Back to the "Multiple platform build/check report" A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S [T] U  V  W  X  Y  Z 

BioC 3.6: CHECK report for TitanCNA on veracruz1

This page was generated on 2017-08-16 13:45:16 -0400 (Wed, 16 Aug 2017).

Package 1345/1410HostnameOS / ArchINSTALLBUILDCHECKBUILD BIN
TitanCNA 1.15.0
Gavin Ha , Sohrab P Shah
Snapshot Date: 2017-08-15 17:18:21 -0400 (Tue, 15 Aug 2017)
URL: https://hedgehog.fhcrc.org/bioconductor/trunk/madman/Rpacks/TitanCNA
Last Changed Rev: 131890 / Revision: 131943
Last Changed Date: 2017-08-10 14:55:44 -0400 (Thu, 10 Aug 2017)
malbec1 Linux (Ubuntu 16.04.1 LTS) / x86_64  NotNeeded  OK  ERROR 
tokay1 Windows Server 2012 R2 Standard / x64  NotNeeded  OK  ERROR  OK 
veracruz1 OS X 10.11.6 El Capitan / x86_64  NotNeeded  OK [ ERROR ] OK 

Summary

Package: TitanCNA
Version: 1.15.0
Command: /Library/Frameworks/R.framework/Versions/Current/Resources/bin/R CMD check --no-vignettes --timings TitanCNA_1.15.0.tar.gz
StartedAt: 2017-08-16 09:09:59 -0400 (Wed, 16 Aug 2017)
EndedAt: 2017-08-16 09:15:14 -0400 (Wed, 16 Aug 2017)
EllapsedTime: 315.6 seconds
RetCode: 1
Status:  ERROR 
CheckDir: TitanCNA.Rcheck
Warnings: NA

Command output

##############################################################################
##############################################################################
###
### Running command:
###
###   /Library/Frameworks/R.framework/Versions/Current/Resources/bin/R CMD check --no-vignettes --timings TitanCNA_1.15.0.tar.gz
###
##############################################################################
##############################################################################


* using log directory ‘/Users/biocbuild/bbs-3.6-bioc/meat/TitanCNA.Rcheck’
* using R version 3.4.1 (2017-06-30)
* using platform: x86_64-apple-darwin15.6.0 (64-bit)
* using session charset: UTF-8
* using option ‘--no-vignettes’
* checking for file ‘TitanCNA/DESCRIPTION’ ... OK
* checking extension type ... Package
* this is package ‘TitanCNA’ version ‘1.15.0’
* 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 ‘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 ‘data.table::first’ by ‘dplyr::first’ when loading ‘TitanCNA’
  Warning: replacing previous import ‘IRanges::slice’ by ‘dplyr::slice’ when loading ‘TitanCNA’
  Warning: replacing previous import ‘data.table::between’ by ‘dplyr::between’ when loading ‘TitanCNA’
  Warning: replacing previous import ‘IRanges::collapse’ by ‘dplyr::collapse’ when loading ‘TitanCNA’
  Warning: replacing previous import ‘GenomeInfoDb::intersect’ by ‘dplyr::intersect’ when loading ‘TitanCNA’
  Warning: replacing previous import ‘data.table::last’ by ‘dplyr::last’ when loading ‘TitanCNA’
  Warning: replacing previous import ‘GenomicRanges::setdiff’ by ‘dplyr::setdiff’ when loading ‘TitanCNA’
  Warning: replacing previous import ‘GenomicRanges::union’ by ‘dplyr::union’ when loading ‘TitanCNA’
  Warning: replacing previous import ‘IRanges::desc’ by ‘dplyr::desc’ when loading ‘TitanCNA’
  Warning: replacing previous import ‘dplyr::select’ by ‘VariantAnnotation::select’ when loading ‘TitanCNA’
See ‘/Users/biocbuild/bbs-3.6-bioc/meat/TitanCNA.Rcheck/00install.out’ for details.
* checking installed package size ... NOTE
  installed size is  7.5Mb
  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
* 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 loading without being on the library search path ... 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 ‘CopyNumber’
computeSDbwIndex: no visible binding for global variable
  ‘ClonalCluster’
computeSDbwIndex: no visible binding for global variable ‘TITANstate’
computeSDbwIndex: no visible binding for global variable ‘TITANcall’
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 ‘Chr’
correctIntegerCN: no visible binding for global variable ‘LogRatio’
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 ‘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
  ‘xtabs’
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’
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
  ‘keepChr’
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
  ‘keepChr’
loadReadCountsFromBed: no visible global function definition for
  ‘excludeCentromere’
loadReadCountsFromBed: no visible global function definition for
  ‘filterByTargetedSequences’
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 global function definition for ‘plot’
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 global function definition for ‘plot’
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 ‘plot’
plotCNlogRByChr: no visible binding for global variable ‘CopyNumber’
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.’
plotCNlogRByChr: no visible binding for global variable ‘Copy_Number’
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 ‘plot’
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 global function definition for ‘par’
plotHaplotypeFraction: no visible global function definition for ‘plot’
plotHaplotypeFraction: no visible global function definition for
  ‘points’
plotHaplotypeFraction: no visible binding for global variable
  ‘AllelicRatio’
plotHaplotypeFraction: no visible global function definition for
  ‘lines’
plotHaplotypeFraction: no visible binding for global variable
  ‘TITANcall’
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: no visible binding for global variable
  ‘Copy_Number’
plotSegmentMedians: no visible global function definition for ‘plot’
plotSegmentMedians : <anonymous>: no visible global function definition
  for ‘lines’
plotSegmentMedians: no visible global function definition for ‘lines’
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 ‘plot’
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’
Undefined global functions or variables:
  . Allele.1 Allele.2 AllelicRatio BX BXcounts CellularPrevalence Chr
  Chromosome ClonalCluster CopyNumber Copy_Number Corrected_Call
  Corrected_Copy_Number 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 LogRatio MajorCN Median_logR MinorCN SNPs Sample
  Start Start.snp Start.telo Start_Position.bp. TITAN_call TITANcall
  TITANstate abline approxfun as axis depth dunif excludeCentromere
  filterByTargetedSequences haplotypeBin head keepChr lines loess
  logR_Copy_Number lowess mtext na.omit nonRef par phaseSet
  phaseSet.aggr phasedAlleleFraction phasedCount
  phasedCount.haploSymmetric plot points predict queryHits read.delim
  rowRanges rowRanges<- seq.info subjectHits tail tumDepth uniroot
  unstrsplit write.table xtabs
Consider adding
  importFrom("graphics", "abline", "axis", "lines", "mtext", "par",
             "plot", "points")
  importFrom("methods", "as")
  importFrom("stats", "approxfun", "dunif", "loess", "lowess", "na.omit",
             "predict", "uniroot", "xtabs")
  importFrom("utils", "head", "read.delim", "tail", "write.table")
to your NAMESPACE file (and ensure that your DESCRIPTION Imports field
contains 'methods').
* checking Rd files ... OK
* checking Rd metadata ... OK
* checking Rd cross-references ... NOTE
Package unavailable to check Rd xrefs: ‘list’
* checking for missing documentation entries ... OK
* checking for code/documentation mismatches ... WARNING
Codoc mismatches from documentation object 'output-methods':
outputTitanResults
  Code: function(data, convergeParams, optimalPath, filename = NULL,
                 is.haplotypeData = FALSE, posteriorProbs = FALSE,
                 subcloneProfiles = TRUE, correctResults = TRUE,
                 proportionThreshold = 0.05, proportionThresholdClonal
                 = 0.05, recomputeLogLik = TRUE, rerunViterbi = FALSE,
                 verbose = TRUE)
  Docs: function(data, convergeParams, optimalPath, filename = NULL,
                 is.haplotypeData = FALSE, posteriorProbs = FALSE,
                 subcloneProfiles = TRUE, correctResults = TRUE,
                 proportionThreshold = 0.05, proportionThresholdClonal
                 = 0.05, verbose = TRUE)
  Argument names in code not in docs:
    recomputeLogLik rerunViterbi
  Mismatches in argument names:
    Position: 11 Code: recomputeLogLik Docs: verbose

Codoc mismatches from documentation object 'removeEmptyClusters':
removeEmptyClusters
  Code: function(data, convergeParams, results, proportionThreshold =
                 0.001, proportionThresholdClonal = 0.05,
                 recomputeLogLik = TRUE, verbose = TRUE)
  Docs: function(convergeParams, results, proportionThreshold = 0.001,
                 proportionThresholdClonal = 0.05)
  Argument names in code not in docs:
    data recomputeLogLik verbose
  Mismatches in argument names (first 3):
    Position: 1 Code: data Docs: convergeParams
    Position: 2 Code: convergeParams Docs: results
    Position: 3 Code: results Docs: proportionThreshold

* 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 ... OK
* checking sizes of PDF files under ‘inst/doc’ ... OK
* checking installed files from ‘inst/doc’ ... OK
* checking files in ‘vignettes’ ... OK
* checking examples ... ERROR
Running examples in ‘TitanCNA-Ex.R’ failed
The error most likely occurred in:

> base::assign(".ptime", proc.time(), pos = "CheckExEnv")
> ### Name: removeEmptyClusters
> ### Title: Post-process TitanCNA results by removing clusters with
> ###   proportion of data points altered lower than a threshold.  The number
> ###   of clonal clusters, cellular prevalence, and normal contamination
> ###   will be adjusted to reflect the remaining clonal clusters.
> ### Aliases: removeEmptyClusters
> ### Keywords: manip
> 
> ### ** Examples
> 
> data(EMresults)
> 
> #### COMPUTE OPTIMAL STATE PATH USING VITERBI ####
> optimalPath <- viterbiClonalCN(data, convergeParams)
> 
> #### FORMAT RESULTS ####
> results <- outputTitanResults(data, convergeParams, optimalPath, 
+                               filename = NULL, posteriorProbs = FALSE,
+                               subcloneProfiles = TRUE)
outputTitanResults: Correcting results...
outputTitanResults: Recomputing log-likelihood.
titan: Running HMM...
fwdBack: Iteration 1 chr: 1 
Using Coordinate Descent iteration 11 with Fval=-22824 and n=0.2643 (fixed), s=[0.00,0.55], phi=1.571
fwdBack: loglik=-34034.1335
fwdBack: priorN=0.0000
fwdBack: priorS=0.0000
fwdBack: priorVar=-793.5800
fwdBack: priorVarR=0.0000
fwdBack: priorPhi=0.0000
fwdBack: priorPiG=30.5572
fwdBack: priorPiZ=0.9808
fwdBack: EM iteration 1 complete loglik=-34796.1754
fwdBack: Elapsed time for iteration 1: 0.0360m
fwdBack: Total elapsed time: 0.0589m
> 
> #### REMOVE EMPTY CLONAL CLUSTERS ####
> corrResults <- removeEmptyClusters(convergeParams, results, proportionThreshold = 0.001,
+ 																		proportionThresholdClonal = 0.3)
Error in removeEmptyClusters(convergeParams, results, proportionThreshold = 0.001,  : 
  could not find function "removeEmptyClusters"
Execution halted
* 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 ERROR, 2 WARNINGs, 3 NOTEs
See
  ‘/Users/biocbuild/bbs-3.6-bioc/meat/TitanCNA.Rcheck/00check.log’
for details.

TitanCNA.Rcheck/00install.out:

* installing *source* package ‘TitanCNA’ ...
** libs
clang -I/Library/Frameworks/R.framework/Resources/include -DNDEBUG   -I/usr/local/include   -fPIC  -Wall -g -O2  -c fwd_backC_clonalCN.c -o fwd_backC_clonalCN.o
fwd_backC_clonalCN.c:257:21: warning: equality comparison with extraneous parentheses [-Wparentheses-equality]
            if ((iZS==jZS)){
                 ˜˜˜^˜˜˜˜
fwd_backC_clonalCN.c:257:21: note: remove extraneous parentheses around the comparison to silence this warning
            if ((iZS==jZS)){
                ˜   ^    ˜
fwd_backC_clonalCN.c:257:21: note: use '=' to turn this equality comparison into an assignment
            if ((iZS==jZS)){
                    ^˜
                    =
1 warning generated.
clang -I/Library/Frameworks/R.framework/Resources/include -DNDEBUG   -I/usr/local/include   -fPIC  -Wall -g -O2  -c getPositionOverlapC.c -o getPositionOverlapC.o
clang -I/Library/Frameworks/R.framework/Resources/include -DNDEBUG   -I/usr/local/include   -fPIC  -Wall -g -O2  -c register.c -o register.o
clang -I/Library/Frameworks/R.framework/Resources/include -DNDEBUG   -I/usr/local/include   -fPIC  -Wall -g -O2  -c viterbiC_clonalCN.c -o viterbiC_clonalCN.o
clang -dynamiclib -Wl,-headerpad_max_install_names -undefined dynamic_lookup -single_module -multiply_defined suppress -L/Library/Frameworks/R.framework/Resources/lib -L/usr/local/lib -o TitanCNA.so fwd_backC_clonalCN.o getPositionOverlapC.o register.o viterbiC_clonalCN.o -F/Library/Frameworks/R.framework/.. -framework R -Wl,-framework -Wl,CoreFoundation
installing to /Users/biocbuild/bbs-3.6-bioc/meat/TitanCNA.Rcheck/TitanCNA/libs
** R
** data
** inst
** preparing package for lazy loading
Warning: replacing previous import ‘GenomicRanges::shift’ by ‘data.table::shift’ when loading ‘TitanCNA’
Warning: replacing previous import ‘data.table::first’ by ‘dplyr::first’ when loading ‘TitanCNA’
Warning: replacing previous import ‘IRanges::slice’ by ‘dplyr::slice’ when loading ‘TitanCNA’
Warning: replacing previous import ‘data.table::between’ by ‘dplyr::between’ when loading ‘TitanCNA’
Warning: replacing previous import ‘IRanges::collapse’ by ‘dplyr::collapse’ when loading ‘TitanCNA’
Warning: replacing previous import ‘GenomeInfoDb::intersect’ by ‘dplyr::intersect’ when loading ‘TitanCNA’
Warning: replacing previous import ‘data.table::last’ by ‘dplyr::last’ when loading ‘TitanCNA’
Warning: replacing previous import ‘GenomicRanges::setdiff’ by ‘dplyr::setdiff’ when loading ‘TitanCNA’
Warning: replacing previous import ‘GenomicRanges::union’ by ‘dplyr::union’ when loading ‘TitanCNA’
Warning: replacing previous import ‘IRanges::desc’ by ‘dplyr::desc’ when loading ‘TitanCNA’
Warning: replacing previous import ‘dplyr::select’ by ‘VariantAnnotation::select’ when loading ‘TitanCNA’
** help
*** installing help indices
** building package indices
** installing vignettes
** testing if installed package can be loaded
Warning: replacing previous import ‘GenomicRanges::shift’ by ‘data.table::shift’ when loading ‘TitanCNA’
Warning: replacing previous import ‘data.table::first’ by ‘dplyr::first’ when loading ‘TitanCNA’
Warning: replacing previous import ‘IRanges::slice’ by ‘dplyr::slice’ when loading ‘TitanCNA’
Warning: replacing previous import ‘data.table::between’ by ‘dplyr::between’ when loading ‘TitanCNA’
Warning: replacing previous import ‘IRanges::collapse’ by ‘dplyr::collapse’ when loading ‘TitanCNA’
Warning: replacing previous import ‘GenomeInfoDb::intersect’ by ‘dplyr::intersect’ when loading ‘TitanCNA’
Warning: replacing previous import ‘data.table::last’ by ‘dplyr::last’ when loading ‘TitanCNA’
Warning: replacing previous import ‘GenomicRanges::setdiff’ by ‘dplyr::setdiff’ when loading ‘TitanCNA’
Warning: replacing previous import ‘GenomicRanges::union’ by ‘dplyr::union’ when loading ‘TitanCNA’
Warning: replacing previous import ‘IRanges::desc’ by ‘dplyr::desc’ when loading ‘TitanCNA’
Warning: replacing previous import ‘dplyr::select’ by ‘VariantAnnotation::select’ when loading ‘TitanCNA’
* DONE (TitanCNA)

TitanCNA.Rcheck/TitanCNA-Ex.timings:

nameusersystemelapsed
TitanCNA-output5.3860.0815.613
TitanCNA-package27.624 0.39328.695
TitanCNA-plotting5.4570.0455.590
computeSDbwIndex3.7740.0183.869
correctReadDepth9.1640.2649.696
extractAlleleReadCounts000
filterData 9.454 0.35110.104
getPositionOverlap9.2490.3289.868
haplotype0.0010.0000.001
loadAlleleCounts0.7950.0210.843
loadDefaultParameters0.1030.0020.106