HMMcopy

Copy number prediction with correction for GC and mappability bias for HTS data

Bioconductor version: Release (2.11)

Corrects GC and mappability biases for readcounts (i.e. coverage) in non-overlapping windows of fixed length for single whole genome samples, yielding a rough estimate of copy number for furthur analysis. Designed for rapid correction of high coverage whole genome tumour and normal samples.

Author: Daniel Lai, Gavin Ha, Sohrab Shah

Maintainer: Daniel Lai <jujubix at cs.ubc.ca>, Gavin Ha <gha at bccrc.ca>, Sohrab Shah <sshah at bccrc.ca>

To install this package, start R and enter:

    source("http://bioconductor.org/biocLite.R")
    biocLite("HMMcopy")

To cite this package in a publication, start R and enter:

    citation("HMMcopy")

Documentation

PDF R Script HMMcopy
PDF   Reference Manual

Details

biocViews CopyNumberVariants, HighThroughputSequencing, Microarray, Preprocessing, Sequencing, Software, Visualization
Version 1.0.0
In Bioconductor since BioC 2.11 (R-2.15)
License GPL-3
Depends R (>= 2.10.0), IRanges(>= 1.4.16), geneplotter(>= 1.24.0)
Imports
Suggests
System Requirements
URL
Depends On Me
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Package Downloads

Package Source HMMcopy_1.0.0.tar.gz
Windows Binary HMMcopy_1.0.0.zip (32- & 64-bit)
MacOS 10.5 (Leopard) HMMcopy_1.0.0.tgz
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