mrMLM: Multi-Locus Random-SNP-Effect Mixed Linear Model Tools for Genome-Wide Association Study
Version 3.0

Conduct multi-locus genome-wide association study under the framework of random-SNP-effect mixed linear model (mrMLM). First, each marker on the genome is scanned. Bonferroni correction is replaced by a less stringent selection criterion for significant test. Then, all the markers that are potentially associated with the trait are included in a multi-locus model, their effects are estimated by empirical Bayes and true QTN are identified by likelihood ratio test.

Getting started

Package details

AuthorZhang Ya-Wen, Li Pei, Ren Wen-Long, Ni Yuan-Li, and Zhang Yuan-Ming
Date of publication2018-03-12 04:09:16 UTC
MaintainerYuanming Zhang<[email protected]>
LicenseGPL (>= 2)
Package repositoryView on CRAN
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mrMLM documentation built on March 18, 2018, 1:16 p.m.