Functions in this package will import filtered variant call format (VCF) files of SNPs data and generate data sets to detect copy number variants, visualize them and do downstream analyses with copy number variants(e.g. Environmental association analyses).
Version: 1.3.0 Depends: R (≥ 3.6.0) Imports: data.table, graphics, colorspace, R.utils, qgraph, stringr Suggests: rmarkdown, knitr, testthat (≥ 3.0.0), covr Published: 2024-09-20 DOI: 10.32614/CRAN.package.rCNV Author: Piyal Karunarathne [aut, cre], Qiujie Zhou [aut], Klaus Schliep [aut], Pascal Milesi [aut] Maintainer: Piyal Karunarathne <piyalkarumail at yahoo.com> BugReports: https://github.com/piyalkarum/rCNV/issues License: AGPL (≥ 3) URL: https://piyalkarum.github.io/rCNV/, https://cran.r-project.org/package=rCNV NeedsCompilation: no Language: en-US Citation: rCNV citation info Materials: README NEWS CRAN checks: rCNV results Documentation: Downloads: Linking:Please use the canonical form https://CRAN.R-project.org/package=rCNV to link to this page.
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