Bioconductor version: Release (2.12)
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 | 1.4.0 | 
| 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_1.4.0.tar.gz | 
| Windows Binary | cnvGSA_1.4.0.zip (32- & 64-bit) | 
| Mac OS X 10.6 (Snow Leopard) | cnvGSA_1.4.0.tgz | 
| Package Downloads Report | Download Stats | 
 
  
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