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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