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# CITATION file created with {cffr} R package
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cff-version: 1.2.0
message: 'To cite package "GWsignif" in publications use:'
type: software
license: GPL-2.0-or-later
title: 'GWsignif: Estimating Genome-Wide Significance for Whole Genome Sequencing
  Studies, Either Single SNP Tests or Region-Based Tests'
version: '1.2'
doi: 10.32614/CRAN.package.GWsignif
abstract: 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:
- family-names: Xu
  given-names: ChangJiang
  email: changjiang.h.xu@gmail.com
- family-names: Greenwood
  given-names: Celia M.T.
repository: https://changjiangxu.r-universe.dev
commit: 5d37dbc85fc990cec970aa0d9a7ac320fe882d95
date-released: '2016-09-10'
contact:
- family-names: Xu
  given-names: ChangJiang
  email: changjiang.h.xu@gmail.com