Daoud Sie
| Snapshot Date: 2019-04-08 17:01:18 -0400 (Mon, 08 Apr 2019) |
| URL: https://git.bioconductor.org/packages/QDNAseq |
| Branch: master |
| Last Commit: 0cc3216 |
| Last Changed Date: 2018-10-30 11:54:32 -0400 (Tue, 30 Oct 2018) |
| Back to Multiple platform build/check report for BioC 3.9 |
|
This page was generated on 2019-04-09 11:38:01 -0400 (Tue, 09 Apr 2019).
| Package 1258/1703 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||
| QDNAseq 1.19.0 Daoud Sie
| malbec2 | Linux (Ubuntu 18.04.2 LTS) / x86_64 | OK | OK | [ WARNINGS ] | | ||||||
| tokay2 | Windows Server 2012 R2 Standard / x64 | OK | OK | WARNINGS | OK | | ||||||
| celaya2 | OS X 10.11.6 El Capitan / x86_64 | OK | OK | WARNINGS | OK | | ||||||
| merida2 | OS X 10.11.6 El Capitan / x86_64 | OK | OK | WARNINGS | OK |
| Package: QDNAseq |
| Version: 1.19.0 |
| Command: /home/biocbuild/bbs-3.9-bioc/R/bin/R CMD check --install=check:QDNAseq.install-out.txt --library=/home/biocbuild/bbs-3.9-bioc/R/library --no-vignettes --timings QDNAseq_1.19.0.tar.gz |
| StartedAt: 2019-04-09 02:54:29 -0400 (Tue, 09 Apr 2019) |
| EndedAt: 2019-04-09 02:57:51 -0400 (Tue, 09 Apr 2019) |
| EllapsedTime: 201.2 seconds |
| RetCode: 0 |
| Status: WARNINGS |
| CheckDir: QDNAseq.Rcheck |
| Warnings: 1 |
##############################################################################
##############################################################################
###
### Running command:
###
### /home/biocbuild/bbs-3.9-bioc/R/bin/R CMD check --install=check:QDNAseq.install-out.txt --library=/home/biocbuild/bbs-3.9-bioc/R/library --no-vignettes --timings QDNAseq_1.19.0.tar.gz
###
##############################################################################
##############################################################################
* using log directory ‘/home/biocbuild/bbs-3.9-bioc/meat/QDNAseq.Rcheck’
* using R Under development (unstable) (2019-03-18 r76245)
* using platform: x86_64-pc-linux-gnu (64-bit)
* using session charset: UTF-8
* using option ‘--no-vignettes’
* checking for file ‘QDNAseq/DESCRIPTION’ ... OK
* this is package ‘QDNAseq’ version ‘1.19.0’
* 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 for sufficient/correct file permissions ... 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
* 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 files in ‘vignettes’ ... OK
* checking examples ... OK
Examples with CPU or elapsed time > 5s
user system elapsed
callBins 16.207 0.040 16.248
frequencyPlot 14.037 0.016 14.065
segmentBins 5.965 0.004 5.971
normalizeSegmentedBins 5.761 0.000 5.770
* checking for unstated dependencies in ‘tests’ ... OK
* checking tests ...
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: 1 WARNING
See
‘/home/biocbuild/bbs-3.9-bioc/meat/QDNAseq.Rcheck/00check.log’
for details.
QDNAseq.Rcheck/00install.out
############################################################################## ############################################################################## ### ### Running command: ### ### /home/biocbuild/bbs-3.9-bioc/R/bin/R CMD INSTALL QDNAseq ### ############################################################################## ############################################################################## * installing to library ‘/home/biocbuild/bbs-3.9-bioc/R/library’ * installing *source* package ‘QDNAseq’ ... ** using staged installation ** R ** data ** inst ** byte-compile and prepare package for lazy loading ** help *** installing help indices ** building package indices ** installing vignettes ** testing if installed package can be loaded from temporary location ** testing if installed package can be loaded from final location ** testing if installed package keeps a record of temporary installation path * DONE (QDNAseq)
QDNAseq.Rcheck/tests/QDNAseq,reproducibility.Rout
R Under development (unstable) (2019-03-18 r76245) -- "Unsuffered Consequences"
Copyright (C) 2019 The R Foundation for Statistical Computing
Platform: x86_64-pc-linux-gnu (64-bit)
R is free software and comes with ABSOLUTELY NO WARRANTY.
You are welcome to redistribute it under certain conditions.
Type 'license()' or 'licence()' for distribution details.
R is a collaborative project with many contributors.
Type 'contributors()' for more information and
'citation()' on how to cite R or R packages in publications.
Type 'demo()' for some demos, 'help()' for on-line help, or
'help.start()' for an HTML browser interface to help.
Type 'q()' to quit R.
> ######################################################################
> # 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
8.589 0.156 8.734
QDNAseq.Rcheck/tests/QDNAseq.Rout
R Under development (unstable) (2019-03-18 r76245) -- "Unsuffered Consequences"
Copyright (C) 2019 The R Foundation for Statistical Computing
Platform: x86_64-pc-linux-gnu (64-bit)
R is free software and comes with ABSOLUTELY NO WARRANTY.
You are welcome to redistribute it under certain conditions.
Type 'license()' or 'licence()' for distribution details.
R is a collaborative project with many contributors.
Type 'contributors()' for more information and
'citation()' on how to cite R or R packages in publications.
Type 'demo()' for some demos, 'help()' for on-line help, or
'help.start()' for an HTML browser interface to help.
Type 'q()' to quit R.
> library("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
10.442 0.164 10.597
QDNAseq.Rcheck/QDNAseq-Ex.timings
| name | user | system | elapsed | |
| addPhenodata | 0.215 | 0.000 | 0.215 | |
| applyFilters | 0.297 | 0.004 | 0.302 | |
| binReadCounts | 0 | 0 | 0 | |
| callBins | 16.207 | 0.040 | 16.248 | |
| compareToReference | 0.965 | 0.008 | 0.972 | |
| correctBins | 0.690 | 0.004 | 0.695 | |
| createBins | 0 | 0 | 0 | |
| estimateCorrection | 0.617 | 0.004 | 0.622 | |
| exportBins | 0 | 0 | 0 | |
| frequencyPlot | 14.037 | 0.016 | 14.065 | |
| getBinAnnotations | 0 | 0 | 0 | |
| highlightFilters | 0.634 | 0.012 | 0.646 | |
| isobarPlot | 0.459 | 0.000 | 0.460 | |
| makeCgh | 0.743 | 0.016 | 0.758 | |
| noisePlot | 0.622 | 0.012 | 0.633 | |
| normalizeBins | 0.810 | 0.008 | 0.818 | |
| normalizeSegmentedBins | 5.761 | 0.000 | 5.770 | |
| plot | 1.580 | 0.000 | 1.581 | |
| poolRuns | 0.223 | 0.000 | 0.223 | |
| segmentBins | 5.965 | 0.004 | 5.971 | |
| smoothOutlierBins | 1.106 | 0.011 | 1.120 | |