GWsignif
Estimating Genome-Wide Significance for Whole Genome Sequencing Studies, Either Single SNP Tests or Region-Based Tests
The correlations and linkage disequilibrium between tests can vary as a function of minor allele frequency thresholds used to filter variants, and also varies with different choices of test statistic for region-based tests. Appropriate genome-wide significance thresholds can be estimated empirically through permutation on only a small proportion of the whole genome.
Versions across snapshots
| Version | Repository | File | Size |
|---|---|---|---|
1.2.1 |
rolling source/ R- | GWsignif_1.2.1.tar.gz |
4.7 KiB |
1.2.1 |
rolling linux/jammy R-4.5 | GWsignif_1.2.1.tar.gz |
20.4 KiB |
1.2.1 |
rolling linux/noble R-4.5 | GWsignif_1.2.1.tar.gz |
20.3 KiB |
1.2.1 |
latest source/ R- | GWsignif_1.2.1.tar.gz |
4.7 KiB |
1.2.1 |
latest linux/jammy R-4.5 | GWsignif_1.2.1.tar.gz |
20.4 KiB |
1.2.1 |
latest linux/noble R-4.5 | GWsignif_1.2.1.tar.gz |
20.3 KiB |
1.2.1 |
2026-04-23 source/ R- | GWsignif_1.2.1.tar.gz |
4.7 KiB |
1.2.1 |
2026-04-09 windows/windows R-4.5 | GWsignif_1.2.1.zip |
23.0 KiB |
1.2 |
2025-04-20 source/ R- | GWsignif_1.2.tar.gz |
4.6 KiB |