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>
License: GPL-2 | GPL-3 [expanded from: GPL (≥ 2)]
NeedsCompilation: yes
CRAN checks: BeviMed results


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


Please use the canonical form to link to this page.