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.


Reference manual

It appears you don't have a PDF plugin for this browser. You can click here to download the reference manual.

install.packages("GWsignif")

1.2.1 by Changjiang Xu, 8 months ago


Browse source code at https://github.com/cran/GWsignif


Authors: Changjiang Xu [aut, cre] , Celia M.T. Greenwood [ctb]


Documentation:   PDF Manual  


GPL (>= 2) license



See at CRAN