prop_cov

<p>data.frame with a binary 'covered' column</p>

<p>Proportion of simulated credible sets containing the causal variant</p>

Using a computationally efficient method, the package can
be used to find the corrected coverage estimate of a credible set
of putative causal variants from Bayesian genetic fine-mapping.
The package can also be used to obtain a corrected credible set
if required; that is, the smallest set of variants required such
that the corrected coverage estimate of the resultant credible set is
within some user defined accuracy of the desired coverage.
Maller et al. (2012) <doi:10.1038/ng.2435>,
Wakefield (2009) <doi:10.1002/gepi.20359>,
Fortune and Wallace (2018) <doi:10.1093/bioinformatics/bty898>.

Anna Hutchinson

corrcoverage

prop_cov: Proportion of credible sets containing the causal variant

Description

Usage

Arguments

Value