 23:03:43 >> checking seqlevels match... 2023-01-28 23:03:44 >> 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... 2023-01-28 23:03:44 >> 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... 2023-01-28 23:03:44 >> finding nearest gene and calculating distance... 2023-01-28 23:03:45 >> dealing with gene strand ... 2023-01-28 23:03:45 >> merging all info together ... 2023-01-28 23:03:45 >> done 2023-01-28 23:03:45 >> checking seqlevels match... 2023-01-28 23:03:46 >> 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... 2023-01-28 23:03:46 >> 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 ------------ annotating Peak using nearest gene mode begins >> preparing gene features information... 2023-01-28 23:03:46 >> finding nearest gene and calculating distance... 2023-01-28 23:03:47 >> dealing with gene strand ... 2023-01-28 23:03:48 >> merging all info together ... 2023-01-28 23:03:48 >> done 2023-01-28 23:03:48 It seems that there 1 genes have not been annotated by nearestGene mode >> checking seqlevels match... 2023-01-28 23:03:49 >> 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 >> checking seqlevels match... 2023-01-28 23:03:49 >> 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 ------------ annotating Peak using nearest gene mode begins >> preparing gene features information... 2023-01-28 23:03:49 >> finding nearest gene and calculating distance... 2023-01-28 23:03:50 >> dealing with gene strand ... 2023-01-28 23:03:50 >> merging all info together ... 2023-01-28 23:03:50 >> done 2023-01-28 23:03:50 It seems that there 1 genes have not been annotated by nearestGene mode >> checking seqlevels match... 2023-01-28 23:03:51 >> 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 >> checking seqlevels match... 2023-01-28 23:03:53 >> 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... 2023-01-28 23:03:54 >> checking seqlevels match... 2023-01-28 23:03:55 >> 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... 2023-01-28 23:03:56 Good, your two matrix colnames matchs >> calculating cor and pvalue, which may be time consuming... 2023-01-28 23:03:57 >> merging all info together... 2023-01-28 23:03:58 >> done 2023-01-28 23:03:58 >> checking seqlevels match... 2023-01-28 23:03:58 >> 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 >> using scanPromoter parameter to scan promoter for each gene... 2023-01-28 23:03:58 >> checking seqlevels match... 2023-01-28 23:03:58 >> 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... 2023-01-28 23:03:59 >> there are 85 gene have scaned promoter >> using scanEnhancer parameter to scan Enhancer for each gene... 2023-01-28 23:03:59 >> checking seqlevels match... 2023-01-28 23:03:59 >> 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 >> some scan range may cross Chr bound, trimming... 2023-01-28 23:04:00 >> calculating cor and pvalue, which may be time consuming... 2023-01-28 23:04:01 >> merging all info together... 2023-01-28 23:04:01 >> done 2023-01-28 23:04:01 Good, your two matrix colnames matchs >> calculating cor and pvalue, which may be time consuming... 2023-01-28 23:04:01 >> merging all info together... 2023-01-28 23:04:01 >> done 2023-01-28 23:04:01 >> checking seqlevels match... 2023-01-28 23:04:01 >> 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 ------------ annotatePeak using geneScan mode begins >> preparing gene features information and scan region... 2023-01-28 23:04:01 >> some scan range may cross Chr bound, trimming... 2023-01-28 23:04:02 >> finding overlap peak in gene scan region... 2023-01-28 23:04:02 >> dealing with left peak not your gene scan region... 2023-01-28 23:04:02 >> merging two set peaks... 2023-01-28 23:04:03 >> calculating distance and dealing with gene strand... 2023-01-28 23:04:03 >> merging all info together ... 2023-01-28 23:04:03 >> done 2023-01-28 23:04:03 Good, your two matrix colnames matchs >> calculating cor and pvalue, which may be time consuming... 2023-01-28 23:04:04 >> merging all info together... 2023-01-28 23:04:04 >> done 2023-01-28 23:04:04 >> checking seqlevels match... 2023-01-28 23:04:04 >> 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 >> using scanPromoter parameter to scan promoter for each gene... 2023-01-28 23:04:05 >> checking seqlevels match... 2023-01-28 23:04:05 >> 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... 2023-01-28 23:04:06 >> there are 85 gene have scaned promoter >> using scanEnhancer parameter to scan Enhancer for each gene... 2023-01-28 23:04:06 >> checking seqlevels match... 2023-01-28 23:04:06 >> 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... 2023-01-28 23:04:07 >> calculating cor and pvalue, which may be time consuming... 2023-01-28 23:04:07 >> merging all info together... 2023-01-28 23:04:08 >> done 2023-01-28 23:04:08 Joining, by = "feature_id" Joining, by = "feature_id" `geom_smooth()` using formula = 'y ~ x' Joining, by = "feature_id" Joining, by = "feature_id" `geom_smooth()` using formula = 'y ~ x' [ FAIL 0 | WARN 0 | SKIP 0 | PASS 65 ] > > proc.time() user system elapsed 94.887 1.170 96.314