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GWsignif
View on CRAN: Click
here
Download and install GWsignif package within the R console
Install from CRAN:
install.packages("GWsignif")
Install from Github:
library("remotes")
install_github("cran/GWsignif") Install by package version:
library("remotes")
install_version("GWsignif", "1.2.1") Attach the package and use:
library("GWsignif")
Maintained by
ChangJiang Xu
[Scholar Profile | Author Map]
[Scholar Profile | Author Map]
All associated links for this package
First Published: 2014-01-15
Latest Update: 2016-09-12
Description:
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.
How to cite:
ChangJiang Xu (2014). GWsignif: Estimating Genome-Wide Significance for Whole Genome Sequencing Studies, Either Single SNP Tests or Region-Based Tests. R package version 1.2.1, https://cran.r-project.org/web/packages/GWsignif. Accessed 01 Sep. 2026.
Previous versions and publish date:
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Complete documentation for GWsignif
Functions, R codes and Examples using
the GWsignif R package
Some associated functions: GWsignif-package . GWsignif .
Some associated R codes: GWsignif.R . Full GWsignif package functions and examples
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