corrcoverage
1.2.1Correcting the Coverage of Credible Sets from Bayesian Genetic Fine Mapping
Overview
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.
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- 82%
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- Return-value docs
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People & History
4 releases. Pick two to compare their code metrics. R releases are shown for context.
- RR 4.6.0 released · 2026-04-24
- archivedRemoved from CRAN2025-09-17email to the maintainer is undeliverable
- RR 4.5.0 released · 2025-04-11
- RR 4.4.0 released · 2024-04-24
- RR 4.3.0 released · 2023-04-21
- RR 4.2.0 released · 2022-04-22
- RR 4.1.0 released · 2021-05-18
- RR 4.0.0 released · 2020-04-24
- 1.2.12019-12-06 · diff ↗
- 1.2.02019-12-05 · diff ↗
- 1.1.02019-09-05 · diff ↗
- 1.0.02019-08-28
- RR 3.6.0 released · 2019-04-26
Package metadata
- Total releases
- 4
- License
- MIT + file LICENSE OSI
- Minimum R
- ≥ 3.5.0
- Download size
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