Bioconductor version: Release (2.12)
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")
    | R Script | HMMcopy | |
| Reference Manual | 
| biocViews | CopyNumberVariants, HighThroughputSequencing, Microarray, Preprocessing, Sequencing, Software, Visualization | 
| Version | 1.2.0 | 
| In Bioconductor since | BioC 2.11 (R-2.16) | 
| License | GPL-3 | 
| Depends | R (>= 2.10.0), IRanges(>= 1.4.16), geneplotter(>= 1.24.0) | 
| Imports | |
| Suggests | |
| System Requirements | |
| URL | |
| Depends On Me | |
| Imports Me | |
| Suggests Me | 
| Package Source | HMMcopy_1.2.0.tar.gz | 
| Windows Binary | HMMcopy_1.2.0.zip (32- & 64-bit) | 
| Mac OS X 10.6 (Snow Leopard) | HMMcopy_1.2.0.tgz | 
| Package Downloads Report | Download Stats | 
 
  
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