Last data update: 2014.03.03
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PureCN
Package: PureCN
Type: Package
Title: Estimating tumor purity, ploidy, LOH, and SNV status using
hybrid capture NGS data
Version: 1.0.3
Date: 2016-06-04
Author: Markus Riester
Maintainer: Markus Riester <markus.riester@novartis.com>
Description: This package estimates tumor purity, copy number, loss of
heterozygosity (LOH), and status of single nucleotide variants (SNVs).
PureCN is designed for hybrid capture sequencing data, integrates
well with standard somatic variant detection pipelines,
and has support for tumor samples without matching normal samples.
Depends: R (>= 3.3), DNAcopy, VariantAnnotation (>= 1.14.1)
Imports: GenomicRanges (>= 1.20.3), IRanges (>= 2.2.1), RColorBrewer,
S4Vectors, data.table, grDevices, graphics, stats, utils,
SummarizedExperiment, GenomeInfoDb
Suggests: PSCBS, RUnit, BiocStyle, BiocGenerics, knitr
VignetteBuilder: knitr
License: Artistic-2.0
biocViews: CopyNumberVariation, Software, Sequencing,
VariantAnnotation, VariantDetection
NeedsCompilation: no
Packaged: 2016-06-06 06:04:50 UTC; biocbuild
Install log
* installing to library '/home/ddbj/local/lib64/R/library'
* installing *source* package 'PureCN' ...
** R
** data
** inst
** preparing package for lazy loading
** help
*** installing help indices
converting help for package 'PureCN'
finding HTML links ... done
chr.hash html
correctCoverageBias html
createCurationFile html
createExonWeightFile html
createNormalDatabase html
createSNPBlacklist html
filterVcfBasic html
filterVcfMuTect html
findBestNormal html
findFocal html
getSexFromCoverage html
plotAbs html
plotBestNormal html
poolCoverage html
predictSomatic html
purecn.example.output html
readCoverageGatk html
readCurationFile html
runAbsoluteCN html
segmentationCBS html
segmentationPSCBS html
setPriorVcf html
** building package indices
** installing vignettes
** testing if installed package can be loaded
* DONE (PureCN)
Making 'packages.html' ... done
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