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A Fully Automated Parallel-Processing R Package for High-Dimensional Multiple-Phenotype Analysis Considering Population Structureopen access

Authors
Lee, Gi JuPark, Sung MinJung, JunghyunJoo, Jong Wha J.
Issue Date
Sep-2020
Publisher
KOREAN INST INTELLIGENT SYSTEMS
Keywords
GWAS; Multiple-phenotype analysis; Population structure; R package
Citation
INTERNATIONAL JOURNAL OF FUZZY LOGIC AND INTELLIGENT SYSTEMS, v.20, no.3, pp 219 - 226
Pages
8
Indexed
SCOPUS
ESCI
KCI
Journal Title
INTERNATIONAL JOURNAL OF FUZZY LOGIC AND INTELLIGENT SYSTEMS
Volume
20
Number
3
Start Page
219
End Page
226
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/17905
DOI
10.5391/IJFIS.2020.20.3.219
ISSN
1598-2645
2093-744X
Abstract
A typical genome-wide association study is conducted through a single-phenotype analysis of the correlation between each phenotype and genotype one at a time. Alternatively, a multiple-phenotype analysis of the correlation between multiple phenotypes and a genotype often has many advantages over single-phenotype analysis. For example, statistical power in the association test may be increased in a multiple-phenotype analysis and thus may detect small effects that cannot be identified in a single-phenotype analysis. Of the several multiple-phenotype analytical methods that have been proposed, generalized analysis of molecular variance for mixed-model analysis (GAMMA) is used to analyze many phenotypes simultaneously while considering the population structure. This method shows higher accuracy than the other methods. However, GAMMA has not been widely used because no automated and user-friendly software is available; this is also the case with most other multiple-phenotype analysis methods. In addition, the lack of a parallel-processing option, which is essential in a genome-wide-association-studies analysis, is also prevalent in GAMMA. In this study, we propose an easy-to-use R package for GAMMA called GAMMA Renew (GAMMAR) that performs multiple-phenotype analysis using parallel processing. We evaluate GAMMAR using a recently published yeast dataset to locate trans-regulatory hotspots.
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