BeviMed: Bayesian Evaluation of Variant Involvement in Mendelian Disease
Version 5.3

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 .

Package details

AuthorDaniel Greene, Sylvia Richardson and Ernest Turro
Date of publication2017-08-21 16:00:20 UTC
MaintainerDaniel Greene <dg333@cam.ac.uk>
LicenseGPL (>= 2)
Version5.3
Package repositoryView on CRAN
Installation Install the latest version of this package by entering the following in R:
install.packages("BeviMed")

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BeviMed documentation built on Aug. 21, 2017, 5:05 p.m.