GWsignif (1.2)

0 users

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.

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



  (0 votes)


  (0 votes)

Log in to vote.


No one has written a review of GWsignif yet. Want to be the first? Write one now.

Related packages:(20 best matches, based on common tags.)

Search for GWsignif on google, google scholar, r-help, r-devel.

Visit GWsignif on R Graphical Manual.