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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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 |
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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 |
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