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Showing content from http://cran.rstudio.com/web/packages/Rcpp/../SparseICA/../Rcpp/../Rfast/../NGBVS/index.html below:

CRAN: Package NGBVS

NGBVS: Bayesian Variable Selection for SNP Data using Normal-Gamma

Posterior distribution of case-control fine-mapping. Specifically, Bayesian variable selection for single-nucleotide polymorphism (SNP) data using the normal-gamma prior. Alenazi A.A., Cox A., Juarez M,. Lin W-Y. and Walters, K. (2019) Bayesian variable selection using partially observed categorical prior information in fine-mapping association studies, Genetic Epidemiology. <doi:10.1002/gepi.22213>.

Version: 0.3.0 Depends: R (≥ 3.6.0) Imports: stats, Rfast Published: 2022-09-16 DOI: 10.32614/CRAN.package.NGBVS Author: Abdulaziz Alenazi [aut, cre] Maintainer: Abdulaziz Alenazi <a.alenazi at nbu.edu.sa> License: GPL-2 | GPL-3 [expanded from: GPL (≥ 2)] NeedsCompilation: no CRAN checks: NGBVS results Documentation: Downloads: Linking:

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