BeviMed: Bayesian Evaluation of Variant Involvement in Mendelian Disease (original) (raw)
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>.
Version: | 5.10 |
---|---|
Depends: | R (≥ 3.0.0) |
Imports: | Rcpp (≥ 0.12.3), Matrix, methods |
LinkingTo: | Rcpp |
Suggests: | rmarkdown, knitr |
Published: | 2024-05-29 |
DOI: | 10.32614/CRAN.package.BeviMed |
Author: | Daniel Greene, Sylvia Richardson and Ernest Turro |
Maintainer: | Daniel Greene |
License: | GPL-2 | GPL-3 [expanded from: GPL (≥ 2)] |
NeedsCompilation: | yes |
Citation: | BeviMed citation info |
Materials: | NEWS |
CRAN checks: | BeviMed results |
Documentation:
Downloads:
Linking:
Please use the canonical formhttps://CRAN.R-project.org/package=BeviMedto link to this page.