Package: GWsignif
Type: Package
Title: Estimating Genome-Wide Significance for Whole Genome Sequencing
        Studies, Either Single SNP Tests or Region-Based Tests
Version: 1.2.1
Description: 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. 
Authors@R: c(
  person("Changjiang", "Xu", email = "changjiang.h.xu@gmail.com", role = c("aut", "cre")),
  person("Celia M.T.", "Greenwood", role = "ctb"))
License: GPL (>= 2)
NeedsCompilation: no
Packaged: 2026-01-21 19:34:18 UTC; changjiangxu
Author: Changjiang Xu [aut, cre],
  Celia M.T. Greenwood [ctb]
Maintainer: Changjiang Xu <changjiang.h.xu@gmail.com>
Repository: CRAN
Date/Publication: 2026-01-21 19:50:07 UTC
Built: R 4.6.0; ; 2026-04-25 19:26:25 UTC; unix
