# -------------------------------------------- # CITATION file created with {cffr} R package # See also: https://docs.ropensci.org/cffr/ # -------------------------------------------- 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