BeviMed: Bayesian Evaluation of Variant Involvement in Mendelian Disorders

Bayesian inference procedures for evaluating evidence of involvement of variants in Mendelian disorders based on intuitive models of dominant and recessive inheritance.

Version: 2.2
Depends: R (≥ 3.0.0)
Imports: Rcpp (≥ 0.12.3)
LinkingTo: Rcpp
Suggests: knitr
Published: 2016-07-05
Author: Daniel Greene
Maintainer: Daniel Greene <dg333 at cam.ac.uk>
License: GPL-2 | GPL-3 [expanded from: GPL (≥ 2)]
NeedsCompilation: yes
CRAN checks: BeviMed results

Downloads:

Reference manual: BeviMed.pdf
Vignettes: BeviMed Introduction
Package source: BeviMed_2.2.tar.gz
Windows binaries: r-devel: BeviMed_2.2.zip, r-release: BeviMed_2.2.zip, r-oldrel: BeviMed_2.2.zip
OS X Mavericks binaries: r-release: BeviMed_2.2.tgz, r-oldrel: BeviMed_2.2.tgz
Old sources: BeviMed archive

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