Back to Multiple platform build/check report for BioC 3.14 |
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This page was generated on 2022-04-13 12:07:09 -0400 (Wed, 13 Apr 2022).
Hostname | OS | Arch (*) | R version | Installed pkgs |
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nebbiolo2 | Linux (Ubuntu 20.04.4 LTS) | x86_64 | 4.1.3 (2022-03-10) -- "One Push-Up" | 4324 |
tokay2 | Windows Server 2012 R2 Standard | x64 | 4.1.3 (2022-03-10) -- "One Push-Up" | 4077 |
machv2 | macOS 10.14.6 Mojave | x86_64 | 4.1.3 (2022-03-10) -- "One Push-Up" | 4137 |
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 |
To the developers/maintainers of the QDNAseq package: - Please allow up to 24 hours (and sometimes 48 hours) for your latest push to git@git.bioconductor.org:packages/QDNAseq.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 1496/2083 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||||
QDNAseq 1.30.0 (landing page) Daoud Sie
| nebbiolo2 | Linux (Ubuntu 20.04.4 LTS) / x86_64 | OK | OK | OK | |||||||||
tokay2 | Windows Server 2012 R2 Standard / x64 | OK | OK | OK | OK | |||||||||
machv2 | macOS 10.14.6 Mojave / x86_64 | OK | OK | OK | OK | |||||||||
Package: QDNAseq |
Version: 1.30.0 |
Command: C:\Users\biocbuild\bbs-3.14-bioc\R\bin\R.exe CMD check --force-multiarch --install=check:QDNAseq.install-out.txt --library=C:\Users\biocbuild\bbs-3.14-bioc\R\library --no-vignettes --timings QDNAseq_1.30.0.tar.gz |
StartedAt: 2022-04-13 01:03:39 -0400 (Wed, 13 Apr 2022) |
EndedAt: 2022-04-13 01:17:59 -0400 (Wed, 13 Apr 2022) |
EllapsedTime: 859.7 seconds |
RetCode: 0 |
Status: OK |
CheckDir: QDNAseq.Rcheck |
Warnings: 0 |
############################################################################## ############################################################################## ### ### Running command: ### ### C:\Users\biocbuild\bbs-3.14-bioc\R\bin\R.exe CMD check --force-multiarch --install=check:QDNAseq.install-out.txt --library=C:\Users\biocbuild\bbs-3.14-bioc\R\library --no-vignettes --timings QDNAseq_1.30.0.tar.gz ### ############################################################################## ############################################################################## * using log directory 'C:/Users/biocbuild/bbs-3.14-bioc/meat/QDNAseq.Rcheck' * using R version 4.1.3 (2022-03-10) * using platform: x86_64-w64-mingw32 (64-bit) * using session charset: ISO8859-1 * using option '--no-vignettes' * checking for file 'QDNAseq/DESCRIPTION' ... OK * this is package 'QDNAseq' version '1.30.0' * 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 whether package 'QDNAseq' 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 * loading checks for arch 'i386' ** 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 * loading checks for arch 'x64' ** 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 ... ** running examples for arch 'i386' ... OK Examples with CPU (user + system) or elapsed time > 5s user system elapsed frequencyPlot 24.31 0.03 24.34 callBins 24.02 0.21 24.23 normalizeSegmentedBins 15.22 0.00 15.22 segmentBins 15.10 0.00 15.09 ** running examples for arch 'x64' ... OK Examples with CPU (user + system) or elapsed time > 5s user system elapsed callBins 19.80 0.17 19.97 frequencyPlot 19.41 0.06 19.47 normalizeSegmentedBins 8.41 0.00 8.40 segmentBins 7.97 0.00 7.97 * checking for unstated dependencies in 'tests' ... OK * checking tests ... ** running tests for arch 'i386' ... Running 'QDNAseq,copyneutral.R' Running 'QDNAseq,gain-copyneutral-gain.R' Running 'QDNAseq,parallel-reproducibility.R' Running 'QDNAseq.R' Running 'binReadCounts.R' OK ** running tests for arch 'x64' ... Running 'QDNAseq,copyneutral.R' Running 'QDNAseq,gain-copyneutral-gain.R' Running 'QDNAseq,parallel-reproducibility.R' Running 'QDNAseq.R' Running 'binReadCounts.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
QDNAseq.Rcheck/00install.out
############################################################################## ############################################################################## ### ### Running command: ### ### C:\cygwin\bin\curl.exe -O http://155.52.207.166/BBS/3.14/bioc/src/contrib/QDNAseq_1.30.0.tar.gz && rm -rf QDNAseq.buildbin-libdir && mkdir QDNAseq.buildbin-libdir && C:\Users\biocbuild\bbs-3.14-bioc\R\bin\R.exe CMD INSTALL --merge-multiarch --build --library=QDNAseq.buildbin-libdir QDNAseq_1.30.0.tar.gz && C:\Users\biocbuild\bbs-3.14-bioc\R\bin\R.exe CMD INSTALL QDNAseq_1.30.0.zip && rm QDNAseq_1.30.0.tar.gz QDNAseq_1.30.0.zip ### ############################################################################## ############################################################################## % Total % Received % Xferd Average Speed Time Time Time Current Dload Upload Total Spent Left Speed 0 0 0 0 0 0 0 0 --:--:-- --:--:-- --:--:-- 0 100 585k 100 585k 0 0 1411k 0 --:--:-- --:--:-- --:--:-- 1413k install for i386 * installing *source* package 'QDNAseq' ... ** using staged installation ** R ** data ** inst ** byte-compile and prepare package for lazy loading ** help *** installing help indices converting help for package 'QDNAseq' finding HTML links ... done LGG150 html QDNAseq-defunct html QDNAseq-package html QDNAseqCopyNumbers html QDNAseqReadCounts html QDNAseqSignals html addPhenodata html applyFilters html binReadCounts html callBins html compareToReference html correctBins html createBins html estimateCorrection html exportBins html finding level-2 HTML links ... done frequencyPlot html getBinAnnotations html highlightFilters html isobarPlot html makeCgh html noisePlot html normalizeBins html normalizeSegmentedBins html plot html poolRuns html segmentBins html smoothOutlierBins html ** 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 install for x64 * installing *source* package 'QDNAseq' ... ** testing if installed package can be loaded * MD5 sums packaged installation of 'QDNAseq' as QDNAseq_1.30.0.zip * DONE (QDNAseq) * installing to library 'C:/Users/biocbuild/bbs-3.14-bioc/R/library' package 'QDNAseq' successfully unpacked and MD5 sums checked
QDNAseq.Rcheck/tests_i386/binReadCounts.Rout R version 4.1.3 (2022-03-10) -- "One Push-Up" Copyright (C) 2022 The R Foundation for Statistical Computing Platform: i386-w64-mingw32/i386 (32-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(QDNAseq) > > if (requireNamespace("QDNAseq.hg19", quietly = TRUE)) { + bins <- getBinAnnotations(500, genome = "hg19") + print(bins) + + bam <- system.file("extdata", "ex1.bam", package = "Rsamtools") + print(bam) + + counts <- binReadCounts(bins, bamfiles = bam) + print(counts) + + ## BUG: https://github.com/ccagc/QDNAseq/issues/89 + counts2 <- binReadCounts(bins, bamfiles = bam, chunkSize = 10e3) + print(counts2) + } Loaded bin annotations for genome 'hg19', bin size 500 kbp, and experiment type 'SR50' from annotation package QDNAseq.hg19 v1.24.0 QDNAseq bin annotations for Hsapiens, build hg19. Created by Ilari Scheinin with QDNAseq 0.7.5, 2014-02-06 09:20:46. An object of class 'AnnotatedDataFrame' rowNames: 1:1-500000 1:500001-1000000 ... Y:59000001-59373566 (6206 total) varLabels: chromosome start ... use (9 total) varMetadata: labelDescription [1] "C:/Users/biocbuild/bbs-3.14-bioc/R/library/Rsamtools/extdata/ex1.bam" ex1 (1 of 1): extracting reads ... binning ... QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 6206 features, 1 samples element names: counts protocolData: none phenoData sampleNames: ex1 varLabels: name total.reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 1:1-500000 1:500001-1000000 ... Y:59000001-59373566 (6206 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: ex1 (1 of 1): extracting reads ... binning chunk - seq1:1:10001 binning chunk - seq2:1:10001 QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 6206 features, 1 samples element names: counts protocolData: none phenoData sampleNames: ex1 varLabels: name total.reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 1:1-500000 1:500001-1000000 ... Y:59000001-59373566 (6206 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > > > proc.time() user system elapsed 6.01 0.39 6.43 |
QDNAseq.Rcheck/tests_x64/binReadCounts.Rout R version 4.1.3 (2022-03-10) -- "One Push-Up" Copyright (C) 2022 The R Foundation for Statistical Computing Platform: x86_64-w64-mingw32/x64 (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(QDNAseq) > > if (requireNamespace("QDNAseq.hg19", quietly = TRUE)) { + bins <- getBinAnnotations(500, genome = "hg19") + print(bins) + + bam <- system.file("extdata", "ex1.bam", package = "Rsamtools") + print(bam) + + counts <- binReadCounts(bins, bamfiles = bam) + print(counts) + + ## BUG: https://github.com/ccagc/QDNAseq/issues/89 + counts2 <- binReadCounts(bins, bamfiles = bam, chunkSize = 10e3) + print(counts2) + } Loaded bin annotations for genome 'hg19', bin size 500 kbp, and experiment type 'SR50' from annotation package QDNAseq.hg19 v1.24.0 QDNAseq bin annotations for Hsapiens, build hg19. Created by Ilari Scheinin with QDNAseq 0.7.5, 2014-02-06 09:20:46. An object of class 'AnnotatedDataFrame' rowNames: 1:1-500000 1:500001-1000000 ... Y:59000001-59373566 (6206 total) varLabels: chromosome start ... use (9 total) varMetadata: labelDescription [1] "C:/Users/biocbuild/bbs-3.14-bioc/R/library/Rsamtools/extdata/ex1.bam" ex1 (1 of 1): extracting reads ... binning ... QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 6206 features, 1 samples element names: counts protocolData: none phenoData sampleNames: ex1 varLabels: name total.reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 1:1-500000 1:500001-1000000 ... Y:59000001-59373566 (6206 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: ex1 (1 of 1): extracting reads ... binning chunk - seq1:1:10001 binning chunk - seq2:1:10001 QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 6206 features, 1 samples element names: counts protocolData: none phenoData sampleNames: ex1 varLabels: name total.reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 1:1-500000 1:500001-1000000 ... Y:59000001-59373566 (6206 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > > > proc.time() user system elapsed 9.06 0.34 11.42 |
QDNAseq.Rcheck/tests_i386/QDNAseq.Rout R version 4.1.3 (2022-03-10) -- "One Push-Up" Copyright (C) 2022 The R Foundation for Statistical Computing Platform: i386-w64-mingw32/i386 (32-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(QDNAseq) > library(Biobase) ## combine(), sampleNames() 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, 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 Welcome to Bioconductor Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation("Biobase")', and for packages 'citation("pkgname")'. > library(utils) > > # Load data > data(LGG150) > data <- LGG150 > print(data) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > stopifnot(inherits(data, "QDNAseqReadCounts")) > > # Plot isobars of read counts > isobarPlot(data) Plotting sample LGG150 median read counts > > # Plot copy number profile > plot(data, ylim=c(-100, 200)) Plotting sample LGG150 (1 of 1) ... > highlightFilters(data, residual=TRUE, blacklist=TRUE) Highlighted 3,375 bins. > > # Filter out "bad" bins > dataF <- applyFilters(data, residual=TRUE, blacklist=TRUE) 38,819 total bins 38,819 of which in selected chromosomes 36,722 of which with reference sequence 33,347 final bins > print(dataF) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > plot(dataF, ylim=c(-100, 200)) Plotting sample LGG150 (1 of 1) ... > stopifnot(inherits(dataF, "QDNAseqReadCounts")) > > # Correct read counts as a function of GC content and mappability > dataC <- correctBins(dataF) Calculating correction for GC content and mappability Calculating fit for sample LGG150 (1 of 1) ... Done. > print(dataC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > plot(dataC, ylim=c(-100, 200)) Plotting sample LGG150 (1 of 1) ... > stopifnot(inherits(dataC, "QDNAseqCopyNumbers")) > > # Normalize binned read counts to have diploid normal copy number > dataN <- normalizeBins(dataC) Applying median normalization ... > print(dataN) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > plot(dataN) Plotting sample LGG150 (1 of 1) ... > stopifnot(inherits(dataN, "QDNAseqCopyNumbers")) > > # Plot noise > noisePlot(dataF) Calculating correction for GC content and mappability Calculating fit for sample LGG150 (1 of 1) ... Done. > > # Segment copy numbers > fit <- segmentBins(dataN) Performing segmentation: Segmenting: LGG150 (1 of 1) ... > print(fit) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > plot(fit) Plotting sample LGG150 (1 of 1) ... > stopifnot(inherits(fit, "QDNAseqCopyNumbers")) > > # Call copy-number segments > fitC <- callBins(fit) EM algorithm started ... [1] "Total number of segments present in the data: 10" [1] "Number of segments used for fitting the model: 9" 39066975515645119.342.1801238012255594244.693.6801238010146328244.677.5 Calling iteration1: optim results time: 0 minimum: 16445.6418287481 116443.1634295677-0.939948404909672-0.5351158716347190.04999922851584940.1357341814220170.2320391157632851.492692224927890.46336036623653-0.000744748796554230.0111894143724591-0.000962583906213420.3145629342085070.798554843389167 39082025517992119.342.1801238012255594244.693.6801238010146328244.677.5 Calling iteration2: optim results time: 0 minimum: 16445.5781374328 116443.1331012469-0.932876677515091-0.5359433038809970.0499979048415910.1114729434735370.1905642555481931.861013902305770.4314700360573740.0001440687684073730.01118427659401560.0007568920162792620.2061088124299370.874022351578009 39082025517992119.342.1801238012255594244.693.6801238010146328244.677.5 Calling iteration3: optim results time: 0 minimum: 16445.5975371627 116443.1273697069-0.924012853099608-0.5365177469718940.04999923288882760.108573194240180.1856071014916831.753751992204390.4694950401327692.93313204138107e-050.0111878614439676-0.0001759851682342870.07360543573369820.943675664015282 EM algorithm done ... Computing posterior probabilities for all segments ... Total time:0minutes Adjusting segmented data for cellularity ... Cellularity sample1: 1 Adjusting normalized data for cellularity ... Cellularity sample1: 1 1 39108705720821119.443.7801238012255594244.693.6801238010146328244.677.5 39108895887565119.445801238012255594244.693.6801238010146328244.677.5 39108865887561119.445801238012255594244.693.6801238010146328244.677.5 39109146154576119.447801238012255594244.693.6801238010146328244.677.5 39113416155214119.447801238012255594244.693.6801238010146328244.677.5 39113506155217119.447801238012255594244.693.6801238010146328244.677.5 39113596155220119.447801238012255594244.693.6801238010146328244.677.5 39113686155223119.447801238012255594244.693.6801238010146328244.677.5 39113776155226119.447801238012255594244.693.6801238010146328244.677.5 39113836155228119.447801238012255594244.693.6801238010146328244.677.5 39114026221942119.447.5801238012255594244.693.6801238010146328244.677.5 39118196222179119.447.5801238012255594244.693.6801238010146328244.677.5 FINISHED! Total time:0minutes There were 50 or more warnings (use warnings() to see the first 50) > print(fitC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: calls, copynumber, probamp, probdloss, probgain, probloss, probnorm, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > plot(fitC) Plotting sample LGG150 (1 of 1) ... > > > # --------------------------------------------------------------- > # Exporting > # --------------------------------------------------------------- > message("* exportBins() ...") * exportBins() ... > > sets <- list(data = data, dataC = dataC, fit = fit, fitC = fitC) > for (name in names(sets)) { + set <- sets[[name]] + formats <- c("tsv", "igv", "bed") + if (name == "fitC") formats <- c(formats, "vcf", "seg") + for (format in formats) { + types <- c("copynumber") + if (name %in% c("fit", "fitC")) types <- c(types, "segments") + if (name == "fitC") types <- c(types, "calls") + for (type in types) { + fileext <- sprintf(".%s.%s", type, format) + templates <- c("QDNAseq-%s.", "QDNAseq-%i.", "QDNAseq-%03i.") + if (ncol(set) == 1L || !(format %in% c("bed", "seg", "vcf"))) { + templates <- c("QDNAseq.", templates) + } + for (template in templates) { + file <- tempfile(pattern = template, fileext = fileext) + message(sprintf(" - exportBins(<%d samples>, format=\"%s\", type=\"%s\", file=\"%s\")", ncol(set), format, type, template)) + file <- exportBins(set, file = file, format = format, type = type) + message(sprintf(" File(s) written: [n=%d] %s", + length(file), paste(sQuote(file), collapse = ", "))) + stopifnot(all(file_test("-f", file))) + file.remove(file) + stopifnot(!any(file_test("-f", file))) + } + } + } + } - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac011473b87.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac093577b.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac0352f36f1.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac05ec7391.copynumber.tsv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac09ce5508.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac05406574e.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac03f2c7423.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac0206a5166.copynumber.igv' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac08864334.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac0523d57f0.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac030a415a8.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac025957b6a.copynumber.bed' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac048672e8e.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac047853afe.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac023a246fc.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac059945e03.copynumber.tsv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac0182a53ae.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac0496e6c7.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac033314df1.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac050da628c.copynumber.igv' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac058cf3bf.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac031ec1ad0.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac01e2332c.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac037c6bd2.copynumber.bed' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac0c187501.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac021d7451.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac0504a3aa6.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac017b31297.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac0730c6345.segments.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac0136922b6.segments.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac023822c2c.segments.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac03c5e3212.segments.tsv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac03c7573.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac07cc21c1f.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac07ba56bdf.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac0137e446c.copynumber.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac043613507.segments.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac026721e1.segments.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac01a5662b5.segments.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac02cb8f45.segments.igv' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac05da5308f.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac039bf502.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac0593836f7.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac0fd6202d.copynumber.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac03a554a2f.segments.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac07b951ac1.segments.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac0107354c1.segments.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac05746192b.segments.bed' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac0504d311e.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac04699710c.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac0d364685.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac05a9a4d3a.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac05cac6d26.segments.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac031df5308.segments.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac0182f5d88.segments.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac069062cc7.segments.tsv' - exportBins(<1 samples>, format="tsv", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac071542f28.calls.tsv' - exportBins(<1 samples>, format="tsv", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac06f5f1d8c.calls.tsv' - exportBins(<1 samples>, format="tsv", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac0c152a63.calls.tsv' - exportBins(<1 samples>, format="tsv", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac013e5234.calls.tsv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac0136b7195.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac05e7363a6.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac07c1f4583.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac09347e58.copynumber.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac069dc68f6.segments.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq-%s.") 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File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac04dc8ab5.copynumber.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac037757bbf.segments.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac07e6971ed.segments.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac07c2b5739.segments.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac0551040a0.segments.bed' - exportBins(<1 samples>, format="bed", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac0634a3f44.calls.bed' - exportBins(<1 samples>, format="bed", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac01f713c2.calls.bed' - exportBins(<1 samples>, format="bed", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac01a492d14.calls.bed' - exportBins(<1 samples>, format="bed", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac079d927bd.calls.bed' - exportBins(<1 samples>, format="vcf", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac03c0b670c.copynumber.vcf' - exportBins(<1 samples>, format="vcf", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac0536751b8.copynumber.vcf' - exportBins(<1 samples>, format="vcf", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac016b34427.copynumber.vcf' - exportBins(<1 samples>, format="vcf", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac02785e19.copynumber.vcf' - exportBins(<1 samples>, format="vcf", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac03b93e96.segments.vcf' - exportBins(<1 samples>, format="vcf", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac07d632848.segments.vcf' - exportBins(<1 samples>, format="vcf", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac063e19ab.segments.vcf' - exportBins(<1 samples>, format="vcf", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac0b677fb6.segments.vcf' - exportBins(<1 samples>, format="vcf", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac0239c1ef5.calls.vcf' - exportBins(<1 samples>, format="vcf", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac01e16e1f.calls.vcf' - exportBins(<1 samples>, format="vcf", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac02a4236ad.calls.vcf' - exportBins(<1 samples>, format="vcf", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac061c2330c.calls.vcf' - exportBins(<1 samples>, format="seg", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac05abf5f50.copynumber.seg' - exportBins(<1 samples>, format="seg", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac06941189b.copynumber.seg' - exportBins(<1 samples>, format="seg", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac0271c488e.copynumber.seg' - exportBins(<1 samples>, format="seg", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac06dcd582.copynumber.seg' - exportBins(<1 samples>, format="seg", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac07c6f1563.segments.seg' - exportBins(<1 samples>, format="seg", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac012467052.segments.seg' - exportBins(<1 samples>, format="seg", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac04aad984.segments.seg' - exportBins(<1 samples>, format="seg", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac02d6c17f9.segments.seg' - exportBins(<1 samples>, format="seg", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac03ec025fc.calls.seg' - exportBins(<1 samples>, format="seg", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150.3ac07498258b.calls.seg' - exportBins(<1 samples>, format="seg", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac062d97917.calls.seg' - exportBins(<1 samples>, format="seg", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac03eaa1b42.calls.seg' > > sets <- list(data = data, dataC = dataC, fit = fit, fitC = fitC) > sets <- lapply(sets, FUN = function(set) { + stopifnot(ncol(set) == 1L) + name <- sampleNames(set) + setA <- set + sampleNames(setA) <- sprintf("%sa", name) + setB <- set + sampleNames(setB) <- sprintf("%sb", name) + combine(setA, setB) + }) > > for (name in names(sets)) { + set <- sets[[name]] + stopifnot(ncol(set) == 2L) + formats <- c("tsv", "igv", "bed") + if (name == "fitC") formats <- c(formats, "vcf", "seg") + for (format in formats) { + types <- c("copynumber") + if (name %in% c("fit", "fitC")) types <- c(types, "segments") + if (name == "fitC") types <- c(types, "calls") + for (type in types) { + fileext <- sprintf(".%s.%s", type, format) + templates <- c("QDNAseq-%s.", "QDNAseq-%i.", "QDNAseq-%03i.") + if (ncol(set) == 1L || !(format %in% c("bed", "seg", "vcf"))) { + templates <- c("QDNAseq.", templates) + } + for (template in templates) { + file <- tempfile(pattern = template, fileext = fileext) + message(sprintf(" - exportBins(<%d samples>, format=\"%s\", type=\"%s\", file=\"%s\")", ncol(set), format, type, template)) + file <- exportBins(set, file = file, format = format, type = type) + message(sprintf(" File(s) written: [n=%d] %s", + length(file), paste(sQuote(file), collapse = ", "))) + stopifnot(all(file_test("-f", file))) + file.remove(file) + stopifnot(!any(file_test("-f", file))) + } + } + } + } - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac01908257f.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac0734234c3.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac0240a64a5.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac07a331ca2.copynumber.tsv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac03262862.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac03f341b29.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac01fab3fdf.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac01dd92255.copynumber.igv' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac0602c23b2.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac0602c23b2.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac049c25b22.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac049c25b22.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac04aad4d49.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac04aad4d49.copynumber.bed' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac07131808.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac034897d8c.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac0472350c6.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac0140516be.copynumber.tsv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac07d79b5e.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac01ce06da4.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac040f45661.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac0b2b35ea.copynumber.igv' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac0d49386c.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac0d49386c.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac0105bdc2.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac0105bdc2.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac038b338f3.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac038b338f3.copynumber.bed' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac0169d6cce.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac071e5663d.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac04e697a40.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac05a447cb0.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac03a5ae40.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac01053134f.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac02d3d628e.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac03e6e7181.segments.tsv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac06e683668.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac01bc7214.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac0784d69ae.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac03d5f1781.copynumber.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac054e5344.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac02ded3572.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac05ed356b8.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac051245381.segments.igv' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac0229a7d24.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac0229a7d24.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac075d92d43.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac075d92d43.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac0724f1556.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac0724f1556.copynumber.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac08327385.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac08327385.segments.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac0415d1f2f.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac0415d1f2f.segments.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac06e1532d5.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac06e1532d5.segments.bed' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac03503649.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac07e0345.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac04aaa6fdc.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac0295b656b.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac038761fe3.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac01eeb70ac.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac03c1b397a.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac0130836bb.segments.tsv' - exportBins(<2 samples>, format="tsv", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac04bf25e8b.calls.tsv' - exportBins(<2 samples>, format="tsv", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac067f05c.calls.tsv' - exportBins(<2 samples>, format="tsv", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac05e4c72a9.calls.tsv' - exportBins(<2 samples>, format="tsv", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac0599d476e.calls.tsv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac03b0653c.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac07bf51228.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac0b5d26df.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac0694213a3.copynumber.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac01c042e06.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac034e13598.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac05742ee4.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac0763e6f6c.segments.igv' - exportBins(<2 samples>, format="igv", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq.3ac02e842a8c.calls.igv' - exportBins(<2 samples>, format="igv", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%s.3ac00e69.calls.igv' - exportBins(<2 samples>, format="igv", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%i.3ac05d393956.calls.igv' - exportBins(<2 samples>, format="igv", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-%03i.3ac01780534f.calls.igv' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac049df3484.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac049df3484.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac0408090b.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac0408090b.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac068582325.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac068582325.copynumber.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac0711a78c6.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac0711a78c6.segments.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac05bb56e3a.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac05bb56e3a.segments.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac041f65f21.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac041f65f21.segments.bed' - exportBins(<2 samples>, format="bed", type="calls", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac048032018.calls.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac048032018.calls.bed' - exportBins(<2 samples>, format="bed", type="calls", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac06ec046bf.calls.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac06ec046bf.calls.bed' - exportBins(<2 samples>, format="bed", type="calls", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac07667330d.calls.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac07667330d.calls.bed' - exportBins(<2 samples>, format="vcf", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac03ad96c05.copynumber.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac03ad96c05.copynumber.vcf' - exportBins(<2 samples>, format="vcf", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac07f6e3346.copynumber.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac07f6e3346.copynumber.vcf' - exportBins(<2 samples>, format="vcf", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac0e4de1d.copynumber.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac0e4de1d.copynumber.vcf' - exportBins(<2 samples>, format="vcf", type="segments", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac06f9e37f0.segments.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac06f9e37f0.segments.vcf' - exportBins(<2 samples>, format="vcf", type="segments", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac05f065141.segments.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac05f065141.segments.vcf' - exportBins(<2 samples>, format="vcf", type="segments", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac01a51779e.segments.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac01a51779e.segments.vcf' - exportBins(<2 samples>, format="vcf", type="calls", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac03a3f1636.calls.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac03a3f1636.calls.vcf' - exportBins(<2 samples>, format="vcf", type="calls", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac0ec37beb.calls.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac0ec37beb.calls.vcf' - exportBins(<2 samples>, format="vcf", type="calls", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac023b6b16.calls.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac023b6b16.calls.vcf' - exportBins(<2 samples>, format="seg", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac063693860.copynumber.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac063693860.copynumber.seg' - exportBins(<2 samples>, format="seg", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac034367953.copynumber.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac034367953.copynumber.seg' - exportBins(<2 samples>, format="seg", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac04b84898.copynumber.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac04b84898.copynumber.seg' - exportBins(<2 samples>, format="seg", type="segments", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac04a9c14f9.segments.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac04a9c14f9.segments.seg' - exportBins(<2 samples>, format="seg", type="segments", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac02af759a1.segments.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac02af759a1.segments.seg' - exportBins(<2 samples>, format="seg", type="segments", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac0f795133.segments.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac0f795133.segments.seg' - exportBins(<2 samples>, format="seg", type="calls", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150a.3ac01c552a6.calls.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-LGG150b.3ac01c552a6.calls.seg' - exportBins(<2 samples>, format="seg", type="calls", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-1.3ac073303e11.calls.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-2.3ac073303e11.calls.seg' - exportBins(<2 samples>, format="seg", type="calls", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-001.3ac01d3f10cb.calls.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmp6PM6Xa\QDNAseq-002.3ac01d3f10cb.calls.seg' > > message("* exportBins() ... done") * exportBins() ... done > > proc.time() user system elapsed 124.21 2.37 126.64 |
QDNAseq.Rcheck/tests_x64/QDNAseq.Rout R version 4.1.3 (2022-03-10) -- "One Push-Up" Copyright (C) 2022 The R Foundation for Statistical Computing Platform: x86_64-w64-mingw32/x64 (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(QDNAseq) > library(Biobase) ## combine(), sampleNames() 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, 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 Welcome to Bioconductor Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation("Biobase")', and for packages 'citation("pkgname")'. > library(utils) > > # Load data > data(LGG150) > data <- LGG150 > print(data) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > stopifnot(inherits(data, "QDNAseqReadCounts")) > > # Plot isobars of read counts > isobarPlot(data) Plotting sample LGG150 median read counts > > # Plot copy number profile > plot(data, ylim=c(-100, 200)) Plotting sample LGG150 (1 of 1) ... > highlightFilters(data, residual=TRUE, blacklist=TRUE) Highlighted 3,375 bins. > > # Filter out "bad" bins > dataF <- applyFilters(data, residual=TRUE, blacklist=TRUE) 38,819 total bins 38,819 of which in selected chromosomes 36,722 of which with reference sequence 33,347 final bins > print(dataF) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > plot(dataF, ylim=c(-100, 200)) Plotting sample LGG150 (1 of 1) ... > stopifnot(inherits(dataF, "QDNAseqReadCounts")) > > # Correct read counts as a function of GC content and mappability > dataC <- correctBins(dataF) Calculating correction for GC content and mappability Calculating fit for sample LGG150 (1 of 1) ... Done. > print(dataC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > plot(dataC, ylim=c(-100, 200)) Plotting sample LGG150 (1 of 1) ... > stopifnot(inherits(dataC, "QDNAseqCopyNumbers")) > > # Normalize binned read counts to have diploid normal copy number > dataN <- normalizeBins(dataC) Applying median normalization ... > print(dataN) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > plot(dataN) Plotting sample LGG150 (1 of 1) ... > stopifnot(inherits(dataN, "QDNAseqCopyNumbers")) > > # Plot noise > noisePlot(dataF) Calculating correction for GC content and mappability Calculating fit for sample LGG150 (1 of 1) ... Done. > > # Segment copy numbers > fit <- segmentBins(dataN) Performing segmentation: Segmenting: LGG150 (1 of 1) ... > print(fit) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > plot(fit) Plotting sample LGG150 (1 of 1) ... > stopifnot(inherits(fit, "QDNAseqCopyNumbers")) > > # Call copy-number segments > fitC <- callBins(fit) EM algorithm started ... [1] "Total number of segments present in the data: 10" [1] "Number of segments used for fitting the model: 9" 39066977727065208.759800308415704262427.5119.9800308413020190427.599.4 Calling iteration1: optim results time: 0 minimum: 16445.6418287481 116443.1634295677-0.939948404909672-0.5351158716347190.04999922851584940.1357341814220170.2320391157632851.492692224927890.46336036623653-0.000744748796554230.0111894143724591-0.000962583906213420.3145629342085070.798554843389167 39082027730516208.859800308415704262427.5119.9800308413020190427.599.4 Calling iteration2: optim results time: 0 minimum: 16445.5781374328 116443.1331012469-0.932876677515091-0.5359433038809970.0499979048415910.1114729434735370.1905642555481931.861013902305770.4314700360573740.0001440687684073730.01118427659401560.0007568920162792620.2061088124299370.874022351578009 39082027730516208.859800308415704262427.5119.9800308413020190427.599.4 Calling iteration3: optim results time: 0 minimum: 16445.5975371627 116443.1273697069-0.924012853099608-0.5365177469718940.04999923288882760.108573194240180.1856071014916831.753751992204390.4694950401327692.93313204138107e-050.0111878614439676-0.0001759851682342870.07360543573369820.943675664015282 EM algorithm done ... Computing posterior probabilities for all segments ... Total time:0minutes Adjusting segmented data for cellularity ... Cellularity sample1: 1 Adjusting normalized data for cellularity ... Cellularity sample1: 1 1 39108707951750208.960.7800308415704262427.5119.9800308413020190427.599.4 39108898118496208.962800308415704262427.5119.9800308413020190427.599.4 39108868118490208.962800308415704262427.5119.9800308413020190427.599.4 39109148385505208.964800308415704262427.5119.9800308413020190427.599.4 39113418386460208.964800308415704262427.5119.9800308413020190427.599.4 39113508386464208.964800308415704262427.5119.9800308413020190427.599.4 39113598386468208.964800308415704262427.5119.9800308413020190427.599.4 39113688386472208.964800308415704262427.5119.9800308413020190427.599.4 39113778386476208.964800308415704262427.5119.9800308413020190427.599.4 39113838386479208.964800308415704262427.5119.9800308413020190427.599.4 39114028453209208.964.5800308415704262427.5119.9800308413020190427.599.4 3911819845353220964.5800308415704262427.5119.9800308413020190427.599.4 FINISHED! Total time:0minutes There were 50 or more warnings (use warnings() to see the first 50) > print(fitC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: calls, copynumber, probamp, probdloss, probgain, probloss, probnorm, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > plot(fitC) Plotting sample LGG150 (1 of 1) ... > > > # --------------------------------------------------------------- > # Exporting > # --------------------------------------------------------------- > message("* exportBins() ...") * exportBins() ... > > sets <- list(data = data, dataC = dataC, fit = fit, fitC = fitC) > for (name in names(sets)) { + set <- sets[[name]] + formats <- c("tsv", "igv", "bed") + if (name == "fitC") formats <- c(formats, "vcf", "seg") + for (format in formats) { + types <- c("copynumber") + if (name %in% c("fit", "fitC")) types <- c(types, "segments") + if (name == "fitC") types <- c(types, "calls") + for (type in types) { + fileext <- sprintf(".%s.%s", type, format) + templates <- c("QDNAseq-%s.", "QDNAseq-%i.", "QDNAseq-%03i.") + if (ncol(set) == 1L || !(format %in% c("bed", "seg", "vcf"))) { + templates <- c("QDNAseq.", templates) + } + for (template in templates) { + file <- tempfile(pattern = template, fileext = fileext) + message(sprintf(" - exportBins(<%d samples>, format=\"%s\", type=\"%s\", file=\"%s\")", ncol(set), format, type, template)) + file <- exportBins(set, file = file, format = format, type = type) + message(sprintf(" File(s) written: [n=%d] %s", + length(file), paste(sQuote(file), collapse = ", "))) + stopifnot(all(file_test("-f", file))) + file.remove(file) + stopifnot(!any(file_test("-f", file))) + } + } + } + } - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4067e47cad.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d40502d62fc.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d4018db6f21.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d402a77195d.copynumber.tsv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d401175c33.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d40623e6898.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d40f0bcc0.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d403cab6a21.copynumber.igv' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d402d573c9a.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d40567843ed.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d40249b29e6.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d40345f52eb.copynumber.bed' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d404f8933c3.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4037d35ed3.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d40553f4c2d.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d404bef3b1e.copynumber.tsv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d405dd34120.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d405eac7955.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d40752f2100.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d407a56108f.copynumber.igv' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d40101f3e38.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d4013411e36.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d4067a81622.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d405db82409.copynumber.bed' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d401e9c1f27.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4040366767.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d40656b4227.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d4035d955ca.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d40103c31a.segments.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4035131292.segments.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d40533c1cf8.segments.tsv' - exportBins(<1 samples>, format="tsv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d406ea31204.segments.tsv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d40193614d7.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4078c36592.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d402865853.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d403aa31d5c.copynumber.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d409863b33.segments.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d402c1762f8.segments.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d406530284a.segments.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d403d8c316e.segments.igv' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq.") 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File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d40255a1b9.segments.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d407afa24ef.segments.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d401b927deb.segments.bed' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4057366e1a.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d404dc1038.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") 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File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d403c115259.segments.tsv' - exportBins(<1 samples>, format="tsv", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4052e62c3e.calls.tsv' - exportBins(<1 samples>, format="tsv", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4063013bd6.calls.tsv' - exportBins(<1 samples>, format="tsv", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d401c541d79.calls.tsv' - exportBins(<1 samples>, format="tsv", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d405fd91a6d.calls.tsv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4074a115f.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d404a0f4bd0.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d40591e3fd8.copynumber.igv' - exportBins(<1 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d404a678db.copynumber.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4018fb5731.segments.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d404d5e15d1.segments.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d407e157e79.segments.igv' - exportBins(<1 samples>, format="igv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d404c2837e9.segments.igv' - exportBins(<1 samples>, format="igv", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d40780f472b.calls.igv' - exportBins(<1 samples>, format="igv", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4036dc6409.calls.igv' - exportBins(<1 samples>, format="igv", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d407da420e.calls.igv' - exportBins(<1 samples>, format="igv", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d405d2e3ad1.calls.igv' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d40183b6b5a.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d4030df25db.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d404dbc621c.copynumber.bed' - exportBins(<1 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d401e306a41.copynumber.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d405ca32edb.segments.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d40489c4460.segments.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d407e531d7c.segments.bed' - exportBins(<1 samples>, format="bed", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d407fc670dc.segments.bed' - exportBins(<1 samples>, format="bed", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4023ac6e63.calls.bed' - exportBins(<1 samples>, format="bed", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d40b146e5.calls.bed' - exportBins(<1 samples>, format="bed", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d405fdf62db.calls.bed' - exportBins(<1 samples>, format="bed", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d40572f47b8.calls.bed' - exportBins(<1 samples>, format="vcf", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d40758168b8.copynumber.vcf' - exportBins(<1 samples>, format="vcf", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d40739c4768.copynumber.vcf' - exportBins(<1 samples>, format="vcf", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d4039df293b.copynumber.vcf' - exportBins(<1 samples>, format="vcf", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d4048cb12de.copynumber.vcf' - exportBins(<1 samples>, format="vcf", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4042927f35.segments.vcf' - exportBins(<1 samples>, format="vcf", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d40641371e.segments.vcf' - exportBins(<1 samples>, format="vcf", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d401153186f.segments.vcf' - exportBins(<1 samples>, format="vcf", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d4042a14dcd.segments.vcf' - exportBins(<1 samples>, format="vcf", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d403210464a.calls.vcf' - exportBins(<1 samples>, format="vcf", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d402a6872f0.calls.vcf' - exportBins(<1 samples>, format="vcf", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d407f3f41a3.calls.vcf' - exportBins(<1 samples>, format="vcf", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d406da47f7.calls.vcf' - exportBins(<1 samples>, format="seg", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d407265f9.copynumber.seg' - exportBins(<1 samples>, format="seg", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d40313d27fa.copynumber.seg' - exportBins(<1 samples>, format="seg", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d40172b27d2.copynumber.seg' - exportBins(<1 samples>, format="seg", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d4046447142.copynumber.seg' - exportBins(<1 samples>, format="seg", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d406df24a5a.segments.seg' - exportBins(<1 samples>, format="seg", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d402dce80b.segments.seg' - exportBins(<1 samples>, format="seg", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d405da6184e.segments.seg' - exportBins(<1 samples>, format="seg", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d404ad17688.segments.seg' - exportBins(<1 samples>, format="seg", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d403d112418.calls.seg' - exportBins(<1 samples>, format="seg", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150.8d4067904e28.calls.seg' - exportBins(<1 samples>, format="seg", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d404ebe533c.calls.seg' - exportBins(<1 samples>, format="seg", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d4032152e18.calls.seg' > > sets <- list(data = data, dataC = dataC, fit = fit, fitC = fitC) > sets <- lapply(sets, FUN = function(set) { + stopifnot(ncol(set) == 1L) + name <- sampleNames(set) + setA <- set + sampleNames(setA) <- sprintf("%sa", name) + setB <- set + sampleNames(setB) <- sprintf("%sb", name) + combine(setA, setB) + }) > > for (name in names(sets)) { + set <- sets[[name]] + stopifnot(ncol(set) == 2L) + formats <- c("tsv", "igv", "bed") + if (name == "fitC") formats <- c(formats, "vcf", "seg") + for (format in formats) { + types <- c("copynumber") + if (name %in% c("fit", "fitC")) types <- c(types, "segments") + if (name == "fitC") types <- c(types, "calls") + for (type in types) { + fileext <- sprintf(".%s.%s", type, format) + templates <- c("QDNAseq-%s.", "QDNAseq-%i.", "QDNAseq-%03i.") + if (ncol(set) == 1L || !(format %in% c("bed", "seg", "vcf"))) { + templates <- c("QDNAseq.", templates) + } + for (template in templates) { + file <- tempfile(pattern = template, fileext = fileext) + message(sprintf(" - exportBins(<%d samples>, format=\"%s\", type=\"%s\", file=\"%s\")", ncol(set), format, type, template)) + file <- exportBins(set, file = file, format = format, type = type) + message(sprintf(" File(s) written: [n=%d] %s", + length(file), paste(sQuote(file), collapse = ", "))) + stopifnot(all(file_test("-f", file))) + file.remove(file) + stopifnot(!any(file_test("-f", file))) + } + } + } + } - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d40410f38f2.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d405cdb1309.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d40748a414.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d4037cb5433.copynumber.tsv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d407c7443b.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d405569719a.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d40da1a26.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d4010501790.copynumber.igv' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d404f8a275b.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d404f8a275b.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d404dc7b7b.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d404dc7b7b.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d4043a01110.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d4043a01110.copynumber.bed' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d40532675d8.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4036e02a4b.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d403d357d80.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d4071a87949.copynumber.tsv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d407572682a.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4019c9c1d.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d40315d1432.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d407add1099.copynumber.igv' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d40547f5f99.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d40547f5f99.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d4028db2371.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d4028db2371.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d40479f104c.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d40479f104c.copynumber.bed' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4030e81a9e.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d40503911a9.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d404c704f01.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d407c2c2b3f.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d404a762949.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4075b314d5.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d4023287616.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d405396bae.segments.tsv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4069b7455e.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4039a24d0c.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d4010655911.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d405d5619f3.copynumber.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4032e066f8.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4042df282f.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d405ace31e3.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d4046472499.segments.igv' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d4072a93e03.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d4072a93e03.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d4044e92a95.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d4044e92a95.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d405acd2495.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d405acd2495.copynumber.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d407b2854df.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d407b2854df.segments.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d4054cf4ac0.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d4054cf4ac0.segments.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d406a604b88.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d406a604b88.segments.bed' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4039117fc1.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d405b1d733b.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d402a934645.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d404f8b21c5.copynumber.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d403d0c4d16.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d407a2e7bd4.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d40413a5afa.segments.tsv' - exportBins(<2 samples>, format="tsv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d40cd35fff.segments.tsv' - exportBins(<2 samples>, format="tsv", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d402b7631d9.calls.tsv' - exportBins(<2 samples>, format="tsv", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4073c7307.calls.tsv' - exportBins(<2 samples>, format="tsv", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d40488b2d1d.calls.tsv' - exportBins(<2 samples>, format="tsv", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d405146215d.calls.tsv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4034c81f5e.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d404d3669e4.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d404954333f.copynumber.igv' - exportBins(<2 samples>, format="igv", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d40d165f7.copynumber.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d4073c25393.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d40683162ae.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d402be55ec5.segments.igv' - exportBins(<2 samples>, format="igv", type="segments", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d402c171f5d.segments.igv' - exportBins(<2 samples>, format="igv", type="calls", file="QDNAseq.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq.8d407be62976.calls.igv' - exportBins(<2 samples>, format="igv", type="calls", file="QDNAseq-%s.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%s.8d4054d455e.calls.igv' - exportBins(<2 samples>, format="igv", type="calls", file="QDNAseq-%i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%i.8d404e931467.calls.igv' - exportBins(<2 samples>, format="igv", type="calls", file="QDNAseq-%03i.") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-%03i.8d4060442d11.calls.igv' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d4077fa399a.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d4077fa399a.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d4056883420.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d4056883420.copynumber.bed' - exportBins(<2 samples>, format="bed", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d402c3774b4.copynumber.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d402c3774b4.copynumber.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d407c3a2908.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d407c3a2908.segments.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d40588a4aa6.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d40588a4aa6.segments.bed' - exportBins(<2 samples>, format="bed", type="segments", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d4021c0fd5.segments.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d4021c0fd5.segments.bed' - exportBins(<2 samples>, format="bed", type="calls", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d4012ad748c.calls.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d4012ad748c.calls.bed' - exportBins(<2 samples>, format="bed", type="calls", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d405dbb242c.calls.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d405dbb242c.calls.bed' - exportBins(<2 samples>, format="bed", type="calls", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d40126411d5.calls.bed', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d40126411d5.calls.bed' - exportBins(<2 samples>, format="vcf", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d4073393c8f.copynumber.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d4073393c8f.copynumber.vcf' - exportBins(<2 samples>, format="vcf", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d40695545a5.copynumber.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d40695545a5.copynumber.vcf' - exportBins(<2 samples>, format="vcf", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d40682d72dd.copynumber.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d40682d72dd.copynumber.vcf' - exportBins(<2 samples>, format="vcf", type="segments", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d406d1a4377.segments.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d406d1a4377.segments.vcf' - exportBins(<2 samples>, format="vcf", type="segments", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d40601c3618.segments.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d40601c3618.segments.vcf' - exportBins(<2 samples>, format="vcf", type="segments", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d40795f07.segments.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d40795f07.segments.vcf' - exportBins(<2 samples>, format="vcf", type="calls", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d40f18296b.calls.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d40f18296b.calls.vcf' - exportBins(<2 samples>, format="vcf", type="calls", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d406183736f.calls.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d406183736f.calls.vcf' - exportBins(<2 samples>, format="vcf", type="calls", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d4058f2746c.calls.vcf', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d4058f2746c.calls.vcf' - exportBins(<2 samples>, format="seg", type="copynumber", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d401b547590.copynumber.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d401b547590.copynumber.seg' - exportBins(<2 samples>, format="seg", type="copynumber", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d4070ac689e.copynumber.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d4070ac689e.copynumber.seg' - exportBins(<2 samples>, format="seg", type="copynumber", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d4083b45b3.copynumber.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d4083b45b3.copynumber.seg' - exportBins(<2 samples>, format="seg", type="segments", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d40c2d203a.segments.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d40c2d203a.segments.seg' - exportBins(<2 samples>, format="seg", type="segments", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d401f817470.segments.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d401f817470.segments.seg' - exportBins(<2 samples>, format="seg", type="segments", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d40387a2f.segments.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d40387a2f.segments.seg' - exportBins(<2 samples>, format="seg", type="calls", file="QDNAseq-%s.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150a.8d40181e6ed0.calls.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-LGG150b.8d40181e6ed0.calls.seg' - exportBins(<2 samples>, format="seg", type="calls", file="QDNAseq-%i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-1.8d40589f1767.calls.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-2.8d40589f1767.calls.seg' - exportBins(<2 samples>, format="seg", type="calls", file="QDNAseq-%03i.") File(s) written: [n=2] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-001.8d40628a5ae.calls.seg', 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpe2YYbJ\QDNAseq-002.8d40628a5ae.calls.seg' > > message("* exportBins() ... done") * exportBins() ... done > > proc.time() user system elapsed 140.35 2.09 143.18 |
QDNAseq.Rcheck/tests_i386/QDNAseq,copyneutral.Rout R version 4.1.3 (2022-03-10) -- "One Push-Up" Copyright (C) 2022 The R Foundation for Statistical Computing Platform: i386-w64-mingw32/i386 (32-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(QDNAseq) > library(Biobase) 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, 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 Welcome to Bioconductor Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation("Biobase")', and for packages 'citation("pkgname")'. > set.seed(0xBEEF) > > data(LGG150) > data <- LGG150 > print(data) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataF <- applyFilters(data, residual=TRUE, blacklist=TRUE) 38,819 total bins 38,819 of which in selected chromosomes 36,722 of which with reference sequence 33,347 final bins > print(dataF) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataC <- correctBins(dataF) Calculating correction for GC content and mappability Calculating fit for sample LGG150 (1 of 1) ... Done. > > ## Force all copy neutral data > cn <- assayDataElement(dataC, "copynumber") > cn[,1] <- rnorm(nrow(cn), mean = 1.0, sd = 0.05) > assayDataElement(dataC, "copynumber") <- cn > > print(dataC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataN <- normalizeBins(dataC) Applying median normalization ... > print(dataN) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > fit <- segmentBins(dataN) Performing segmentation: Segmenting: LGG150 (1 of 1) ... > print(fit) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > fitC <- callBins(fit) EM algorithm started ... [1] "Total number of segments present in the data: 4" [1] "Number of segments used for fitting the model: 4" 38924065522393118.842.2808033112255594246.693.6808033110144321246.677.4 Calling iteration1: optim results time: 0 minimum: 16682.0890247004 116682.0890247004-0.825303675797091-0.323169506423803-0.001754401929814960.2970863141060160.5078724084702190.9928769615298530.1100346090918040.0003692713871108020.0111811691191362-0.0001065348234756080.1102701734224670.145866377811007 38939115524710118.942.2808033112255594246.693.6808033110144321246.677.4 Calling iteration2: optim results time: 0 minimum: 16682.0888522346 116682.0888522346-0.816384144994661-0.31848916294222-0.00167850977268490.292952991143050.5008064461942260.9819310567480430.1311557982956840.0002223141320088620.01118096583020170.0001872099918784220.1313921659017140.175722206269368 EM algorithm done ... Computing posterior probabilities for all segments ... Total time:0minutes Adjusting segmented data for cellularity ... Cellularity sample1: 1 Adjusting normalized data for cellularity ... Cellularity sample1: 1 1 3896579572800511943.8808033112255594246.693.6808033110144321246.677.4 3896598589474911945808033112255594246.693.6808033110144321246.677.4 3896595589474511945808033112255594246.693.6808033110144321246.677.4 3896623616152511947.1808033112255594246.693.6808033110144321246.677.4 3897050616216311947.1808033112255594246.693.6808033110144321246.677.4 3897059616216611947.1808033112255594246.693.6808033110144321246.677.4 3897068616216911947.1808033112255594246.693.6808033110144321246.677.4 3897077616217211947.1808033112255594246.693.6808033110144321246.677.4 3897086616217511947.1808033112255594246.693.6808033110144321246.677.4 3897092616217711947.1808033112255594246.693.6808033110144321246.677.4 3897111622889111947.6808033112255594246.693.6808033110144321246.677.4 3897528622912811947.6808033112255594246.693.6808033110144321246.677.4 FINISHED! Total time:0minutes There were 24 warnings (use warnings() to see them) > print(fitC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: calls, copynumber, probamp, probdloss, probgain, probloss, probnorm, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > > ## Assert that everything is called copy-neutral > calls <- assayDataElement(fitC, "calls") > stopifnot(all(is.na(calls) | calls == 0)) > > formats <- c("tsv", "igv", "bed", "seg", "vcf") > types <- c("copynumber", "segments", "calls") > for (format in formats) { + for (type in types) { + fileext <- sprintf(".%s.%s", type, format) + file <- tempfile(pattern = "QDNAseq-%s", fileext = fileext) + message(sprintf(" - exportBins(<%d samples>, format=\"%s\", type=\"%s\")", ncol(fitC), format, type)) + file <- exportBins(fitC, format = format, type = type, file = file) + message(sprintf(" File(s) written: [n=%d] %s", + length(file), paste(sQuote(file), collapse = ", "))) + stopifnot(all(file_test("-f", file))) + if (format == "seg") { + segs <- read.table(file, sep = "\t", header = TRUE) + print(segs) + stopifnot(nrow(segs) == 0L) + } else if (format == "vcf") { + rows <- readLines(file) + rows <- grep("^#", rows, invert = TRUE, value = TRUE) + print(rows) + stopifnot(length(rows) == 0L) + } + file.remove(file) + stopifnot(!any(file_test("-f", file))) + } + } - exportBins(<1 samples>, format="tsv", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-%sd0a8531d672b.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-%sd0a85e746e7b.segments.tsv' - exportBins(<1 samples>, format="tsv", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-%sd0a815f0693e.calls.tsv' - exportBins(<1 samples>, format="igv", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-%sd0a82280511c.copynumber.igv' - exportBins(<1 samples>, format="igv", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-%sd0a8170f1186.segments.igv' - exportBins(<1 samples>, format="igv", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-%sd0a873eb5a10.calls.igv' - exportBins(<1 samples>, format="bed", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-LGG150d0a8627f24b4.copynumber.bed' - exportBins(<1 samples>, format="bed", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-LGG150d0a853e8171f.segments.bed' - exportBins(<1 samples>, format="bed", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-LGG150d0a8412f5f7a.calls.bed' - exportBins(<1 samples>, format="seg", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-LGG150d0a821f7043.copynumber.seg' [1] SAMPLE_NAME CHROMOSOME START STOP [5] DATAPOINTS LOG2_RATIO_MEAN <0 rows> (or 0-length row.names) - exportBins(<1 samples>, format="seg", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-LGG150d0a818185c37.segments.seg' [1] SAMPLE_NAME CHROMOSOME START STOP [5] DATAPOINTS LOG2_RATIO_MEAN <0 rows> (or 0-length row.names) - exportBins(<1 samples>, format="seg", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-LGG150d0a8745a5a66.calls.seg' [1] SAMPLE_NAME CHROMOSOME START STOP [5] DATAPOINTS LOG2_RATIO_MEAN <0 rows> (or 0-length row.names) - exportBins(<1 samples>, format="vcf", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-LGG150d0a83d887bd6.copynumber.vcf' character(0) - exportBins(<1 samples>, format="vcf", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-LGG150d0a87681276c.segments.vcf' character(0) - exportBins(<1 samples>, format="vcf", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpiSkSVi\QDNAseq-LGG150d0a838bb55f3.calls.vcf' character(0) > > proc.time() user system elapsed 21.93 0.51 22.43 |
QDNAseq.Rcheck/tests_x64/QDNAseq,copyneutral.Rout R version 4.1.3 (2022-03-10) -- "One Push-Up" Copyright (C) 2022 The R Foundation for Statistical Computing Platform: x86_64-w64-mingw32/x64 (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(QDNAseq) > library(Biobase) 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, 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 Welcome to Bioconductor Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation("Biobase")', and for packages 'citation("pkgname")'. > set.seed(0xBEEF) > > data(LGG150) > data <- LGG150 > print(data) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataF <- applyFilters(data, residual=TRUE, blacklist=TRUE) 38,819 total bins 38,819 of which in selected chromosomes 36,722 of which with reference sequence 33,347 final bins > print(dataF) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataC <- correctBins(dataF) Calculating correction for GC content and mappability Calculating fit for sample LGG150 (1 of 1) ... Done. > > ## Force all copy neutral data > cn <- assayDataElement(dataC, "copynumber") > cn[,1] <- rnorm(nrow(cn), mean = 1.0, sd = 0.05) > assayDataElement(dataC, "copynumber") <- cn > > print(dataC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataN <- normalizeBins(dataC) Applying median normalization ... > print(dataN) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > fit <- segmentBins(dataN) Performing segmentation: Segmenting: LGG150 (1 of 1) ... > print(fit) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > fitC <- callBins(fit) EM algorithm started ... [1] "Total number of segments present in the data: 4" [1] "Number of segments used for fitting the model: 4" 38924067720378207.959800488414845247427.6113.3800488410184617427.677.8 Calling iteration1: optim results time: 0 minimum: 16682.0890247004 116682.0890247004-0.825303675797091-0.323169506423803-0.001754401929814960.2970863141060160.5078724084702190.9928769615298530.1100346090918040.0003692713871108020.0111811691191362-0.0001065348234756080.1102701734224670.145866377811007 3893911772379920859800488414845247427.6113.3800488410184617427.677.8 Calling iteration2: optim results time: 0 minimum: 16682.0888522346 116682.0888522346-0.816384144994661-0.31848916294222-0.00167850977268490.292952991143050.5008064461942260.9819310567480430.1311557982956840.0002223141320088620.01118096583020170.0001872099918784220.1313921659017140.175722206269368 EM algorithm done ... Computing posterior probabilities for all segments ... Total time:0minutes Adjusting segmented data for cellularity ... Cellularity sample1: 1 Adjusting normalized data for cellularity ... Cellularity sample1: 1 1 38965797945553208.160.7800488414845247427.6113.3800488410460893427.679.9 38965988112299208.261.9800488414845247427.6113.3800488410460893427.679.9 38965958112293208.261.9800488414845247427.6113.3800488410460893427.679.9 38966238379073208.264800488414845247427.6113.3800488410460893427.679.9 38970508380028208.264800488414845247427.6113.3800488410460893427.679.9 38970598380032208.264800488414845247427.6113.3800488410460893427.679.9 38970688380036208.264800488414845247427.6113.3800488410460893427.679.9 38970778380040208.264800488414845247427.6113.3800488410460893427.679.9 38970868380044208.264800488414845247427.6113.3800488410460893427.679.9 38970928380047208.264800488414845247427.6113.3800488410460893427.679.9 38971118446777208.264.5800488414845247427.6113.3800488410460893427.679.9 38975288447100208.264.5800488414845247427.6113.3800488410460893427.679.9 FINISHED! Total time:0minutes There were 24 warnings (use warnings() to see them) > print(fitC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: calls, copynumber, probamp, probdloss, probgain, probloss, probnorm, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > > ## Assert that everything is called copy-neutral > calls <- assayDataElement(fitC, "calls") > stopifnot(all(is.na(calls) | calls == 0)) > > formats <- c("tsv", "igv", "bed", "seg", "vcf") > types <- c("copynumber", "segments", "calls") > for (format in formats) { + for (type in types) { + fileext <- sprintf(".%s.%s", type, format) + file <- tempfile(pattern = "QDNAseq-%s", fileext = fileext) + message(sprintf(" - exportBins(<%d samples>, format=\"%s\", type=\"%s\")", ncol(fitC), format, type)) + file <- exportBins(fitC, format = format, type = type, file = file) + message(sprintf(" File(s) written: [n=%d] %s", + length(file), paste(sQuote(file), collapse = ", "))) + stopifnot(all(file_test("-f", file))) + if (format == "seg") { + segs <- read.table(file, sep = "\t", header = TRUE) + print(segs) + stopifnot(nrow(segs) == 0L) + } else if (format == "vcf") { + rows <- readLines(file) + rows <- grep("^#", rows, invert = TRUE, value = TRUE) + print(rows) + stopifnot(length(rows) == 0L) + } + file.remove(file) + stopifnot(!any(file_test("-f", file))) + } + } - exportBins(<1 samples>, format="tsv", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-%s62206dea59f0.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-%s622075c732b.segments.tsv' - exportBins(<1 samples>, format="tsv", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-%s622067705509.calls.tsv' - exportBins(<1 samples>, format="igv", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-%s62206aed5f68.copynumber.igv' - exportBins(<1 samples>, format="igv", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-%s622049f92b44.segments.igv' - exportBins(<1 samples>, format="igv", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-%s6220289d755c.calls.igv' - exportBins(<1 samples>, format="bed", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-LGG15062205bcd4ace.copynumber.bed' - exportBins(<1 samples>, format="bed", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-LGG150622015ee7fc6.segments.bed' - exportBins(<1 samples>, format="bed", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-LGG1506220205d7872.calls.bed' - exportBins(<1 samples>, format="seg", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-LGG1506220527c3ee0.copynumber.seg' [1] SAMPLE_NAME CHROMOSOME START STOP [5] DATAPOINTS LOG2_RATIO_MEAN <0 rows> (or 0-length row.names) - exportBins(<1 samples>, format="seg", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-LGG150622039ca746b.segments.seg' [1] SAMPLE_NAME CHROMOSOME START STOP [5] DATAPOINTS LOG2_RATIO_MEAN <0 rows> (or 0-length row.names) - exportBins(<1 samples>, format="seg", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-LGG1506220440e63da.calls.seg' [1] SAMPLE_NAME CHROMOSOME START STOP [5] DATAPOINTS LOG2_RATIO_MEAN <0 rows> (or 0-length row.names) - exportBins(<1 samples>, format="vcf", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-LGG15062203a76176.copynumber.vcf' character(0) - exportBins(<1 samples>, format="vcf", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-LGG150622027765088.segments.vcf' character(0) - exportBins(<1 samples>, format="vcf", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\Rtmpyg1wXr\QDNAseq-LGG15062204b00222b.calls.vcf' character(0) > > proc.time() user system elapsed 23.75 0.43 24.17 |
QDNAseq.Rcheck/tests_i386/QDNAseq,gain-copyneutral-gain.Rout R version 4.1.3 (2022-03-10) -- "One Push-Up" Copyright (C) 2022 The R Foundation for Statistical Computing Platform: i386-w64-mingw32/i386 (32-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(QDNAseq) > library(Biobase) 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, 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 Welcome to Bioconductor Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation("Biobase")', and for packages 'citation("pkgname")'. > library(utils) > set.seed(0xBEEF) > > data(LGG150) > data <- LGG150 > print(data) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataF <- applyFilters(data, residual=TRUE, blacklist=TRUE) 38,819 total bins 38,819 of which in selected chromosomes 36,722 of which with reference sequence 33,347 final bins > print(dataF) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataC <- correctBins(dataF) Calculating correction for GC content and mappability Calculating fit for sample LGG150 (1 of 1) ... Done. > > ## Force results to have segments gain, copy neutral, and gain. > cnAll <- assayDataElement(dataC, "copynumber") > cnAll[,1] <- rnorm(nrow(cnAll), mean = 1.0, sd = 0.05) > chr7 <- (chromosomes(dataC) == "7") > cn <- cnAll[chr7, , drop = FALSE] > n <- nrow(cn) > idxs <- seq(from=1/3*n - 0.1*n, to=1/3*n + 0.1*n) > cn[idxs,1] <- rnorm(length(idxs), mean = 2.0, sd = 0.05) > idxs <- seq(from=2/3*n - 0.1*n, to=2/3*n + 0.1*n) > cn[idxs,1] <- rnorm(length(idxs), mean = 2.0, sd = 0.05) > cnAll[chr7, ] <- cn > assayDataElement(dataC, "copynumber") <- cnAll > print(dataC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataN <- normalizeBins(dataC) Applying median normalization ... > print(dataN) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > fit <- segmentBins(dataN) Performing segmentation: Segmenting: LGG150 (1 of 1) ... > print(fit) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > fitC <- callBins(fit) EM algorithm started ... [1] "Total number of segments present in the data: 8" [1] "Number of segments used for fitting the model: 8" 38927165560450118.842.5808041112255594246.693.6808041110142942246.677.4 Calling iteration1: optim results time: 0 minimum: 16691.936015802 116691.936015802-0.76889026698241-0.310183146024425-0.01185150972096230.2885943760685340.4933553445096880.9879385470392230.0299884700901994-0.0005485736219481460.0111821966975442-4.08995447325668e-050.01000052582656670.0100005260086061 EM algorithm done ... Computing posterior probabilities for all segments ... Total time:0minutes Adjusting segmented data for cellularity ... Cellularity sample1: 1 Adjusting normalized data for cellularity ... Cellularity sample1: 1 1 3896889576588811944808041112255594246.693.6808041110142942246.677.4 3896908593263211945.3808041112255594246.693.6808041110142942246.677.4 3896905593262811945.3808041112255594246.693.6808041110142942246.677.4 3896933620115811947.4808041112255594246.693.6808041110142942246.677.4 3897360620179611947.4808041112255594246.693.6808041110142942246.677.4 3897369620179911947.4808041112255594246.693.6808041110142942246.677.4 3897378620180211947.4808041112255594246.693.6808041110142942246.677.4 3897387620180511947.4808041112255594246.693.6808041110142942246.677.4 3897396620180811947.4808041112255594246.693.6808041110142942246.677.4 3897402620181011947.4808041112255594246.693.6808041110142942246.677.4 3897421626852411947.9808041112255594246.693.6808041110142942246.677.4 3897838626876111947.9808041112255594246.693.6808041110142942246.677.4 FINISHED! Total time:0minutes There were 32 warnings (use warnings() to see them) > print(fitC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: calls, copynumber, probamp, probdloss, probgain, probloss, probnorm, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > ## Assert that everything is called copy-neutral > calls <- assayDataElement(fitC, "calls") > stopifnot(all(is.na(calls) | calls %in% c(0, 2))) > > formats <- c("tsv", "igv", "bed", "seg", "vcf") > types <- c("copynumber", "segments", "calls") > for (format in formats) { + for (type in types) { + fileext <- sprintf(".%s.%s", type, format) + file <- tempfile(pattern = "QDNAseq-%s", fileext = fileext) + message(sprintf(" - exportBins(<%d samples>, format=\"%s\", type=\"%s\")", ncol(fitC), format, type)) + file <- exportBins(fitC, format = format, type = type, file = file) + message(sprintf(" File(s) written: [n=%d] %s", + length(file), paste(sQuote(file), collapse = ", "))) + stopifnot(all(file_test("-f", file))) + + if (format == "seg") { + segs <- read.table(file, sep = "\t", header = TRUE) + print(segs) + stopifnot(all(segs$CHROMOSOME == "7"), nrow(segs) == 2L) + } else if (format == "vcf") { + segs <- read.table(file, sep = "\t", header = FALSE) + print(segs) + stopifnot(all(segs$V1 == "7"), nrow(segs) == 2L) + } + + file.remove(file) + stopifnot(!any(file_test("-f", file))) + } + } - exportBins(<1 samples>, format="tsv", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-%s687060f64866.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-%s68703910172b.segments.tsv' - exportBins(<1 samples>, format="tsv", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-%s68702cc87940.calls.tsv' - exportBins(<1 samples>, format="igv", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-%s687077cf44db.copynumber.igv' - exportBins(<1 samples>, format="igv", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-%s68706dc073d9.segments.igv' - exportBins(<1 samples>, format="igv", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-%s68702c066fe7.calls.igv' - exportBins(<1 samples>, format="bed", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-LGG15068706fe5395f.copynumber.bed' - exportBins(<1 samples>, format="bed", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-LGG150687059fb593.segments.bed' - exportBins(<1 samples>, format="bed", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-LGG150687072be18d6.calls.bed' - exportBins(<1 samples>, format="seg", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-LGG15068701fab190.copynumber.seg' SAMPLE_NAME 1 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpUX1W10\\QDNAseq-LGG15068701fab190.copynumber.seg 2 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpUX1W10\\QDNAseq-LGG15068701fab190.copynumber.seg CHROMOSOME START STOP DATAPOINTS LOG2_RATIO_MEAN 1 7 37110001 68955000 1487 0.99 2 7 90165001 122010000 2012 0.99 - exportBins(<1 samples>, format="seg", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-LGG150687077514515.segments.seg' SAMPLE_NAME 1 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpUX1W10\\QDNAseq-LGG150687077514515.segments.seg 2 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpUX1W10\\QDNAseq-LGG150687077514515.segments.seg CHROMOSOME START STOP DATAPOINTS LOG2_RATIO_MEAN 1 7 37110001 68955000 1487 0.99 2 7 90165001 122010000 2012 0.99 - exportBins(<1 samples>, format="seg", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-LGG1506870125f541f.calls.seg' SAMPLE_NAME 1 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpUX1W10\\QDNAseq-LGG1506870125f541f.calls.seg 2 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpUX1W10\\QDNAseq-LGG1506870125f541f.calls.seg CHROMOSOME START STOP DATAPOINTS LOG2_RATIO_MEAN 1 7 37110001 68955000 1487 0.99 2 7 90165001 122010000 2012 0.99 - exportBins(<1 samples>, format="vcf", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-LGG15068702a52c12.copynumber.vcf' V1 V2 V3 V4 V5 V6 V7 1 7 37110001 . <DIP> <DUP> 1000 PASS 2 7 90165001 . <DIP> <DUP> 1000 PASS V8 V9 V10 1 SVTYPE=DUP;END=68955000;SVLEN=31845000;BINS=1487;SCORE=2;LOG2CNT=0.99 GT 0/1 2 SVTYPE=DUP;END=122010000;SVLEN=31845000;BINS=2012;SCORE=2;LOG2CNT=0.99 GT 0/1 - exportBins(<1 samples>, format="vcf", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-LGG15068701a80737a.segments.vcf' V1 V2 V3 V4 V5 V6 V7 1 7 37110001 . <DIP> <DUP> 1000 PASS 2 7 90165001 . <DIP> <DUP> 1000 PASS V8 V9 V10 1 SVTYPE=DUP;END=68955000;SVLEN=31845000;BINS=1487;SCORE=2;LOG2CNT=0.99 GT 0/1 2 SVTYPE=DUP;END=122010000;SVLEN=31845000;BINS=2012;SCORE=2;LOG2CNT=0.99 GT 0/1 - exportBins(<1 samples>, format="vcf", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpUX1W10\QDNAseq-LGG15068703e941360.calls.vcf' V1 V2 V3 V4 V5 V6 V7 1 7 37110001 . <DIP> <DUP> 1000 PASS 2 7 90165001 . <DIP> <DUP> 1000 PASS V8 V9 V10 1 SVTYPE=DUP;END=68955000;SVLEN=31845000;BINS=1487;SCORE=2;LOG2CNT=0.99 GT 0/1 2 SVTYPE=DUP;END=122010000;SVLEN=31845000;BINS=2012;SCORE=2;LOG2CNT=0.99 GT 0/1 > > proc.time() user system elapsed 21.90 0.50 22.39 |
QDNAseq.Rcheck/tests_x64/QDNAseq,gain-copyneutral-gain.Rout R version 4.1.3 (2022-03-10) -- "One Push-Up" Copyright (C) 2022 The R Foundation for Statistical Computing Platform: x86_64-w64-mingw32/x64 (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(QDNAseq) > library(Biobase) 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, 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 Welcome to Bioconductor Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation("Biobase")', and for packages 'citation("pkgname")'. > library(utils) > set.seed(0xBEEF) > > data(LGG150) > data <- LGG150 > print(data) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataF <- applyFilters(data, residual=TRUE, blacklist=TRUE) 38,819 total bins 38,819 of which in selected chromosomes 36,722 of which with reference sequence 33,347 final bins > print(dataF) QDNAseqReadCounts (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: counts protocolData: none phenoData sampleNames: LGG150 varLabels: name reads used.reads expected.variance varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataC <- correctBins(dataF) Calculating correction for GC content and mappability Calculating fit for sample LGG150 (1 of 1) ... Done. > > ## Force results to have segments gain, copy neutral, and gain. > cnAll <- assayDataElement(dataC, "copynumber") > cnAll[,1] <- rnorm(nrow(cnAll), mean = 1.0, sd = 0.05) > chr7 <- (chromosomes(dataC) == "7") > cn <- cnAll[chr7, , drop = FALSE] > n <- nrow(cn) > idxs <- seq(from=1/3*n - 0.1*n, to=1/3*n + 0.1*n) > cn[idxs,1] <- rnorm(length(idxs), mean = 2.0, sd = 0.05) > idxs <- seq(from=2/3*n - 0.1*n, to=2/3*n + 0.1*n) > cn[idxs,1] <- rnorm(length(idxs), mean = 2.0, sd = 0.05) > cnAll[chr7, ] <- cn > assayDataElement(dataC, "copynumber") <- cnAll > print(dataC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > dataN <- normalizeBins(dataC) Applying median normalization ... > print(dataN) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > fit <- segmentBins(dataN) Performing segmentation: Segmenting: LGG150 (1 of 1) ... > print(fit) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: copynumber, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > fitC <- callBins(fit) EM algorithm started ... [1] "Total number of segments present in the data: 8" [1] "Number of segments used for fitting the model: 8" 38927167763957207.959.3800488414845247427.6113.3800488412294216427.693.8 Calling iteration1: optim results time: 0 minimum: 16691.936015802 116691.936015802-0.76889026698241-0.310183146024425-0.01185150972096230.2885943760685340.4933553445096880.9879385470392230.0299884700901994-0.0005485736219481460.0111821966975442-4.08995447325668e-050.01000052582656670.0100005260086061 EM algorithm done ... Computing posterior probabilities for all segments ... Total time:0minutes Adjusting segmented data for cellularity ... Cellularity sample1: 1 Adjusting normalized data for cellularity ... Cellularity sample1: 1 1 38968897988940208.261800488414845247427.6113.3800488412294216427.693.8 38969088155686208.262.3800488414845247427.6113.3800488412294216427.693.8 38969058155680208.262.3800488414845247427.6113.3800488412294216427.693.8 38969338424210208.264.3800488414845247427.6113.3800488412294216427.693.8 38973608425165208.264.3800488414845247427.6113.3800488412294216427.693.8 38973698425169208.264.3800488414845247427.6113.3800488412294216427.693.8 38973788425173208.264.3800488414845247427.6113.3800488412294216427.693.8 38973878425177208.264.3800488414845247427.6113.3800488412294216427.693.8 38973968425181208.264.3800488414845247427.6113.3800488412294216427.693.8 38974028425184208.264.3800488414845247427.6113.3800488412294216427.693.8 38974218491914208.264.8800488414845247427.6113.3800488412294216427.693.8 38978388492237208.264.8800488414845247427.6113.3800488412294216427.693.8 FINISHED! Total time:0minutes There were 32 warnings (use warnings() to see them) > print(fitC) QDNAseqCopyNumbers (storageMode: lockedEnvironment) assayData: 38819 features, 1 samples element names: calls, copynumber, probamp, probdloss, probgain, probloss, probnorm, segmented protocolData: none phenoData sampleNames: LGG150 varLabels: name reads ... loess.family (6 total) varMetadata: labelDescription featureData featureNames: 7:1-15000 7:15001-30000 ... 10:135525001-135534747 (38819 total) fvarLabels: chromosome start ... use (9 total) fvarMetadata: labelDescription experimentData: use 'experimentData(object)' Annotation: > > ## Assert that everything is called copy-neutral > calls <- assayDataElement(fitC, "calls") > stopifnot(all(is.na(calls) | calls %in% c(0, 2))) > > formats <- c("tsv", "igv", "bed", "seg", "vcf") > types <- c("copynumber", "segments", "calls") > for (format in formats) { + for (type in types) { + fileext <- sprintf(".%s.%s", type, format) + file <- tempfile(pattern = "QDNAseq-%s", fileext = fileext) + message(sprintf(" - exportBins(<%d samples>, format=\"%s\", type=\"%s\")", ncol(fitC), format, type)) + file <- exportBins(fitC, format = format, type = type, file = file) + message(sprintf(" File(s) written: [n=%d] %s", + length(file), paste(sQuote(file), collapse = ", "))) + stopifnot(all(file_test("-f", file))) + + if (format == "seg") { + segs <- read.table(file, sep = "\t", header = TRUE) + print(segs) + stopifnot(all(segs$CHROMOSOME == "7"), nrow(segs) == 2L) + } else if (format == "vcf") { + segs <- read.table(file, sep = "\t", header = FALSE) + print(segs) + stopifnot(all(segs$V1 == "7"), nrow(segs) == 2L) + } + + file.remove(file) + stopifnot(!any(file_test("-f", file))) + } + } - exportBins(<1 samples>, format="tsv", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-%s915c4822169c.copynumber.tsv' - exportBins(<1 samples>, format="tsv", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-%s915c2714b51.segments.tsv' - exportBins(<1 samples>, format="tsv", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-%s915c15c9433c.calls.tsv' - exportBins(<1 samples>, format="igv", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-%s915c31934906.copynumber.igv' - exportBins(<1 samples>, format="igv", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-%s915c4d62284e.segments.igv' - exportBins(<1 samples>, format="igv", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-%s915c715d3309.calls.igv' - exportBins(<1 samples>, format="bed", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-LGG150915c7b075eba.copynumber.bed' - exportBins(<1 samples>, format="bed", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-LGG150915c953209d.segments.bed' - exportBins(<1 samples>, format="bed", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-LGG150915c521527fc.calls.bed' - exportBins(<1 samples>, format="seg", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-LGG150915c745b503d.copynumber.seg' SAMPLE_NAME 1 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpWyH9eo\\QDNAseq-LGG150915c745b503d.copynumber.seg 2 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpWyH9eo\\QDNAseq-LGG150915c745b503d.copynumber.seg CHROMOSOME START STOP DATAPOINTS LOG2_RATIO_MEAN 1 7 37110001 68955000 1487 0.99 2 7 90165001 122010000 2012 0.99 - exportBins(<1 samples>, format="seg", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-LGG150915c36303077.segments.seg' SAMPLE_NAME 1 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpWyH9eo\\QDNAseq-LGG150915c36303077.segments.seg 2 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpWyH9eo\\QDNAseq-LGG150915c36303077.segments.seg CHROMOSOME START STOP DATAPOINTS LOG2_RATIO_MEAN 1 7 37110001 68955000 1487 0.99 2 7 90165001 122010000 2012 0.99 - exportBins(<1 samples>, format="seg", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-LGG150915c51d91c8a.calls.seg' SAMPLE_NAME 1 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpWyH9eo\\QDNAseq-LGG150915c51d91c8a.calls.seg 2 C:\\Users\\biocbuild\\bbs-3.14-bioc\\tmpdir\\RtmpWyH9eo\\QDNAseq-LGG150915c51d91c8a.calls.seg CHROMOSOME START STOP DATAPOINTS LOG2_RATIO_MEAN 1 7 37110001 68955000 1487 0.99 2 7 90165001 122010000 2012 0.99 - exportBins(<1 samples>, format="vcf", type="copynumber") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-LGG150915c55884c0b.copynumber.vcf' V1 V2 V3 V4 V5 V6 V7 1 7 37110001 . <DIP> <DUP> 1000 PASS 2 7 90165001 . <DIP> <DUP> 1000 PASS V8 V9 V10 1 SVTYPE=DUP;END=68955000;SVLEN=31845000;BINS=1487;SCORE=2;LOG2CNT=0.99 GT 0/1 2 SVTYPE=DUP;END=122010000;SVLEN=31845000;BINS=2012;SCORE=2;LOG2CNT=0.99 GT 0/1 - exportBins(<1 samples>, format="vcf", type="segments") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-LGG150915c72183d87.segments.vcf' V1 V2 V3 V4 V5 V6 V7 1 7 37110001 . <DIP> <DUP> 1000 PASS 2 7 90165001 . <DIP> <DUP> 1000 PASS V8 V9 V10 1 SVTYPE=DUP;END=68955000;SVLEN=31845000;BINS=1487;SCORE=2;LOG2CNT=0.99 GT 0/1 2 SVTYPE=DUP;END=122010000;SVLEN=31845000;BINS=2012;SCORE=2;LOG2CNT=0.99 GT 0/1 - exportBins(<1 samples>, format="vcf", type="calls") File(s) written: [n=1] 'C:\Users\biocbuild\bbs-3.14-bioc\tmpdir\RtmpWyH9eo\QDNAseq-LGG150915c385a60e9.calls.vcf' V1 V2 V3 V4 V5 V6 V7 1 7 37110001 . <DIP> <DUP> 1000 PASS 2 7 90165001 . <DIP> <DUP> 1000 PASS V8 V9 V10 1 SVTYPE=DUP;END=68955000;SVLEN=31845000;BINS=1487;SCORE=2;LOG2CNT=0.99 GT 0/1 2 SVTYPE=DUP;END=122010000;SVLEN=31845000;BINS=2012;SCORE=2;LOG2CNT=0.99 GT 0/1 > > proc.time() user system elapsed 23.79 0.53 24.31 |
QDNAseq.Rcheck/tests_i386/QDNAseq,parallel-reproducibility.Rout R version 4.1.3 (2022-03-10) -- "One Push-Up" Copyright (C) 2022 The R Foundation for Statistical Computing Platform: i386-w64-mingw32/i386 (32-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. > ###################################################################### > # This scripts asserts that for each processing step of QDNAseq > # the output/results are reproducible (numerically equal). > ###################################################################### > library("QDNAseq") > options("QDNAseq::verbose"=FALSE) > > # Load data > data(LGG150) > data <- LGG150 > > # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - > # TRUTH > # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - > # Filter out "bad" bins > dataF <- applyFilters(data, residual=TRUE, blacklist=TRUE) > > # Correct read counts as a function of GC content and mappability > dataC <- correctBins(dataF) > > # Normalize binned read counts to have diploid normal copy number > dataN <- normalizeBins(dataC) > > # Segment copy numbers > set.seed(42) ## segmentBins() relies on RNG via DNAcopy::segment() > fit <- segmentBins(dataN) > > # Call copy-number segments > fitC <- callBins(fit) There were 50 or more warnings (use warnings() to see the first 50) > > > # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - > # REPRODUCIBILITY > # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - > strategies <- c("sequential", "multisession") > if (parallelly::supportsMulticore()) strategies <- c(strategies, "multicore") > > oplan <- future::plan("list") > for (strategy in strategies) { + message(sprintf("Reproducibility with plan(\"%s\") ...", strategy)) + + future::plan(strategy) + + dataFr <- applyFilters(data, residual=TRUE, blacklist=TRUE) + stopifnot(all.equal(dataFr, dataF)) + + dataCr <- correctBins(dataF) + stopifnot(all.equal(dataCr, dataC)) + + dataNr <- normalizeBins(dataC) + stopifnot(all.equal(dataNr, dataN)) + + set.seed(42) ## segmentBins() relies on RNG via DNAcopy::segment() + fitr <- segmentBins(dataNr) + stopifnot(all.equal(fitr, fit)) + + fitCr <- callBins(fitr) + stopifnot(all.equal(fitCr, fitC)) + + message(sprintf("Reproducibility with plan(\"%s\") ... done", strategy)) + } Reproducibility with plan("sequential") ... Reproducibility with plan("sequential") ... done Reproducibility with plan("multisession") ... Calculating fit for sample LGG150 (1 of 1) ... Segmenting: LGG150 (1 of 1) ... Reproducibility with plan("multisession") ... done There were 50 or more warnings (use warnings() to see the first 50) > > future::plan(oplan) > > proc.time() user system elapsed 55.64 0.64 71.07 |
QDNAseq.Rcheck/tests_x64/QDNAseq,parallel-reproducibility.Rout R version 4.1.3 (2022-03-10) -- "One Push-Up" Copyright (C) 2022 The R Foundation for Statistical Computing Platform: x86_64-w64-mingw32/x64 (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. > ###################################################################### > # This scripts asserts that for each processing step of QDNAseq > # the output/results are reproducible (numerically equal). > ###################################################################### > library("QDNAseq") > options("QDNAseq::verbose"=FALSE) > > # Load data > data(LGG150) > data <- LGG150 > > # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - > # TRUTH > # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - > # Filter out "bad" bins > dataF <- applyFilters(data, residual=TRUE, blacklist=TRUE) > > # Correct read counts as a function of GC content and mappability > dataC <- correctBins(dataF) > > # Normalize binned read counts to have diploid normal copy number > dataN <- normalizeBins(dataC) > > # Segment copy numbers > set.seed(42) ## segmentBins() relies on RNG via DNAcopy::segment() > fit <- segmentBins(dataN) > > # Call copy-number segments > fitC <- callBins(fit) There were 50 or more warnings (use warnings() to see the first 50) > > > # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - > # REPRODUCIBILITY > # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - > strategies <- c("sequential", "multisession") > if (parallelly::supportsMulticore()) strategies <- c(strategies, "multicore") > > oplan <- future::plan("list") > for (strategy in strategies) { + message(sprintf("Reproducibility with plan(\"%s\") ...", strategy)) + + future::plan(strategy) + + dataFr <- applyFilters(data, residual=TRUE, blacklist=TRUE) + stopifnot(all.equal(dataFr, dataF)) + + dataCr <- correctBins(dataF) + stopifnot(all.equal(dataCr, dataC)) + + dataNr <- normalizeBins(dataC) + stopifnot(all.equal(dataNr, dataN)) + + set.seed(42) ## segmentBins() relies on RNG via DNAcopy::segment() + fitr <- segmentBins(dataNr) + stopifnot(all.equal(fitr, fit)) + + fitCr <- callBins(fitr) + stopifnot(all.equal(fitCr, fitC)) + + message(sprintf("Reproducibility with plan(\"%s\") ... done", strategy)) + } Reproducibility with plan("sequential") ... Reproducibility with plan("sequential") ... done Reproducibility with plan("multisession") ... Calculating fit for sample LGG150 (1 of 1) ... Segmenting: LGG150 (1 of 1) ... Reproducibility with plan("multisession") ... done There were 50 or more warnings (use warnings() to see the first 50) > > future::plan(oplan) > > proc.time() user system elapsed 53.60 0.56 64.54 |
QDNAseq.Rcheck/examples_i386/QDNAseq-Ex.timings
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QDNAseq.Rcheck/examples_x64/QDNAseq-Ex.timings
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