Package: BeviMed
Type: Package
Title: Bayesian Evaluation of Variant Involvement in Mendelian Disease
Version: 7.0
Encoding: UTF-8
Date: 2025-08-20
Authors@R: person("Daniel", "Greene", email = "dg333@cam.ac.uk",role = c("aut", "cre"))
Description: 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>.
License: GPL (>= 2)
Imports: Rcpp (>= 0.12.3), Matrix, methods
LinkingTo: Rcpp
Depends: R (>= 3.0.0)
Suggests: rmarkdown, knitr
RoxygenNote: 7.3.2
VignetteBuilder: knitr
NeedsCompilation: yes
Packaged: 2026-06-18 10:54:27 UTC; root
Author: Daniel Greene [aut, cre]
Maintainer: Daniel Greene <dg333@cam.ac.uk>
Repository: https://daniel-jg.r-universe.dev
Date/Publication: 2025-08-22 07:30:01 UTC
RemoteUrl: https://github.com/cran/BeviMed
RemoteRef: HEAD
RemoteSha: f2caaa0b6696ffa6ac16f0731326adbb7015d10f