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RareComb: Combinatorial and Statistical Analyses of Rare Events

A custom implementation of the apriori algorithm and binomial tests to identify combinations of features (genes, variants etc) significantly enriched for simultaneous mutations/events from sparse Boolean input, see Vijay Kumar Pounraja, Santhosh Girirajan (2021). Version 1.1 includes a minor adjustment to the number of combinations to be considered for multiple testing correction. This updated version is more conservative in its approach and hence more selective. <doi:10.1101/2021.10.01.462832>.

Version:1.1
Depends:R (≥ 2.10)
Imports:magrittr,arules,dplyr, methods,pwr,stringr,tidyr,reshape2,sqldf
Published:2022-02-24
DOI:10.32614/CRAN.package.RareComb
Author:Vijay Kumar PounrajaORCID iD [aut, cre]
Maintainer:Vijay Kumar Pounraja <vijaykumar.mp at gmail.com>
License:MIT + fileLICENSE
NeedsCompilation:no
Materials:README
CRAN checks:RareComb results

Documentation:

Reference manual:RareComb.html ,RareComb.pdf

Downloads:

Package source: RareComb_1.1.tar.gz
Windows binaries: r-devel:RareComb_1.1.zip, r-release:RareComb_1.1.zip, r-oldrel:RareComb_1.1.zip
macOS binaries: r-release (arm64):RareComb_1.1.tgz, r-oldrel (arm64):RareComb_1.1.tgz, r-release (x86_64):RareComb_1.1.tgz, r-oldrel (x86_64):RareComb_1.1.tgz
Old sources: RareComb archive

Linking:

Please use the canonical formhttps://CRAN.R-project.org/package=RareCombto link to this page.


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