print.BeviMed

Arguments passed to <code><a rd-options="" href="/link/summary.BeviMed?package=BeviMed&version=5.3" data-mini-rdoc="BeviMed::summary.BeviMed">summary.BeviMed</a></code>

Print summary statistics of BeviMed inference, including probability of association, probability of dominant inheritance given association and probability of pathogenicity of each variant under dominant and recessive inheritance.

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>.

Daniel Greene

BeviMed

Bayesian Evaluation of Variant Involvement in Mendelian Disease

print.BeviMed function

Arguments passed to <code><a rd-options='' href='summary.BeviMed'>summary.BeviMed</a></code>

print.BeviMed: Print readable summary of `BeviMed` object

Description

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See Also