Back to Multiple platform build/check report for BioC 3.14
ABCDEFGHIJKLMNOPQRS[T]UVWXYZ

This page was generated on 2022-01-19 13:07:31 -0500 (Wed, 19 Jan 2022).

HostnameOSArch (*)R versionInstalled pkgs
nebbiolo2Linux (Ubuntu 20.04.4 LTS)x86_644.1.2 (2021-11-01) -- "Bird Hippie" 4328
tokay2Windows Server 2012 R2 Standardx644.1.2 (2021-11-01) -- "Bird Hippie" 4077
machv2macOS 10.14.6 Mojavex86_644.1.2 (2021-11-01) -- "Bird Hippie" 4138
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

CHECK results for TitanCNA on tokay2


To the developers/maintainers of the TitanCNA package:
- Please allow up to 24 hours (and sometimes 48 hours) for your latest push to git@git.bioconductor.org:packages/TitanCNA.git to
reflect on this report. See How and When does the builder pull? When will my changes propagate? here for more information.
- Make sure to use the following settings in order to reproduce any error or warning you see on this page.

raw results

Package 1963/2083HostnameOS / ArchINSTALLBUILDCHECKBUILD BIN
TitanCNA 1.32.0  (landing page)
Gavin Ha
Snapshot Date: 2022-01-18 01:55:07 -0500 (Tue, 18 Jan 2022)
git_url: https://git.bioconductor.org/packages/TitanCNA
git_branch: RELEASE_3_14
git_last_commit: 5fd6845
git_last_commit_date: 2021-10-26 12:13:15 -0500 (Tue, 26 Oct 2021)
nebbiolo2Linux (Ubuntu 20.04.4 LTS) / x86_64  OK    OK    WARNINGS  UNNEEDED, same version is already published
tokay2Windows Server 2012 R2 Standard / x64  OK    OK    WARNINGS    OK  UNNEEDED, same version is already published
machv2macOS 10.14.6 Mojave / x86_64  OK    OK    WARNINGS    OK  UNNEEDED, same version is already published

Summary

Package: TitanCNA
Version: 1.32.0
Command: C:\Users\biocbuild\bbs-3.14-bioc\R\bin\R.exe CMD check --force-multiarch --install=check:TitanCNA.install-out.txt --library=C:\Users\biocbuild\bbs-3.14-bioc\R\library --no-vignettes --timings TitanCNA_1.32.0.tar.gz
StartedAt: 2022-01-19 03:48:01 -0500 (Wed, 19 Jan 2022)
EndedAt: 2022-01-19 03:56:53 -0500 (Wed, 19 Jan 2022)
EllapsedTime: 532.0 seconds
RetCode: 0
Status:   WARNINGS  
CheckDir: TitanCNA.Rcheck
Warnings: 2

Command output

##############################################################################
##############################################################################
###
### Running command:
###
###   C:\Users\biocbuild\bbs-3.14-bioc\R\bin\R.exe CMD check --force-multiarch --install=check:TitanCNA.install-out.txt --library=C:\Users\biocbuild\bbs-3.14-bioc\R\library --no-vignettes --timings TitanCNA_1.32.0.tar.gz
###
##############################################################################
##############################################################################


* using log directory 'C:/Users/biocbuild/bbs-3.14-bioc/meat/TitanCNA.Rcheck'
* using R version 4.1.2 (2021-11-01)
* using platform: x86_64-w64-mingw32 (64-bit)
* using session charset: ISO8859-1
* using option '--no-vignettes'
* checking for file 'TitanCNA/DESCRIPTION' ... OK
* checking extension type ... Package
* this is package 'TitanCNA' version '1.32.0'
* 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 'TitanCNA' can be installed ... WARNING
Found the following significant warnings:
  Warning: replacing previous import 'GenomicRanges::shift' by 'data.table::shift' when loading 'TitanCNA'
  Warning: replacing previous import 'IRanges::collapse' by 'dplyr::collapse' when loading 'TitanCNA'
  Warning: replacing previous import 'data.table::last' by 'dplyr::last' when loading 'TitanCNA'
  Warning: replacing previous import 'GenomicRanges::union' by 'dplyr::union' when loading 'TitanCNA'
  Warning: replacing previous import 'IRanges::slice' by 'dplyr::slice' when loading 'TitanCNA'
  Warning: replacing previous import 'GenomeInfoDb::intersect' by 'dplyr::intersect' when loading 'TitanCNA'
  Warning: replacing previous import 'GenomicRanges::setdiff' by 'dplyr::setdiff' when loading 'TitanCNA'
  Warning: replacing previous import 'data.table::first' by 'dplyr::first' when loading 'TitanCNA'
  Warning: replacing previous import 'IRanges::desc' by 'dplyr::desc' when loading 'TitanCNA'
  Warning: replacing previous import 'BiocGenerics::combine' by 'dplyr::combine' when loading 'TitanCNA'
  Warning: replacing previous import 'data.table::between' by 'dplyr::between' when loading 'TitanCNA'
  Warning: replacing previous import 'dplyr::select' by 'VariantAnnotation::select' when loading 'TitanCNA'
See 'C:/Users/biocbuild/bbs-3.14-bioc/meat/TitanCNA.Rcheck/00install.out' for details.
* checking installed package size ... NOTE
  installed size is  7.3Mb
  sub-directories of 1Mb or more:
    data      1.7Mb
    extdata   4.9Mb
* 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 ... NOTE
computeSDbwIndex: no visible binding for global variable
  'ClonalCluster'
correctIntegerCN: no visible binding for global variable
  'Median_HaplotypeRatio'
correctIntegerCN: no visible binding for global variable 'Chromosome'
correctIntegerCN: no visible binding for global variable 'Copy_Number'
correctIntegerCN: no visible binding for global variable
  'logR_Copy_Number'
correctIntegerCN: no visible binding for global variable 'Median_logR'
correctIntegerCN: no visible binding for global variable
  'Cellular_Prevalence'
correctIntegerCN: no visible binding for global variable 'Chr'
correctIntegerCN: no visible binding for global variable 'LogRatio'
correctIntegerCN: no visible binding for global variable
  'CellularPrevalence'
correctIntegerCN: no visible binding for global variable
  'Corrected_Ratio'
correctIntegerCN: no visible binding for global variable
  'Corrected_Copy_Number'
correctIntegerCN: no visible binding for global variable
  'Corrected_Call'
correctIntegerCN: no visible binding for global variable 'TITAN_call'
correctIntegerCN: no visible binding for global variable
  'Corrected_MajorCN'
correctIntegerCN: no visible binding for global variable 'MajorCN'
correctIntegerCN: no visible binding for global variable
  'Corrected_MinorCN'
correctIntegerCN: no visible binding for global variable 'MinorCN'
correctIntegerCN: no visible binding for global variable 'CopyNumber'
correctIntegerCN: no visible binding for global variable 'TITANcall'
correctReadDepth: no visible global function definition for 'queryHits'
correctReadcount: no visible global function definition for 'loess'
correctReadcount: no visible global function definition for 'predict'
correctReadcount: no visible global function definition for 'approxfun'
correctReadcount: no visible global function definition for 'lowess'
extendSegments: no visible binding for global variable 'Start'
extendSegments: no visible binding for global variable 'End'
extendSegments: no visible binding for global variable 'Chromosome'
extendSegments: no visible binding for global variable 'Start.snp'
extendSegments: no visible binding for global variable 'End.snp'
extendSegments: no visible binding for global variable 'Start.telo'
extendSegments: no visible binding for global variable 'seq.info'
extractAlleleReadCounts: no visible global function definition for
  'PileupParam'
extractAlleleReadCounts: no visible global function definition for
  'BcfFile'
extractAlleleReadCounts: no visible global function definition for
  'scanBcf'
extractAlleleReadCounts: no visible global function definition for
  'ScanBamParam'
extractAlleleReadCounts: no visible global function definition for
  'scanBamFlag'
extractAlleleReadCounts: no visible global function definition for
  'BamFile'
extractAlleleReadCounts: no visible global function definition for
  'pileup'
extractAlleleReadCounts: no visible global function definition for
  'write.table'
getHaplotypesFromVCF: no visible global function definition for
  'rowRanges<-'
getHaplotypesFromVCF: no visible global function definition for
  'rowRanges'
getHaplotypesFromVCF: no visible global function definition for
  'na.omit'
getHaplotypesFromVCF: no visible global function definition for
  'unstrsplit'
getHaplotypesFromVCF: no visible global function definition for
  'queryHits'
getHaplotypesFromVCF: no visible global function definition for
  'DataFrame'
getOverlap: no visible global function definition for 'as'
getOverlap: no visible global function definition for 'queryHits'
getOverlap: no visible global function definition for 'subjectHits'
getPositionOverlap: no visible global function definition for 'as'
getSubcloneProfiles: no visible global function definition for
  'read.delim'
getSubcloneProfiles: no visible binding for global variable
  'CopyNumber'
getSubcloneProfiles: no visible binding for global variable 'TITANcall'
keepChr: no visible global function definition for 'as'
loadAlleleCounts: no visible global function definition for
  'read.delim'
loadBXcountsFromBEDDir: no visible binding for global variable
  'BXcounts'
loadBXcountsFromBEDDir: no visible binding for global variable 'BX'
loadBXcountsFromBEDDir: no visible global function definition for
  'RangedData'
loadHaplotypeAlleleCounts: no visible global function definition for
  'read.delim'
loadHaplotypeAlleleCounts: no visible global function definition for
  'subjectHits'
loadHaplotypeAlleleCounts: no visible global function definition for
  'as'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'phasedAlleleFraction'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'phasedCount'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'depth'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'SNPs'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'HaplotypeFraction'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'HaplotypeDepth.sum'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'HaplotypeBinDepth.sum'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'HaplotypeDepth.mean'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'HaplotypeBinDepth.mean'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'phaseSet'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'haplotypeBin'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'HaplotypeFraction.symmetric'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'HaplotypeDepth.sum.symmetric'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'HaplotypeDepth.mean.symmetric'
loadHaplotypeAlleleCounts: no visible global function definition for
  '.'
loadHaplotypeAlleleCounts: no visible global function definition for
  'na.omit'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'phasedCount.haploSymmetric'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'nonRef'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'phaseSet.aggr'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'HaplotypeRatio'
loadHaplotypeAlleleCounts: no visible binding for global variable
  'tumDepth'
loadReadCountsFromBed: no visible global function definition for
  'excludeCentromere'
loadReadCountsFromBed: no visible global function definition for
  'filterByTargetedSequences'
mergeSegsByCol: no visible binding for global variable 'Median_Ratio'
mergeSegsByCol: no visible binding for global variable 'Median_logR'
mergeSegsByCol: no visible binding for global variable 'End'
mergeSegsByCol: no visible binding for global variable 'Length.snp.'
outlierObslik: no visible global function definition for 'dunif'
outputModelParameters: no visible global function definition for
  'write.table'
outputTitanResults: no visible global function definition for
  'write.table'
outputTitanSegments: no visible binding for global variable 'Sample'
plotAllelicCN: no visible binding for global variable 'Allele.1'
plotAllelicCN: no visible binding for global variable 'LogRatio'
plotAllelicCN: no visible binding for global variable 'Allele.2'
plotAllelicCN: no visible binding for global variable 'Chr'
plotAllelicCN: no visible binding for global variable 'TITANcall'
plotAllelicCN: no visible global function definition for 'par'
plotAllelicCN: no visible binding for global variable 'CopyNumber'
plotAllelicCN: no visible global function definition for 'points'
plotAllelicCN: no visible global function definition for 'lines'
plotAllelicRatio: no visible binding for global variable 'Chr'
plotAllelicRatio: no visible binding for global variable 'TITANcall'
plotAllelicRatio: no visible global function definition for 'par'
plotAllelicRatio: no visible binding for global variable 'AllelicRatio'
plotAllelicRatio: no visible global function definition for 'lines'
plotCNlogRByChr: no visible binding for global variable 'LogRatio'
plotCNlogRByChr: no visible binding for global variable 'Median_logR'
plotCNlogRByChr: no visible binding for global variable 'Chr'
plotCNlogRByChr: no visible binding for global variable 'TITANcall'
plotCNlogRByChr: no visible global function definition for 'par'
plotCNlogRByChr: no visible global function definition for 'lines'
plotCNlogRByChr: no visible binding for global variable 'Chromosome'
plotCNlogRByChr : <anonymous>: no visible global function definition
  for 'lines'
plotCNlogRByChr: no visible binding for global variable
  'End_Position.bp.'
plotCNlogRByChr: no visible binding for global variable
  'Start_Position.bp.'
plotChrLines: no visible global function definition for 'lines'
plotChrLines: no visible global function definition for 'axis'
plotClonalFrequency: no visible binding for global variable
  'ClonalCluster'
plotClonalFrequency: no visible binding for global variable
  'CellularPrevalence'
plotClonalFrequency: no visible binding for global variable 'TITANcall'
plotClonalFrequency: no visible binding for global variable 'Chr'
plotClonalFrequency: no visible global function definition for 'par'
plotClonalFrequency: no visible global function definition for 'lines'
plotClonalFrequency: no visible global function definition for 'mtext'
plotGeneAnnotation: no visible global function definition for 'abline'
plotGeneAnnotation: no visible global function definition for 'mtext'
plotHaplotypeFraction: no visible binding for global variable
  'HaplotypeRatio.1'
plotHaplotypeFraction: no visible binding for global variable
  'HaplotypeRatio'
plotHaplotypeFraction: no visible binding for global variable
  'HaplotypeRatio.2'
plotHaplotypeFraction: no visible binding for global variable 'Chr'
plotHaplotypeFraction: no visible binding for global variable
  'TITANcall'
plotHaplotypeFraction: no visible global function definition for 'par'
plotHaplotypeFraction: no visible global function definition for
  'points'
plotHaplotypeFraction: no visible binding for global variable
  'AllelicRatio'
plotHaplotypeFraction: no visible global function definition for
  'lines'
plotIdiogram.hg38: no visible global function definition for 'par'
plotIdiogram.hg38: no visible binding for global variable 'lsegments'
plotIdiogram.hg38: no visible binding for global variable 'lpolygon'
plotIdiogram.hg38: no visible global function definition for 'axis'
plotIdiogram.hg38: no visible global function definition for 'text'
plotSegmentMedians: no visible binding for global variable 'Chromosome'
plotSegmentMedians: no visible binding for global variable 'TITAN_call'
plotSegmentMedians: no visible global function definition for 'par'
plotSegmentMedians: no visible binding for global variable
  'End_Position.bp.'
plotSegmentMedians: no visible global function definition for '.'
plotSegmentMedians: no visible binding for global variable
  'Start_Position.bp.'
plotSegmentMedians: no visible binding for global variable 'MajorCN'
plotSegmentMedians: no visible binding for global variable 'MinorCN'
plotSegmentMedians : <anonymous>: no visible global function definition
  for 'lines'
plotSegmentMedians: no visible global function definition for 'lines'
plotSegmentMedians: no visible binding for global variable
  'Copy_Number'
plotSubcloneProfiles: no visible binding for global variable 'Chr'
plotSubcloneProfiles: no visible global function definition for 'par'
plotSubcloneProfiles: no visible binding for global variable
  'CopyNumber'
plotSubcloneProfiles: no visible global function definition for 'axis'
plotSubcloneProfiles: no visible global function definition for
  'points'
plotSubcloneProfiles: no visible global function definition for 'mtext'
plotSubcloneProfiles: no visible global function definition for 'lines'
printSDbw: no visible global function definition for 'write.table'
removeCentromereSegs: no visible binding for global variable
  'Chromosome'
removeCentromereSegs: no visible binding for global variable 'Start'
removeCentromereSegs: no visible binding for global variable 'End'
removeEmptyClusters: no visible global function definition for 'tail'
runEMclonalCN: no visible binding for global variable 'head'
updateParameters: no visible global function definition for 'uniroot'
wigToRangedData: no visible global function definition for 'RangedData'
Undefined global functions or variables:
  . Allele.1 Allele.2 AllelicRatio BX BXcounts BamFile BcfFile
  CellularPrevalence Cellular_Prevalence Chr Chromosome ClonalCluster
  CopyNumber Copy_Number Corrected_Call Corrected_Copy_Number
  Corrected_MajorCN Corrected_MinorCN Corrected_Ratio DataFrame End
  End.snp End_Position.bp. HaplotypeBinDepth.mean HaplotypeBinDepth.sum
  HaplotypeDepth.mean HaplotypeDepth.mean.symmetric HaplotypeDepth.sum
  HaplotypeDepth.sum.symmetric HaplotypeFraction
  HaplotypeFraction.symmetric HaplotypeRatio HaplotypeRatio.1
  HaplotypeRatio.2 Length.snp. LogRatio MajorCN Median_HaplotypeRatio
  Median_Ratio Median_logR MinorCN PileupParam RangedData SNPs Sample
  ScanBamParam Start Start.snp Start.telo Start_Position.bp. TITAN_call
  TITANcall abline approxfun as axis depth dunif excludeCentromere
  filterByTargetedSequences haplotypeBin head lines loess
  logR_Copy_Number lowess lpolygon lsegments mtext na.omit nonRef par
  phaseSet phaseSet.aggr phasedAlleleFraction phasedCount
  phasedCount.haploSymmetric pileup points predict queryHits read.delim
  rowRanges rowRanges<- scanBamFlag scanBcf seq.info subjectHits tail
  text tumDepth uniroot unstrsplit write.table
Consider adding
  importFrom("graphics", "abline", "axis", "lines", "mtext", "par",
             "points", "text")
  importFrom("methods", "as")
  importFrom("stats", "approxfun", "dunif", "loess", "lowess", "na.omit",
             "predict", "uniroot")
  importFrom("utils", "head", "read.delim", "tail", "write.table")
to your NAMESPACE file (and ensure that your DESCRIPTION Imports field
contains 'methods').
* checking Rd files ... NOTE
prepare_Rd: correctCN.Rd:51-53: Dropping empty section \details
* checking Rd metadata ... OK
* checking Rd cross-references ... NOTE
Package unavailable to check Rd xrefs: 'list'
* checking for missing documentation entries ... WARNING
Undocumented code objects:
  'plotIdiogram.hg38'
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 line endings in C/C++/Fortran sources/headers ... OK
* checking compiled code ... NOTE
Note: information on .o files for i386 is not available
Note: information on .o files for x64 is not available
File 'C:/Users/biocbuild/bbs-3.14-bioc/R/library/TitanCNA/libs/i386/TitanCNA.dll':
  Found 'abort', possibly from 'abort' (C), 'runtime' (Fortran)
File 'C:/Users/biocbuild/bbs-3.14-bioc/R/library/TitanCNA/libs/x64/TitanCNA.dll':
  Found 'abort', possibly from 'abort' (C), 'runtime' (Fortran)

Compiled code should not call entry points which might terminate R nor
write to stdout/stderr instead of to the console, nor use Fortran I/O
nor system RNGs. The detected symbols are linked into the code but
might come from libraries and not actually be called.

See 'Writing portable packages' in the 'Writing R Extensions' manual.
* 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
TitanCNA-package   33.27   0.91   34.49
runEMclonalCN      23.49   0.25   23.73
filterData          8.48   0.21    8.68
TitanCNA-plotting   8.53   0.11    8.64
getPositionOverlap  7.53   0.26    7.80
correctReadDepth    6.72   0.17    6.89
computeSDbwIndex    6.16   0.08    6.24
** running examples for arch 'x64' ... OK
Examples with CPU (user + system) or elapsed time > 5s
                    user system elapsed
TitanCNA-package   34.50   0.66   35.16
runEMclonalCN      23.54   0.27   23.80
filterData          9.38   0.04    9.42
TitanCNA-plotting   8.70   0.13    8.82
getPositionOverlap  7.34   0.11    7.45
computeSDbwIndex    6.50   0.00    6.50
correctReadDepth    5.91   0.13    6.04
* 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, 5 NOTEs
See
  'C:/Users/biocbuild/bbs-3.14-bioc/meat/TitanCNA.Rcheck/00check.log'
for details.



Installation output

TitanCNA.Rcheck/00install.out

##############################################################################
##############################################################################
###
### Running command:
###
###   C:\cygwin\bin\curl.exe -O http://155.52.207.166/BBS/3.14/bioc/src/contrib/TitanCNA_1.32.0.tar.gz && rm -rf TitanCNA.buildbin-libdir && mkdir TitanCNA.buildbin-libdir && C:\Users\biocbuild\bbs-3.14-bioc\R\bin\R.exe CMD INSTALL --merge-multiarch --build --library=TitanCNA.buildbin-libdir TitanCNA_1.32.0.tar.gz && C:\Users\biocbuild\bbs-3.14-bioc\R\bin\R.exe CMD INSTALL TitanCNA_1.32.0.zip && rm TitanCNA_1.32.0.tar.gz TitanCNA_1.32.0.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
 99 5041k   99 5020k    0     0  5483k      0 --:--:-- --:--:-- --:--:-- 5486k
100 5041k  100 5041k    0     0  5499k      0 --:--:-- --:--:-- --:--:-- 5498k

install for i386

* installing *source* package 'TitanCNA' ...
** using staged installation
** libs
"C:/rtools40/mingw32/bin/"gcc  -I"C:/Users/BIOCBU~1/BBS-3~1.14-/R/include" -DNDEBUG     -I"C:/extsoft/include"     -O2 -Wall  -std=gnu99 -mfpmath=sse -msse2 -mstackrealign  -c fwd_backC_clonalCN.c -o fwd_backC_clonalCN.o
"C:/rtools40/mingw32/bin/"gcc  -I"C:/Users/BIOCBU~1/BBS-3~1.14-/R/include" -DNDEBUG     -I"C:/extsoft/include"     -O2 -Wall  -std=gnu99 -mfpmath=sse -msse2 -mstackrealign  -c getPositionOverlapC.c -o getPositionOverlapC.o
"C:/rtools40/mingw32/bin/"gcc  -I"C:/Users/BIOCBU~1/BBS-3~1.14-/R/include" -DNDEBUG     -I"C:/extsoft/include"     -O2 -Wall  -std=gnu99 -mfpmath=sse -msse2 -mstackrealign  -c register.c -o register.o
"C:/rtools40/mingw32/bin/"gcc  -I"C:/Users/BIOCBU~1/BBS-3~1.14-/R/include" -DNDEBUG     -I"C:/extsoft/include"     -O2 -Wall  -std=gnu99 -mfpmath=sse -msse2 -mstackrealign  -c viterbiC_clonalCN.c -o viterbiC_clonalCN.o
C:/rtools40/mingw32/bin/gcc -shared -s -static-libgcc -o TitanCNA.dll tmp.def fwd_backC_clonalCN.o getPositionOverlapC.o register.o viterbiC_clonalCN.o -LC:/extsoft/lib/i386 -LC:/extsoft/lib -LC:/Users/BIOCBU~1/BBS-3~1.14-/R/bin/i386 -lR
installing to C:/Users/biocbuild/bbs-3.14-bioc/meat/TitanCNA.buildbin-libdir/00LOCK-TitanCNA/00new/TitanCNA/libs/i386
** R
** data
** inst
** byte-compile and prepare package for lazy loading
Warning: replacing previous import 'GenomicRanges::shift' by 'data.table::shift' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::collapse' by 'dplyr::collapse' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::last' by 'dplyr::last' when loading 'TitanCNA'
Warning: replacing previous import 'GenomicRanges::union' by 'dplyr::union' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::slice' by 'dplyr::slice' when loading 'TitanCNA'
Warning: replacing previous import 'GenomeInfoDb::intersect' by 'dplyr::intersect' when loading 'TitanCNA'
Warning: replacing previous import 'GenomicRanges::setdiff' by 'dplyr::setdiff' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::first' by 'dplyr::first' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::desc' by 'dplyr::desc' when loading 'TitanCNA'
Warning: replacing previous import 'BiocGenerics::combine' by 'dplyr::combine' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::between' by 'dplyr::between' when loading 'TitanCNA'
Warning: replacing previous import 'dplyr::select' by 'VariantAnnotation::select' when loading 'TitanCNA'
** help
*** installing help indices
  converting help for package 'TitanCNA'
    finding HTML links ... done
    TitanCNA-dataset                        html  
    TitanCNA-output                         html  
    TitanCNA-package                        html  
    TitanCNA-plotting                       html  
    computeSDbwIndex                        html  
    correctCN                               html  
    correctReadDepth                        html  
    filterData                              html  
    getPositionOverlap                      html  
    haplotype                               html  
    loadAlleleCounts                        html  
    loadDefaultParameters                   html  
    runEMclonalCN                           html  
    finding level-2 HTML links ... done

    viterbiClonalCN                         html  
    wigImport                               html  
** building package indices
** installing vignettes
** testing if installed package can be loaded from temporary location
Warning: replacing previous import 'GenomicRanges::shift' by 'data.table::shift' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::collapse' by 'dplyr::collapse' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::last' by 'dplyr::last' when loading 'TitanCNA'
Warning: replacing previous import 'GenomicRanges::union' by 'dplyr::union' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::slice' by 'dplyr::slice' when loading 'TitanCNA'
Warning: replacing previous import 'GenomeInfoDb::intersect' by 'dplyr::intersect' when loading 'TitanCNA'
Warning: replacing previous import 'GenomicRanges::setdiff' by 'dplyr::setdiff' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::first' by 'dplyr::first' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::desc' by 'dplyr::desc' when loading 'TitanCNA'
Warning: replacing previous import 'BiocGenerics::combine' by 'dplyr::combine' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::between' by 'dplyr::between' when loading 'TitanCNA'
Warning: replacing previous import 'dplyr::select' by 'VariantAnnotation::select' when loading 'TitanCNA'
** testing if installed package can be loaded from final location
Warning: replacing previous import 'GenomicRanges::shift' by 'data.table::shift' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::collapse' by 'dplyr::collapse' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::last' by 'dplyr::last' when loading 'TitanCNA'
Warning: replacing previous import 'GenomicRanges::union' by 'dplyr::union' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::slice' by 'dplyr::slice' when loading 'TitanCNA'
Warning: replacing previous import 'GenomeInfoDb::intersect' by 'dplyr::intersect' when loading 'TitanCNA'
Warning: replacing previous import 'GenomicRanges::setdiff' by 'dplyr::setdiff' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::first' by 'dplyr::first' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::desc' by 'dplyr::desc' when loading 'TitanCNA'
Warning: replacing previous import 'BiocGenerics::combine' by 'dplyr::combine' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::between' by 'dplyr::between' when loading 'TitanCNA'
Warning: replacing previous import 'dplyr::select' by 'VariantAnnotation::select' when loading 'TitanCNA'
** testing if installed package keeps a record of temporary installation path

install for x64

* installing *source* package 'TitanCNA' ...
** libs
"C:/rtools40/mingw64/bin/"gcc  -I"C:/Users/BIOCBU~1/BBS-3~1.14-/R/include" -DNDEBUG     -I"C:/extsoft/include"     -O2 -Wall  -std=gnu99 -mfpmath=sse -msse2 -mstackrealign  -c fwd_backC_clonalCN.c -o fwd_backC_clonalCN.o
"C:/rtools40/mingw64/bin/"gcc  -I"C:/Users/BIOCBU~1/BBS-3~1.14-/R/include" -DNDEBUG     -I"C:/extsoft/include"     -O2 -Wall  -std=gnu99 -mfpmath=sse -msse2 -mstackrealign  -c getPositionOverlapC.c -o getPositionOverlapC.o
"C:/rtools40/mingw64/bin/"gcc  -I"C:/Users/BIOCBU~1/BBS-3~1.14-/R/include" -DNDEBUG     -I"C:/extsoft/include"     -O2 -Wall  -std=gnu99 -mfpmath=sse -msse2 -mstackrealign  -c register.c -o register.o
"C:/rtools40/mingw64/bin/"gcc  -I"C:/Users/BIOCBU~1/BBS-3~1.14-/R/include" -DNDEBUG     -I"C:/extsoft/include"     -O2 -Wall  -std=gnu99 -mfpmath=sse -msse2 -mstackrealign  -c viterbiC_clonalCN.c -o viterbiC_clonalCN.o
C:/rtools40/mingw64/bin/gcc -shared -s -static-libgcc -o TitanCNA.dll tmp.def fwd_backC_clonalCN.o getPositionOverlapC.o register.o viterbiC_clonalCN.o -LC:/extsoft/lib/x64 -LC:/extsoft/lib -LC:/Users/BIOCBU~1/BBS-3~1.14-/R/bin/x64 -lR
installing to C:/Users/biocbuild/bbs-3.14-bioc/meat/TitanCNA.buildbin-libdir/TitanCNA/libs/x64
** testing if installed package can be loaded
Warning: replacing previous import 'GenomicRanges::shift' by 'data.table::shift' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::collapse' by 'dplyr::collapse' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::last' by 'dplyr::last' when loading 'TitanCNA'
Warning: replacing previous import 'GenomicRanges::union' by 'dplyr::union' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::slice' by 'dplyr::slice' when loading 'TitanCNA'
Warning: replacing previous import 'GenomeInfoDb::intersect' by 'dplyr::intersect' when loading 'TitanCNA'
Warning: replacing previous import 'GenomicRanges::setdiff' by 'dplyr::setdiff' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::first' by 'dplyr::first' when loading 'TitanCNA'
Warning: replacing previous import 'IRanges::desc' by 'dplyr::desc' when loading 'TitanCNA'
Warning: replacing previous import 'BiocGenerics::combine' by 'dplyr::combine' when loading 'TitanCNA'
Warning: replacing previous import 'data.table::between' by 'dplyr::between' when loading 'TitanCNA'
Warning: replacing previous import 'dplyr::select' by 'VariantAnnotation::select' when loading 'TitanCNA'
* MD5 sums
packaged installation of 'TitanCNA' as TitanCNA_1.32.0.zip
* DONE (TitanCNA)
* installing to library 'C:/Users/biocbuild/bbs-3.14-bioc/R/library'
package 'TitanCNA' successfully unpacked and MD5 sums checked

Tests output


Example timings

TitanCNA.Rcheck/examples_i386/TitanCNA-Ex.timings

nameusersystemelapsed
TitanCNA-output1.940.142.09
TitanCNA-package33.27 0.9134.49
TitanCNA-plotting8.530.118.64
computeSDbwIndex6.160.086.24
correctCN0.860.010.89
correctReadDepth6.720.176.89
filterData8.480.218.68
getPositionOverlap7.530.267.80
haplotype000
loadAlleleCounts0.640.330.97
loadDefaultParameters000
runEMclonalCN23.49 0.2523.73
viterbiClonalCN0.590.000.60
wigImport0.20.00.2

TitanCNA.Rcheck/examples_x64/TitanCNA-Ex.timings

nameusersystemelapsed
TitanCNA-output2.070.022.18
TitanCNA-package34.50 0.6635.16
TitanCNA-plotting8.700.138.82
computeSDbwIndex6.50.06.5
correctCN0.870.010.89
correctReadDepth5.910.136.04
filterData9.380.049.42
getPositionOverlap7.340.117.45
haplotype000
loadAlleleCounts0.760.080.84
loadDefaultParameters000
runEMclonalCN23.54 0.2723.80
viterbiClonalCN0.530.000.53
wigImport0.140.000.14