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BeviMed

Bayesian Evaluation of Variant Involvement in Mendelian Disease

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>.

Versions across snapshots

VersionRepositoryFileSize
7.0 rolling linux/jammy R-4.5 BeviMed_7.0.tar.gz 387.1 KiB
7.0 rolling linux/noble R-4.5 BeviMed_7.0.tar.gz 390.0 KiB
7.0 rolling source/ R- BeviMed_7.0.tar.gz 242.0 KiB
7.0 latest linux/jammy R-4.5 BeviMed_7.0.tar.gz 387.1 KiB
7.0 latest linux/noble R-4.5 BeviMed_7.0.tar.gz 390.0 KiB
7.0 latest source/ R- BeviMed_7.0.tar.gz 242.0 KiB
7.0 2026-04-26 source/ R- BeviMed_7.0.tar.gz 242.0 KiB
7.0 2026-04-23 source/ R- BeviMed_7.0.tar.gz 242.0 KiB
7.0 2026-04-09 windows/windows R-4.5 BeviMed_7.0.zip 712.0 KiB
5.10 2025-04-20 source/ R- BeviMed_5.10.tar.gz 230.8 KiB

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