Daoud Sie
| Snapshot Date: 2018-04-11 16:45:18 -0400 (Wed, 11 Apr 2018) |
| URL: https://git.bioconductor.org/packages/QDNAseq |
| Branch: RELEASE_3_6 |
| Last Commit: fb0f343 |
| Last Changed Date: 2017-10-30 12:40:12 -0400 (Mon, 30 Oct 2017) |
| Back to Multiple platform build/check report for BioC 3.6 |
|
This page was generated on 2018-04-12 13:23:58 -0400 (Thu, 12 Apr 2018).
| Package 1095/1472 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||
| QDNAseq 1.14.0 Daoud Sie
| malbec1 | Linux (Ubuntu 16.04.1 LTS) / x86_64 | OK | OK | WARNINGS | | ||||||
| tokay1 | Windows Server 2012 R2 Standard / x64 | OK | OK | [ WARNINGS ] | OK | | ||||||
| veracruz1 | OS X 10.11.6 El Capitan / x86_64 | OK | OK | WARNINGS | OK | |
| Package: QDNAseq |
| Version: 1.14.0 |
| Command: rm -rf QDNAseq.buildbin-libdir QDNAseq.Rcheck && mkdir QDNAseq.buildbin-libdir QDNAseq.Rcheck && C:\Users\biocbuild\bbs-3.6-bioc\R\bin\R.exe CMD INSTALL --build --merge-multiarch --library=QDNAseq.buildbin-libdir QDNAseq_1.14.0.tar.gz >QDNAseq.Rcheck\00install.out 2>&1 && cp QDNAseq.Rcheck\00install.out QDNAseq-install.out && C:\Users\biocbuild\bbs-3.6-bioc\R\bin\R.exe CMD check --library=QDNAseq.buildbin-libdir --install="check:QDNAseq-install.out" --force-multiarch --no-vignettes --timings QDNAseq_1.14.0.tar.gz |
| StartedAt: 2018-04-12 02:22:27 -0400 (Thu, 12 Apr 2018) |
| EndedAt: 2018-04-12 02:27:25 -0400 (Thu, 12 Apr 2018) |
| EllapsedTime: 298.3 seconds |
| RetCode: 0 |
| Status: WARNINGS |
| CheckDir: QDNAseq.Rcheck |
| Warnings: 2 |
##############################################################################
##############################################################################
###
### Running command:
###
### rm -rf QDNAseq.buildbin-libdir QDNAseq.Rcheck && mkdir QDNAseq.buildbin-libdir QDNAseq.Rcheck && C:\Users\biocbuild\bbs-3.6-bioc\R\bin\R.exe CMD INSTALL --build --merge-multiarch --library=QDNAseq.buildbin-libdir QDNAseq_1.14.0.tar.gz >QDNAseq.Rcheck\00install.out 2>&1 && cp QDNAseq.Rcheck\00install.out QDNAseq-install.out && C:\Users\biocbuild\bbs-3.6-bioc\R\bin\R.exe CMD check --library=QDNAseq.buildbin-libdir --install="check:QDNAseq-install.out" --force-multiarch --no-vignettes --timings QDNAseq_1.14.0.tar.gz
###
##############################################################################
##############################################################################
* using log directory 'C:/Users/biocbuild/bbs-3.6-bioc/meat/QDNAseq.Rcheck'
* using R version 3.4.4 (2018-03-15)
* 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 '1.14.0'
* 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 ... WARNING
Found the following significant warnings:
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/applyFilters.Rd:31: missing file link 'madDiff'
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/binReadCounts.Rd:28: missing file link 'AnnotatedDataFrame'
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/estimateCorrection.Rd:43: missing file link 'madDiff'
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/getBinAnnotations.Rd:43: missing file link 'AnnotatedDataFrame'
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/highlightFilters.Rd:32: missing file link 'madDiff'
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/makeCgh.Rd:37: missing file link 'cghRaw'
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/makeCgh.Rd:38: missing file link 'cghSeg'
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/makeCgh.Rd:39: missing file link 'cghCall'
See 'C:/Users/biocbuild/bbs-3.6-bioc/meat/QDNAseq.Rcheck/00install.out' for details.
* checking installed package size ... OK
* checking package directory ... OK
* checking 'build' directory ... OK
* checking DESCRIPTION meta-information ... OK
* checking top-level files ... OK
* checking for left-over files ... OK
* checking index information ... OK
* checking package subdirectories ... 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 ... WARNING
Undocumented code objects:
'exportVCF'
All user-level objects in a package should have documentation entries.
See chapter 'Writing R documentation files' in the 'Writing R
Extensions' manual.
* checking for code/documentation mismatches ... 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 installed files from 'inst/doc' ... OK
* checking files in 'vignettes' ... OK
* checking examples ...
** running examples for arch 'i386' ... OK
Examples with CPU or elapsed time > 5s
user system elapsed
frequencyPlot 14.27 0.01 14.30
callBins 14.17 0.06 14.23
normalizeSegmentedBins 7.41 0.03 7.44
segmentBins 7.07 0.02 7.08
** running examples for arch 'x64' ... OK
Examples with CPU or elapsed time > 5s
user system elapsed
frequencyPlot 15.42 0.11 15.53
callBins 15.31 0.06 15.38
normalizeSegmentedBins 5.53 0.03 5.56
* checking for unstated dependencies in 'tests' ... OK
* checking tests ...
** running tests for arch 'i386' ...
Running 'QDNAseq,reproducibility.R'
Running 'QDNAseq.R'
OK
** running tests for arch 'x64' ...
Running 'QDNAseq,reproducibility.R'
Running 'QDNAseq.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: 2 WARNINGs
See
'C:/Users/biocbuild/bbs-3.6-bioc/meat/QDNAseq.Rcheck/00check.log'
for details.
QDNAseq.Rcheck/00install.out
install for i386
* installing *source* package 'QDNAseq' ...
** R
** data
** inst
** preparing 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
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/applyFilters.Rd:31: missing file link 'madDiff'
binReadCounts html
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/binReadCounts.Rd:28: missing file link 'AnnotatedDataFrame'
callBins html
compareToReference html
correctBins html
createBins html
estimateCorrection html
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/estimateCorrection.Rd:43: missing file link 'madDiff'
exportBins html
finding level-2 HTML links ... done
frequencyPlot html
getBinAnnotations html
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/getBinAnnotations.Rd:43: missing file link 'AnnotatedDataFrame'
highlightFilters html
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/highlightFilters.Rd:32: missing file link 'madDiff'
isobarPlot html
makeCgh html
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/makeCgh.Rd:37: missing file link 'cghRaw'
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/makeCgh.Rd:38: missing file link 'cghSeg'
Rd warning: C:/Users/biocbuild/bbs-3.6-bioc/tmpdir/RtmpqY6zev/R.INSTALL36ac55187cd7/QDNAseq/man/makeCgh.Rd:39: missing file link 'cghCall'
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
In R CMD INSTALL
install for x64
* installing *source* package 'QDNAseq' ...
** testing if installed package can be loaded
* MD5 sums
packaged installation of 'QDNAseq' as QDNAseq_1.14.0.zip
* DONE (QDNAseq)
In R CMD INSTALL
In R CMD INSTALL
|
QDNAseq.Rcheck/tests_i386/QDNAseq.Rout
R version 3.4.4 (2018-03-15) -- "Someone to Lean On"
Copyright (C) 2018 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")
>
> # 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)
> #print(fitC)
> #plot(fitC)
>
> proc.time()
user system elapsed
12.35 0.28 12.62
|
QDNAseq.Rcheck/tests_x64/QDNAseq.Rout
R version 3.4.4 (2018-03-15) -- "Someone to Lean On"
Copyright (C) 2018 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")
>
> # 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)
> #print(fitC)
> #plot(fitC)
>
> proc.time()
user system elapsed
13.06 0.18 13.23
|
|
QDNAseq.Rcheck/tests_i386/QDNAseq,reproducibility.Rout
R version 3.4.4 (2018-03-15) -- "Someone to Lean On"
Copyright (C) 2018 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")
>
> # Load data
> data(LGG150)
> data <- LGG150
>
> # 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
> dataFr <- 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
> stopifnot(all.equal(dataFr, dataF))
>
> # 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.
> dataCr <- correctBins(dataF)
Calculating correction for GC content and mappability
Calculating fit for sample LGG150 (1 of 1) ...
Done.
> stopifnot(all.equal(dataCr, dataC))
>
> # Normalize binned read counts to have diploid normal copy number
> dataN <- normalizeBins(dataC)
Applying median normalization ...
> dataNr <- normalizeBins(dataC)
Applying median normalization ...
> stopifnot(all.equal(dataNr, dataN))
>
> proc.time()
user system elapsed
6.59 0.15 6.75
|
QDNAseq.Rcheck/tests_x64/QDNAseq,reproducibility.Rout
R version 3.4.4 (2018-03-15) -- "Someone to Lean On"
Copyright (C) 2018 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")
>
> # Load data
> data(LGG150)
> data <- LGG150
>
> # 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
> dataFr <- 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
> stopifnot(all.equal(dataFr, dataF))
>
> # 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.
> dataCr <- correctBins(dataF)
Calculating correction for GC content and mappability
Calculating fit for sample LGG150 (1 of 1) ...
Done.
> stopifnot(all.equal(dataCr, dataC))
>
> # Normalize binned read counts to have diploid normal copy number
> dataN <- normalizeBins(dataC)
Applying median normalization ...
> dataNr <- normalizeBins(dataC)
Applying median normalization ...
> stopifnot(all.equal(dataNr, dataN))
>
> proc.time()
user system elapsed
6.82 0.20 7.01
|
|
QDNAseq.Rcheck/examples_i386/QDNAseq-Ex.timings
|
QDNAseq.Rcheck/examples_x64/QDNAseq-Ex.timings
|