cnvGSA: Gene Set Analysis of (Rare) Copy Number Variants

This package is intended to facilitate gene-set association with rare CNVs in case-control studies.

Package details

AuthorDaniele Merico <[email protected]>, Robert Ziman <[email protected]>; packaged by Joseph Lugo <[email protected]>
Bioconductor views MultipleComparison
MaintainerJoseph Lugo <[email protected]>
Package repositoryView on Bioconductor
Installation Install the latest version of this package by entering the following in R:

Try the cnvGSA package in your browser

Any scripts or data that you put into this service are public.

cnvGSA documentation built on May 6, 2019, 2:41 a.m.