To install this package, start R and enter:

## try http:// if https:// URLs are not supported
source("https://bioconductor.org/biocLite.R")
biocLite("seqCNA.annot")

In most cases, you don't need to download the package archive at all.

seqCNA.annot

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

Bioconductor version: Release (3.4)

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>

Citation (from within R, enter citation("seqCNA.annot")):

To install this package, start R and enter:

## try http:// if https:// URLs are not supported
source("https://bioconductor.org/biocLite.R")
biocLite("seqCNA.annot")


PDF		Reference Manual

biocViews	CopyNumberVariationData, ExperimentData, Genome
Version	1.10.0
License	GPL-3
Depends	R (>= 2.10)
Imports
LinkingTo
Suggests
SystemRequirements
Enhances
URL
Depends On Me	seqCNA
Imports Me
Suggests Me
Build Report

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

Package Source	seqCNA.annot_1.10.0.tar.gz
Windows Binary
Mac OS X 10.9 (Mavericks)
Subversion source	(username/password: readonly)
Package Short Url	http://bioconductor.org/packages/seqCNA.annot/
Package Downloads Report	Download Stats

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