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>.

Package details

AuthorDaniel Greene, Sylvia Richardson and Ernest Turro
MaintainerDaniel Greene <dg333@cam.ac.uk>
LicenseGPL (>= 2)
Version5.7
Package repositoryView on CRAN
Installation Install the latest version of this package by entering the following in R:
install.packages("BeviMed")

Try the BeviMed package in your browser

Any scripts or data that you put into this service are public.

BeviMed documentation built on March 31, 2020, 5:17 p.m.