explaining_variants

Use <code>bevimed_m</code> to perform inference under model gamma = 1 and return only the expected number of pathogenic variants in cases.

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

explaining_variants function

<dl><dt>...</dt>
<dd>Arguments to pass to <code>bevimed_m</code>.</dd></dl>

Arguments

Calculate expected number of pathogenic variants in cases — explaining_variants

<dl>

<dt>...</dt>
<dd>Arguments to pass to <code>bevimed_m</code>.</dd>

</dl>

explaining_variants: Calculate expected number of pathogenic variants in cases

Description

Usage

Value

Arguments

See Also