seqCNA

DOI: 10.18129/B9.bioc.seqCNA    

Copy number analysis of high-throughput sequencing cancer data

Bioconductor version: Release (3.6)

Copy number analysis of high-throughput sequencing cancer data with fast summarization, extensive filtering and improved normalization

Author: David Mosen-Ansorena

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

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

Installation

To install this package, start R and enter:

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

Documentation

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

browseVignettes("seqCNA")

 

PDF R Script seqCNA
PDF   Reference Manual

Details

biocViews CopyNumberVariation, Genetics, Sequencing, Software
Version 1.24.0
In Bioconductor since BioC 2.13 (R-3.0) (4.5 years)
License GPL-3
Depends R (>= 3.0), GLAD(>= 2.14), doSNOW (>= 1.0.5), adehabitatLT (>= 0.3.4), seqCNA.annot(>= 0.99), methods
Imports
LinkingTo
Suggests
SystemRequirements samtools
Enhances
URL
Depends On Me
Imports Me
Suggests Me
Build Report  

Package Archives

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

Source Package seqCNA_1.24.0.tar.gz
Windows Binary seqCNA_1.24.0.zip (32- & 64-bit)
Mac OS X 10.11 (El Capitan) seqCNA_1.24.0.tgz
Source Repository git clone https://git.bioconductor.org/packages/seqCNA
Package Short Url http://bioconductor.org/packages/seqCNA/
Package Downloads Report Download Stats

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