print.BeviMed

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

<dl><dt>x</dt>
<dd><code>BeviMed</code> object.</dd>
<dt>...</dt>
<dd>Arguments passed to <code>summary.BeviMed</code></dd></dl>

Arguments

Print readable summary of BeviMed object — print.BeviMed

<dl>

<dt>x</dt>
<dd><code>BeviMed</code> object.</dd>


<dt>...</dt>
<dd>Arguments passed to <code>summary.BeviMed</code></dd>

</dl>

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

Description

Usage

Value

Arguments

See Also