cnvGSA
Gene Set Analysis of (Rare) Copy Number Variants
Bioconductor version: 3.23 · Package version: 1.56.0
This package is intended to facilitate gene-set association with rare CNVs in case-control studies.
Installation
if (!require("BiocManager", quietly = TRUE))
install.packages("BiocManager")
BiocManager::install("cnvGSA")Details
| Maintainer | Joseph Lugo <joseph.r.lugo@gmail.com> |
| Author | Daniele Merico <daniele.merico@gmail.com>, Robert Ziman <rziman@gmail.com>; packaged by Joseph Lugo <joseph.r.lugo@gmail.com> |
| License | LGPL |
| Downloads rank | 484 |
| Source branch | RELEASE_3_23 |
| biocViews | MultipleComparison, Software |
Documentation
Download
Follow the installation instructions to use this package in your R session.
| Source package | cnvGSA_1.56.0.tar.gz |
| Windows binary (x86_64) | cnvGSA_1.56.0.zip |
| macOS binary (arm64) | cnvGSA_1.56.0.tgz |
| macOS binary (x86_64) | cnvGSA_1.56.0.tgz |
Dependencies
Depends: brglm, doParallel, foreach, GenomicRanges, methods, splitstackshape
Suggests: cnvGSAdata, org.Hs.eg.db
Reverse dependencies
Depends On Me (1): cnvGSAdata