_            _    _        _         _
      /\ \         /\ \ /\ \     /\_\      / /\
      \_\ \       /  \ \\ \ \   / / /     / /  \
      /\__ \     / /\ \ \\ \ \_/ / /     / / /\ \__
     / /_ \ \   / / /\ \ \\ \___/ /     / / /\ \___\
    / / /\ \ \ / / /  \ \_\\ \ \_/      \ \ \ \/___/
   / / /  \/_// / /   / / / \ \ \        \ \ \
  / / /      / / /   / / /   \ \ \   _    \ \ \
 / / /      / / /___/ / /     \ \ \ /_/\__/ / /
/_/ /      / / /____\/ /       \ \_\\ \/___/ /
\_\/       \/_________/         \/_/ \_____\/
r-cnvgsa 1.52.0
Propagated dependencies: r-splitstackshape@1.4.8 r-genomicranges@1.60.0 r-foreach@1.5.2 r-doparallel@1.0.17 r-brglm@0.7.2
Channel: guix-bioc
Location: guix-bioc/packages/c.scm (guix-bioc packages c)
Home page: https://bioconductor.org/packages/cnvGSA
Licenses: LGPL 2.0+
Synopsis: Gene Set Analysis of (Rare) Copy Number Variants
Description:

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

Total results: 2