GWsignif (1.2)

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Estimating Genome-Wide Significance for Whole Genome Sequencing Studies, Either Single SNP Tests or Region-Based Tests.

http://cran.r-project.org/web/packages/GWsignif

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.

Maintainer: ChangJiang Xu
Author(s): ChangJiang Xu and Celia M.T. Greenwood

License: GPL (>= 2)

Uses: Does not use any package

Released about 3 years ago.


2 previous versions

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