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BeviMed  

Bayesian Evaluation of Variant Involvement in Mendelian Disease
View on CRAN: Click here


Download and install BeviMed package within the R console
Install from CRAN:
install.packages("BeviMed")

Install from Github:
library("remotes")
install_github("cran/BeviMed")

Install by package version:
library("remotes")
install_version("BeviMed", "7.0")



Attach the package and use:
library("BeviMed")
Maintained by
Daniel Greene
[Scholar Profile | Author Map]
All associated links for this package
First Published: 2016-05-03
Latest Update: 2025-04-29
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 .
How to cite:
Daniel Greene (2016). BeviMed: Bayesian Evaluation of Variant Involvement in Mendelian Disease. R package version 7.0, https://cran.r-project.org/web/packages/BeviMed. Accessed 26 Aug. 2026.
Previous versions and publish date:
1.2 (2016-05-03 08:20), 2.2 (2016-07-05 23:43), 3.0 (2017-02-16 17:27), 4.0 (2017-03-01 08:36), 5.0 (2017-04-22 18:21), 5.1 (2017-07-03 12:25), 5.3 (2017-08-21 18:00), 5.7 (2020-03-28 14:20), 5.8 (2021-02-01 00:20), 5.10 (2024-05-29 21:50), 6.0 (2025-04-29 19:10), (2026-07-09 07:58)
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Complete documentation for BeviMed
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