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Pathway analysis of rare variants for the clustered phenotypes by using hierarchical structured components analysis.

Authors :
Lee, Sungyoung
Kim, Sunmee
Kim, Yongkang
Oh, Bermseok
Hwang, Heungsun
Park, Taesung
Source :
BMC Medical Genomics. 7/11/2019 Supplement 5, Vol. 12 Issue 5, pN.PAG-N.PAG. 1p.
Publication Year :
2019

Abstract

Backgrounds: Recent large-scale genetic studies often involve clustered phenotypes such as repeated measurements. Compared to a series of univariate analyses of single phenotypes, an analysis of clustered phenotypes can be useful for substantially increasing statistical power to detect more genetic associations. Moreover, for the analysis of rare variants, incorporation of biological information can boost weak effects of the rare variants. Results: Through simulation studies, we showed that the proposed method outperforms other method currently available for pathway-level analysis of clustered phenotypes. Moreover, a real data analysis using a large-scale whole exome sequencing dataset of 995 samples with metabolic syndrome-related phenotypes successfully identified the glyoxylate and dicarboxylate metabolism pathway that could not be identified by the univariate analyses of single phenotypes and other existing method. Conclusion: In this paper, we introduced a novel pathway-level association test by combining hierarchical structured components analysis and penalized generalized estimating equations. The proposed method analyzes all pathways in a single unified model while considering their correlations. C/C++ implementation of PHARAOH-GEE is publicly available at http://statgen.snu.ac.kr/software/pharaoh-gee/. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17558794
Volume :
12
Issue :
5
Database :
Academic Search Index
Journal :
BMC Medical Genomics
Publication Type :
Academic Journal
Accession number :
137441206
Full Text :
https://doi.org/10.1186/s12920-019-0517-4