Bioconductor version: Release (2.11)
This package is intended to facilitate gene-set association with rare CNVs in case-control studies.
Author: Daniele Merico <daniele.merico at gmail.com>; packaged by Robert Ziman <rziman at gmail.com>
Maintainer: Robert Ziman <rziman at gmail.com>
To install this package, start R and enter:
source("http://bioconductor.org/biocLite.R") biocLite("cnvGSA")
To cite this package in a publication, start R and enter:
citation("cnvGSA")
R Script | cnvGSA - Gene-Set Analysis of Rare Copy Number Variants | |
Reference Manual |
biocViews | MultipleComparisons, Software |
Version | 1.2.0 |
In Bioconductor since | BioC 2.10 (R-2.15) |
License | LGPL |
Depends | methods, brglm |
Imports | |
Suggests | cnvGSAdata, org.Hs.eg.db |
System Requirements | |
URL | |
Depends On Me | cnvGSAdata |
Imports Me | |
Suggests Me |
Package Source | cnvGSA_1.2.0.tar.gz |
Windows Binary | cnvGSA_1.2.0.zip (32- & 64-bit) |
MacOS 10.5 (Leopard) | cnvGSA_1.2.0.tgz |
Package Downloads Report | Download Stats |
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