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>.
Versions across snapshots
| Version | Repository | File | Size |
|---|---|---|---|
0.3.0 |
rolling linux/jammy R-4.5 | NGBVS_0.3.0.tar.gz |
63.9 KiB |
0.3.0 |
rolling linux/noble R-4.5 | NGBVS_0.3.0.tar.gz |
63.8 KiB |
0.3.0 |
rolling source/ R- | NGBVS_0.3.0.tar.gz |
7.5 KiB |
0.3.0 |
latest linux/jammy R-4.5 | NGBVS_0.3.0.tar.gz |
63.9 KiB |
0.3.0 |
latest linux/noble R-4.5 | NGBVS_0.3.0.tar.gz |
63.8 KiB |
0.3.0 |
latest source/ R- | NGBVS_0.3.0.tar.gz |
7.5 KiB |
0.3.0 |
2026-04-26 source/ R- | NGBVS_0.3.0.tar.gz |
7.5 KiB |
0.3.0 |
2026-04-23 source/ R- | NGBVS_0.3.0.tar.gz |
7.5 KiB |
0.3.0 |
2026-04-09 windows/windows R-4.5 | NGBVS_0.3.0.zip |
66.4 KiB |
0.3.0 |
2025-04-20 source/ R- | NGBVS_0.3.0.tar.gz |
7.5 KiB |