Back to Multiple platform build/check report for BioC 3.21: simplified long |
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This page was generated on 2025-01-28 11:47 -0500 (Tue, 28 Jan 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" | 4659 |
palomino7 | Windows Server 2022 Datacenter | x64 | R Under development (unstable) (2025-01-21 r87610 ucrt) -- "Unsuffered Consequences" | 4454 |
lconway | macOS 12.7.1 Monterey | x86_64 | R Under development (unstable) (2025-01-22 r87618) -- "Unsuffered Consequences" | 4465 |
kjohnson3 | macOS 13.7.1 Ventura | arm64 | R Under development (unstable) (2025-01-20 r87609) -- "Unsuffered Consequences" | 4419 |
kunpeng2 | Linux (openEuler 22.03 LTS-SP1) | aarch64 | R Under development (unstable) (2024-11-24 r87369) -- "Unsuffered Consequences" | 4409 |
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 824/2286 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||||
GenomicPlot 1.5.2 (landing page) Shuye Pu
| 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 | ![]() | ||||||||
kunpeng2 | Linux (openEuler 22.03 LTS-SP1) / aarch64 | OK | OK | TIMEOUT | ||||||||||
To the developers/maintainers of the GenomicPlot package: - Allow up to 24 hours (and sometimes 48 hours) for your latest push to git@git.bioconductor.org:packages/GenomicPlot.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. - See Martin Grigorov's blog post for how to debug Linux ARM64 related issues on a x86_64 host. |
Package: GenomicPlot |
Version: 1.5.2 |
Command: /home/biocbuild/R/R/bin/R CMD check --install=check:GenomicPlot.install-out.txt --library=/home/biocbuild/R/R/site-library --no-vignettes --timings GenomicPlot_1.5.2.tar.gz |
StartedAt: 2025-01-28 10:56:03 -0000 (Tue, 28 Jan 2025) |
EndedAt: 2025-01-28 11:36:04 -0000 (Tue, 28 Jan 2025) |
EllapsedTime: 2400.9 seconds |
RetCode: None |
Status: TIMEOUT |
CheckDir: GenomicPlot.Rcheck |
Warnings: NA |
############################################################################## ############################################################################## ### ### Running command: ### ### /home/biocbuild/R/R/bin/R CMD check --install=check:GenomicPlot.install-out.txt --library=/home/biocbuild/R/R/site-library --no-vignettes --timings GenomicPlot_1.5.2.tar.gz ### ############################################################################## ############################################################################## * using log directory ‘/home/biocbuild/bbs-3.21-bioc/meat/GenomicPlot.Rcheck’ * using R Under development (unstable) (2024-11-24 r87369) * using platform: aarch64-unknown-linux-gnu * R was compiled by aarch64-unknown-linux-gnu-gcc (GCC) 14.2.0 GNU Fortran (GCC) 14.2.0 * running under: openEuler 24.03 (LTS) * using session charset: UTF-8 * using option ‘--no-vignettes’ * checking for file ‘GenomicPlot/DESCRIPTION’ ... OK * checking extension type ... Package * this is package ‘GenomicPlot’ version ‘1.5.2’ * package encoding: UTF-8 * checking package namespace information ... OK * checking package dependencies ... INFO Imports includes 25 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 ‘GenomicPlot’ can be installed ... WARNING Found the following significant warnings: Warning: program compiled against libxml 212 using older 211 See ‘/home/biocbuild/bbs-3.21-bioc/meat/GenomicPlot.Rcheck/00install.out’ for details. * 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 ...Warning: program compiled against libxml 212 using older 211 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 ... NOTE Warning: program compiled against libxml 212 using older 211 A namespace must be able to be loaded with just the base namespace loaded: otherwise if the namespace gets loaded by a saved object, the session will be unable to start. Probably some imports need to be declared in the NAMESPACE file. * checking whether the namespace can be unloaded cleanly ... OK * checking loading without being on the library search path ... OK * checking dependencies in R code ... NOTE Warning: program compiled against libxml 212 using older 211 * checking S3 generic/method consistency ... WARNING Warning: program compiled against libxml 212 using older 211 See section ‘Generic functions and methods’ in the ‘Writing R Extensions’ manual. * checking replacement functions ... WARNING Warning: program compiled against libxml 212 using older 211 The argument of a replacement function which corresponds to the right hand side must be named ‘value’. * checking foreign function calls ... NOTE Warning: program compiled against libxml 212 using older 211 See chapter ‘System and foreign language interfaces’ in the ‘Writing R Extensions’ manual. * checking R code for possible problems ... NOTE Warning: program compiled against libxml 212 using older 211 get_targeted_genes: no visible binding for global variable ‘5'UTR’ get_targeted_genes: no visible binding for global variable ‘3'UTR’ handle_bam: no visible global function definition for ‘seqlevelsStyle’ handle_bam: no visible global function definition for ‘seqlevelsStyle<-’ handle_bed: no visible global function definition for ‘seqlevelsStyle’ handle_bed: no visible global function definition for ‘seqlevelsStyle<-’ handle_bedGraph: no visible global function definition for ‘seqlevelsStyle’ handle_bedGraph: no visible global function definition for ‘seqlevelsStyle<-’ handle_bw: no visible global function definition for ‘seqlevelsStyle’ handle_bw: no visible global function definition for ‘seqlevelsStyle<-’ plot_bam_correlation: no visible binding for global variable ‘.’ plot_peak_annotation: no visible binding for global variable ‘.’ Undefined global functions or variables: . 3'UTR 5'UTR seqlevelsStyle seqlevelsStyle<- * checking Rd files ... OK * checking Rd metadata ... OK * checking Rd cross-references ... OK * checking for missing documentation entries ... WARNING Warning: program compiled against libxml 212 using older 211 All user-level objects in a package should have documentation entries. See chapter ‘Writing R documentation files’ in the ‘Writing R Extensions’ manual. * checking for code/documentation mismatches ... WARNING Warning: program compiled against libxml 212 using older 211 Warning: program compiled against libxml 212 using older 211 Warning: program compiled against libxml 212 using older 211 * checking Rd \usage sections ... NOTE Warning: program compiled against libxml 212 using older 211 The \usage entries for S3 methods should use the \method markup and not their full name. See chapter ‘Writing R documentation files’ in the ‘Writing R Extensions’ manual. * 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 plot_start_end_with_random 23.247 5.441 27.270 plot_region 19.675 6.986 19.367 plot_locus 18.098 3.697 18.013 plot_5parts_metagene 15.079 6.379 17.781 plot_start_end 15.687 3.360 18.304 plot_locus_with_random 14.409 4.335 15.191 plot_peak_annotation 10.446 0.187 10.655 get_txdb_features 8.962 0.187 9.169 get_targeted_genes 8.709 0.172 8.898 prepare_5parts_genomic_features 6.155 0.036 6.200 * checking for unstated dependencies in ‘tests’ ... OK * checking tests ... Running ‘test-plotFunctions.R’
GenomicPlot.Rcheck/00install.out
############################################################################## ############################################################################## ### ### Running command: ### ### /home/biocbuild/R/R/bin/R CMD INSTALL GenomicPlot ### ############################################################################## ############################################################################## * installing to library ‘/home/biocbuild/R/R-4.5.0-devel_2024-11-24/site-library’ * installing *source* package ‘GenomicPlot’ ... ** using staged installation ** R ** data ** inst ** byte-compile and prepare package for lazy loading Warning: replacing previous import ‘Biostrings::pattern’ by ‘grid::pattern’ when loading ‘genomation’ Warning: program compiled against libxml 212 using older 211 ** help *** installing help indices ** building package indices ** installing vignettes ** testing if installed package can be loaded from temporary location Warning: replacing previous import ‘Biostrings::pattern’ by ‘grid::pattern’ when loading ‘genomation’ Warning: program compiled against libxml 212 using older 211 ** testing if installed package can be loaded from final location Warning: replacing previous import ‘Biostrings::pattern’ by ‘grid::pattern’ when loading ‘genomation’ Warning: program compiled against libxml 212 using older 211 ** testing if installed package keeps a record of temporary installation path * DONE (GenomicPlot)
GenomicPlot.Rcheck/tests/test-plotFunctions.Rout
R Under development (unstable) (2024-11-24 r87369) -- "Unsuffered Consequences" Copyright (C) 2024 The R Foundation for Statistical Computing Platform: aarch64-unknown-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(GenomicPlot) 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 Warning: program compiled against libxml 212 using older 211 Warning message: replacing previous import 'Biostrings::pattern' by 'grid::pattern' when loading 'genomation' > library(testthat) > > Sys.setenv("R_TESTS" = "") > > data(gf5_meta) > data(gf5_genomic) > > gtffile <- system.file("extdata", "gencode.v19.annotation_chr19.gtf", + package = "GenomicPlot") > txdb <- custom_TxDb_from_GTF(gtffile, genome = "hg19") [custom_TxDb_from_GTF] [set_seqinfo] Reading existing granges.rds object from /home/biocbuild/R/R-4.5.0-devel_2024-11-24/site-library/GenomicPlot/extdata/gencode.v19.annotation_chr19.gtf.granges.rds Keeping standard chromosomes only File /home/biocbuild/R/R-4.5.0-devel_2024-11-24/site-library/GenomicPlot/extdata/gencode.v19.annotation_chr19.gtf.granges.rds already exists. Use overwriteObjectAsRds = TRUE to overwrite the file Warning messages: 1: In .get_cds_IDX(mcols0$type, mcols0$phase) : The "phase" metadata column contains non-NA values for features of type stop_codon. This information was ignored. 2: In .makeTxDb_normarg_chrominfo(chrominfo) : genome version information is not available for this TxDb object > > bedQueryFiles <- c( + system.file("extdata", "test_chip_peak_chr19.narrowPeak", + package = "GenomicPlot"), + system.file("extdata", "test_chip_peak_chr19.bed", package = "GenomicPlot"), + system.file("extdata", "test_clip_peak_chr19.bed", package = "GenomicPlot") + ) > names(bedQueryFiles) <- c("NarrowPeak", "SummitPeak", "iCLIPPeak") > > bedImportParams <- setImportParams( + offset = 0, fix_width = 100, fix_point = "center", norm = FALSE, + useScore = FALSE, outRle = TRUE, useSizeFactor = FALSE, genome = "hg19" + ) > > bamQueryFiles <- system.file("extdata", "treat_chr19.bam", + package = "GenomicPlot") > names(bamQueryFiles) <- "clip_bam" > bamInputFiles <- system.file("extdata", "input_chr19.bam", + package = "GenomicPlot") > names(bamInputFiles) <- "clip_input" > > bamImportParams <- setImportParams( + offset = -1, fix_width = 0, fix_point = "start", norm = TRUE, + useScore = FALSE, outRle = TRUE, useSizeFactor = FALSE, genome = "hg19" + ) > > chipQueryFiles <- system.file("extdata", "chip_treat_chr19.bam", + package = "GenomicPlot") > names(chipQueryFiles) <- "chip_bam" > chipInputFiles <- system.file("extdata", "chip_input_chr19.bam", + package = "GenomicPlot") > names(chipInputFiles) <- "chip_input" > > chipImportParams <- setImportParams( + offset = 0, fix_width = 150, fix_point = "start", norm = TRUE, + useScore = FALSE, outRle = TRUE, useSizeFactor = FALSE, genome = "hg19" + ) > > > test_that("testing parallel_countOverlaps", { + importParams <- setImportParams(fix_width = 100, outRle = FALSE) + out_list <- handle_input( + inputFiles = bedQueryFiles, + importParams = importParams, verbose = FALSE, nc = 2 + ) + + chromInfo <- circlize::read.chromInfo(species = "hg19")$df + seqi <- Seqinfo(seqnames = chromInfo$chr, seqlengths = chromInfo$end, + isCircular = rep(FALSE, nrow(chromInfo)), + genome = "hg19") + grange_list <- lapply(out_list, function(x) x$query) + tilewidth <- 100000 + tileBins <- tileGenome(seqi, tilewidth = tilewidth, + cut.last.tile.in.chrom = TRUE) + + score_list1 <- parallel_countOverlaps(grange_list, tileBins, nc = 2) + }) ── Skip: testing parallel_countOverlaps ──────────────────────────────────────── Reason: empty test > > test_that("testing parallel_scoreMatrixBin", { + + queryRegion <- handle_input(chipQueryFiles, chipImportParams, + verbose = TRUE)[[1]]$query + + importParams <- setImportParams(outRle = FALSE) + + windowRegion <- handle_bed(bedQueryFiles[1], importParams, verbose = TRUE)$query + + out <- parallel_scoreMatrixBin( + queryRegions = queryRegion, + windowRs = windowRegion, + bin_num = 50, + bin_op = "mean", + weight_col = "score", + stranded = TRUE, + nc = 2 + ) + }) ── Skip: testing parallel_scoreMatrixBin ─────────────────────────────────────── Reason: empty test > > test_that("testing handle_bed", { + out <- handle_bed(bedQueryFiles[1], bedImportParams, verbose = TRUE) + }) ── Skip: testing handle_bed ──────────────────────────────────────────────────── Reason: empty test > > test_that("testing effective_size", { + importParams <- setImportParams(outRle = FALSE) + out_list <- handle_input( + inputFiles = c(chipQueryFiles, chipInputFiles), + importParams = importParams, verbose = TRUE, nc = 2 + ) + + out <- effective_size(out_list, outRle = TRUE) + }) ── Skip: testing effective_size ──────────────────────────────────────────────── Reason: empty test > > test_that("testing handle_input", { + + queryFiles2 <- system.file("extdata", "test_wig_chr19_+.wig", + package = "GenomicPlot") + names(queryFiles2) <- "test_wig" + + queryFiles3 <- system.file("extdata", "test_wig_chr19_+.bw", + package = "GenomicPlot") + names(queryFiles3) <- "test_bw" + + importParams <- setImportParams() + + out <- handle_input(c(bamQueryFiles, queryFiles2, queryFiles3), + importParams, verbose = TRUE) + }) ── Skip: testing handle_input ────────────────────────────────────────────────── Reason: empty test > > test_that("testing plot_bam_correlation", { + + importParams <- setImportParams(fix_width = 150, outRle = FALSE) + + plot_bam_correlation( + bamFiles = c(chipQueryFiles, chipInputFiles), binSize = 100000, + outPrefix = NULL, importParams = importParams, nc = 2, verbose = FALSE + ) + }) ── Skip: testing plot_bam_correlation ────────────────────────────────────────── Reason: empty test > > test_that("testing plot_overlap_bed", { + importParams <- setImportParams(fix_width = 100, outRle = FALSE) + plot_overlap_bed( + bedList = bedQueryFiles, importParams = importParams, pairOnly = FALSE, + stranded = FALSE, outPrefix = NULL + ) + }) ── Skip: testing plot_overlap_bed ────────────────────────────────────────────── Reason: empty test > > test_that("testing plot_argument_list", { + + alist <- list( + "txdb" = txdb, "treat" = bamQueryFiles, "control" = bamInputFiles, + "feature" = gf5_meta, "param" = bamImportParams + ) + + p <- GenomicPlot:::plot_named_list(alist) + }) ── Skip: testing plot_argument_list ──────────────────────────────────────────── Reason: empty test > > > test_that("testing plot_peak_annotation", { + plot_peak_annotation( + peakFile = bedQueryFiles[2], gtfFile = gtffile, importParams = bedImportParams, + fiveP = -2000, dsTSS = 200, threeP = 2000, simple = FALSE + ) + }) ── Warning: testing plot_peak_annotation ─────────────────────────────────────── The "phase" metadata column contains non-NA values for features of type stop_codon. This information was ignored. Backtrace: ▆ 1. └─GenomicPlot::plot_peak_annotation(...) 2. └─txdbmaker::makeTxDbFromGRanges(gff) 3. └─txdbmaker:::.get_cds_IDX(mcols0$type, mcols0$phase) ── Warning: testing plot_peak_annotation ─────────────────────────────────────── genome version information is not available for this TxDb object Backtrace: ▆ 1. └─GenomicPlot::plot_peak_annotation(...) 2. └─txdbmaker::makeTxDbFromGRanges(gff) 3. └─txdbmaker::makeTxDb(...) 4. └─txdbmaker:::.makeTxDb_normarg_chrominfo(chrominfo) ── Skip: testing plot_peak_annotation ────────────────────────────────────────── Reason: empty test > > > test_that("testing plot_overlap_genes", { + testfile1 <- system.file("extdata", "test_file1.txt", + package = "GenomicPlot") + testfile2 <- system.file("extdata", "test_file2.txt", + package = "GenomicPlot") + testfile3 <- system.file("extdata", "test_file3.txt", + package = "GenomicPlot") + testfile4 <- system.file("extdata", "test_file4.txt", + package = "GenomicPlot") + testfiles <- c(testfile1, testfile2, testfile3, testfile4) + names(testfiles) <- c("test1", "test2", "test3", "test4") + + plot_overlap_genes(testfiles, c(3,2,1,1), pairOnly = FALSE) + }) ── Skip: testing plot_overlap_genes ──────────────────────────────────────────── Reason: empty test > > test_that("testing plot_5parts_metagene", { + plot_5parts_metagene( + queryFiles = bedQueryFiles, + gFeatures_list = list("metagene" = gf5_meta), + inputFiles = NULL, + importParams = bedImportParams, + verbose = FALSE, + smooth = TRUE, + scale = FALSE, + stranded = TRUE, + outPrefix = NULL, + transform = NA, + heatmap = TRUE, + rmOutlier = 0, + heatRange = NULL, + nc = 2 + ) + })
GenomicPlot.Rcheck/GenomicPlot-Ex.timings
name | user | system | elapsed | |
aov_TukeyHSD | 0.019 | 0.000 | 0.019 | |
check_constraints | 0.194 | 0.012 | 0.734 | |
custom_TxDb_from_GTF | 1.241 | 0.107 | 1.353 | |
draw_boxplot_by_factor | 0.556 | 0.052 | 0.612 | |
draw_boxplot_wo_outlier | 0.254 | 0.020 | 0.275 | |
draw_combo_plot | 2.181 | 0.244 | 2.430 | |
draw_locus_profile | 0.468 | 0.028 | 0.498 | |
draw_matrix_heatmap | 1.594 | 0.135 | 1.733 | |
draw_mean_se_barplot | 0.524 | 0.021 | 0.546 | |
draw_quantile_plot | 0.619 | 0.039 | 0.660 | |
draw_rank_plot | 0.575 | 0.048 | 0.623 | |
draw_region_landmark | 0.013 | 0.000 | 0.012 | |
draw_region_name | 0.008 | 0.000 | 0.008 | |
draw_region_profile | 0.347 | 0.004 | 0.352 | |
draw_stacked_profile | 2.198 | 0.148 | 2.351 | |
effective_size | 0.687 | 0.300 | 0.938 | |
extract_longest_tx | 1.661 | 0.252 | 1.918 | |
filter_by_nonoverlaps_stranded | 0.416 | 0.000 | 0.417 | |
filter_by_overlaps_nonstranded | 1.364 | 0.315 | 1.682 | |
filter_by_overlaps_stranded | 0.296 | 0.010 | 0.307 | |
find_mate | 0.003 | 0.000 | 0.002 | |
gene2tx | 0.321 | 0.008 | 0.332 | |
get_genomic_feature_coordinates | 2.164 | 0.056 | 2.224 | |
get_targeted_genes | 8.709 | 0.172 | 8.898 | |
get_txdb_features | 8.962 | 0.187 | 9.169 | |
gr2df | 0.038 | 0.000 | 0.037 | |
handle_bam | 0.171 | 0.004 | 0.178 | |
handle_bed | 0.128 | 0.000 | 0.129 | |
handle_bedGraph | 0.077 | 0.000 | 0.077 | |
handle_bw | 0.345 | 0.012 | 0.361 | |
handle_input | 1.512 | 0.024 | 1.547 | |
handle_wig | 0.279 | 0.000 | 0.280 | |
impute_hm | 0.007 | 0.000 | 0.006 | |
inspect_matrix | 0.015 | 0.000 | 0.015 | |
make_subTxDb_from_GTF | 0.824 | 0.004 | 0.829 | |
overlap_pair | 0.379 | 0.008 | 0.388 | |
overlap_quad | 3.683 | 0.060 | 3.750 | |
overlap_triple | 1.190 | 0.072 | 1.265 | |
parallel_countOverlaps | 0.502 | 0.285 | 0.722 | |
parallel_scoreMatrixBin | 0.641 | 0.435 | 1.021 | |
plot_5parts_metagene | 15.079 | 6.379 | 17.781 | |
plot_bam_correlation | 1.266 | 0.462 | 1.670 | |
plot_locus | 18.098 | 3.697 | 18.013 | |
plot_locus_with_random | 14.409 | 4.335 | 15.191 | |
plot_named_list | 1.001 | 0.171 | 1.175 | |
plot_overlap_bed | 1.669 | 0.056 | 1.728 | |
plot_overlap_genes | 1.263 | 0.063 | 1.330 | |
plot_peak_annotation | 10.446 | 0.187 | 10.655 | |
plot_region | 19.675 | 6.986 | 19.367 | |
plot_start_end | 15.687 | 3.360 | 18.304 | |
plot_start_end_with_random | 23.247 | 5.441 | 27.270 | |
prepare_3parts_genomic_features | 1.818 | 0.048 | 1.868 | |
prepare_5parts_genomic_features | 6.155 | 0.036 | 6.200 | |
process_scoreMatrix | 0.021 | 0.003 | 0.024 | |
rank_rows | 0.011 | 0.000 | 0.010 | |
ratio_over_input | 0.001 | 0.000 | 0.001 | |
rm_outlier | 0.005 | 0.000 | 0.004 | |
setImportParams | 0.001 | 0.000 | 0.000 | |
set_seqinfo | 0.004 | 0.000 | 0.004 | |
start_parallel | 0.008 | 0.200 | 0.151 | |
stop_parallel | 0.011 | 0.188 | 0.141 | |