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: | 7.0 |
| Depends: | R (≥ 3.0.0) |
| Imports: | Rcpp (≥ 0.12.3),Matrix, methods |
| LinkingTo: | Rcpp |
| Suggests: | rmarkdown,knitr |
| Published: | 2025-08-22 |
| DOI: | 10.32614/CRAN.package.BeviMed |
| Author: | Daniel Greene [aut, cre] |
| Maintainer: | Daniel Greene <dg333 at cam.ac.uk> |
| License: | GPL-2 |GPL-3 [expanded from: GPL (≥ 2)] |
| NeedsCompilation: | yes |
| Citation: | BeviMed citation info |
| Materials: | NEWS |
| CRAN checks: | BeviMed results |
| Reference manual: | BeviMed.html ,BeviMed.pdf |
| Vignettes: | BeviMed Introduction (source,R code) BeviMed with VCFs (source,R code) BeviMed Guide (source,R code) |
| Package source: | BeviMed_7.0.tar.gz |
| Windows binaries: | r-devel:BeviMed_7.0.zip, r-release:BeviMed_7.0.zip, r-oldrel:BeviMed_7.0.zip |
| macOS binaries: | r-release (arm64):BeviMed_7.0.tgz, r-oldrel (arm64):BeviMed_7.0.tgz, r-release (x86_64):BeviMed_7.0.tgz, r-oldrel (x86_64):BeviMed_7.0.tgz |
| Old sources: | BeviMed archive |
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