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corrcoverage  

Correcting the Coverage of Credible Sets from Bayesian Genetic Fine Mapping
View on CRAN: Click here


Download and install corrcoverage package within the R console
Install from CRAN:
install.packages("corrcoverage")

Install from Github:
library("remotes")
install_github("cran/corrcoverage")

Install by package version:
library("remotes")
install_version("corrcoverage", "1.2.1")



Attach the package and use:
library("corrcoverage")
Maintained by
Anna Hutchinson
[Scholar Profile | Author Map]
All associated links for this package
First Published: 2019-08-28
Latest Update: 2019-12-06
Description:
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) , Wakefield (2009) , Fortune and Wallace (2018) .
How to cite:
Anna Hutchinson (2019). corrcoverage: Correcting the Coverage of Credible Sets from Bayesian Genetic Fine Mapping. R package version 1.2.1, https://cran.r-project.org/web/packages/corrcoverage. Accessed 22 Dec. 2024.
Previous versions and publish date:
1.0.0 (2019-08-28 11:10), 1.1.0 (2019-09-05 11:50), 1.2.0 (2019-12-05 11:50)
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Complete documentation for corrcoverage
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