Bayesian Evaluation of Variant Involvement in Mendelian Disease R package BeviMed version 7.0 A fast integrative genetic association test for rare diseases based on a model for disease status given allele counts at rare variant sites. Probability of association, mode of inheritance and probability of pathogenicity for individual variants are all inferred in a Bayesian framework - 'A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases', Greene et al 2017 <doi:10.1016/j.ajhg.2017.05.015>. Software Depends: R (>= 3.0.0) Imports: Rcpp (>= 0.12.3), Matrix, methods LinkingTo: Rcpp Suggests: rmarkdown, knitr Daniel Greene <dg333@cam.ac.uk> Comprehensive R Archive Network (CRAN) Daniel Greene [aut, cre] GPL (>= 2) 2025-08-22 application/tgz https://CRAN.R-project.org/package=BeviMed doi:10.32614/CRAN.package.BeviMed