Evidence map›Paper›PMID 31296220›Full record

ArticleBMC medical genomics2019

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

Sungyoung Lee, Sunmee Kim, Yongkang Kim, Bermseok Oh, Heungsun Hwang, Taesung Park

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Article in BMC medical genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sungyoung LeeCenter for Precision Medicine, Seoul National University Hospital, Seoul, Korea.
Sunmee KimDepartment of Psychology, McGill University, Montreal, Canada.
Yongkang KimDepartment of Statistics, Seoul National University, Seoul, Korea.
Bermseok OhDepartment of Biochemistry and Molecular Biology, School of Medicine, Kyung Hee University, Seoul, Korea.
Heungsun HwangDepartment of Psychology, McGill University, Montreal, Canada.
Taesung ParkDepartment of Statistics, Seoul National University, Seoul, Korea. heungsun.hwang@mcgill.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundsRecent 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.

resultsThrough 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.

conclusionIn 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/ .

Indexed as

Genetic VariationPhenotypeCluster AnalysisComputational BiologyExome SequencingClustered phenotypesGeneralized estimating equationsPathway analysisRare variants

Identifiers

PMID31296220
PMCPMC6624181

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.