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

seqCNA.annot

Annotation for the copy number analysis of deep sequencing cancer data with seqCNA

Bioconductor version: 2.13

Provides annotation on GC content, mappability and genomic features for various genomes

Author: David Mosen-Ansorena

Maintainer: David Mosen-Ansorena <dmosen.gn at cicbiogune.es>

Installation

To install this package, start R and enter:

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

Documentation

To view documentation for the version of this package installed in your system, start R and enter:

browseVignettes("seqCNA.annot")

 

PDF		Reference Manual

Details

biocViews	Bioinformatics, CopyNumberVariants, ExperimentData, Genetics, HighThroughputSequencing
Version	0.99.1
License	GPL-3
Depends	R (>= 2.10)
Imports
Suggests
System Requirements
URL
Depends On Me	seqCNA
Imports Me
Suggests Me

Package Archives

Follow Installation instructions to use this package in your R session.

Package Source	seqCNA.annot_0.99.1.tar.gz
Windows Binary	seqCNA.annot_0.99.1.zip (32- & 64-bit)
Mac OS X 10.6 (Snow Leopard)	seqCNA.annot_0.99.1.tgz
Browse/checkout source	(username/password: readonly)
Package Downloads Report	Download Stats