Cargando…

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

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Sungyoung, Kim, Sunmee, Kim, Yongkang, Oh, Bermseok, Hwang, Heungsun, Park, Taesung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624181/
https://www.ncbi.nlm.nih.gov/pubmed/31296220
http://dx.doi.org/10.1186/s12920-019-0517-4
_version_ 1783434216880472064
author Lee, Sungyoung
Kim, Sunmee
Kim, Yongkang
Oh, Bermseok
Hwang, Heungsun
Park, Taesung
author_facet Lee, Sungyoung
Kim, Sunmee
Kim, Yongkang
Oh, Bermseok
Hwang, Heungsun
Park, Taesung
author_sort Lee, Sungyoung
collection PubMed
description 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/.
format Online
Article
Text
id pubmed-6624181
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-66241812019-07-23 Pathway analysis of rare variants for the clustered phenotypes by using hierarchical structured components analysis Lee, Sungyoung Kim, Sunmee Kim, Yongkang Oh, Bermseok Hwang, Heungsun Park, Taesung BMC Med Genomics Research 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/. BioMed Central 2019-07-11 /pmc/articles/PMC6624181/ /pubmed/31296220 http://dx.doi.org/10.1186/s12920-019-0517-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lee, Sungyoung
Kim, Sunmee
Kim, Yongkang
Oh, Bermseok
Hwang, Heungsun
Park, Taesung
Pathway analysis of rare variants for the clustered phenotypes by using hierarchical structured components analysis
title Pathway analysis of rare variants for the clustered phenotypes by using hierarchical structured components analysis
title_full Pathway analysis of rare variants for the clustered phenotypes by using hierarchical structured components analysis
title_fullStr Pathway analysis of rare variants for the clustered phenotypes by using hierarchical structured components analysis
title_full_unstemmed Pathway analysis of rare variants for the clustered phenotypes by using hierarchical structured components analysis
title_short Pathway analysis of rare variants for the clustered phenotypes by using hierarchical structured components analysis
title_sort pathway analysis of rare variants for the clustered phenotypes by using hierarchical structured components analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624181/
https://www.ncbi.nlm.nih.gov/pubmed/31296220
http://dx.doi.org/10.1186/s12920-019-0517-4
work_keys_str_mv AT leesungyoung pathwayanalysisofrarevariantsfortheclusteredphenotypesbyusinghierarchicalstructuredcomponentsanalysis
AT kimsunmee pathwayanalysisofrarevariantsfortheclusteredphenotypesbyusinghierarchicalstructuredcomponentsanalysis
AT kimyongkang pathwayanalysisofrarevariantsfortheclusteredphenotypesbyusinghierarchicalstructuredcomponentsanalysis
AT ohbermseok pathwayanalysisofrarevariantsfortheclusteredphenotypesbyusinghierarchicalstructuredcomponentsanalysis
AT hwangheungsun pathwayanalysisofrarevariantsfortheclusteredphenotypesbyusinghierarchicalstructuredcomponentsanalysis
AT parktaesung pathwayanalysisofrarevariantsfortheclusteredphenotypesbyusinghierarchicalstructuredcomponentsanalysis