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Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations
We introduce pleiotropic association test (PAT) for joint analysis of multiple traits using genome-wide association study (GWAS) summary statistics. The method utilizes the decomposition of phenotypic covariation into genetic and environmental components to create a likelihood ratio test statistic f...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671458/ https://www.ncbi.nlm.nih.gov/pubmed/36342933 http://dx.doi.org/10.1371/journal.pgen.1010447 |
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author | Taraszka, Kodi Zaitlen, Noah Eskin, Eleazar |
author_facet | Taraszka, Kodi Zaitlen, Noah Eskin, Eleazar |
author_sort | Taraszka, Kodi |
collection | PubMed |
description | We introduce pleiotropic association test (PAT) for joint analysis of multiple traits using genome-wide association study (GWAS) summary statistics. The method utilizes the decomposition of phenotypic covariation into genetic and environmental components to create a likelihood ratio test statistic for each genetic variant. Though PAT does not directly interpret which trait(s) drive the association, a per trait interpretation of the omnibus p-value is provided through an extension to the meta-analysis framework, m-values. In simulations, we show PAT controls the false positive rate, increases statistical power, and is robust to model misspecifications of genetic effect. Additionally, simulations comparing PAT to three multi-trait methods, HIPO, MTAG, and ASSET, show PAT identified 15.3% more omnibus associations over the next best method. When these associations were interpreted on a per trait level using m-values, PAT had 37.5% more true per trait interpretations with a 0.92% false positive assignment rate. When analyzing four traits from the UK Biobank, PAT discovered 22,095 novel variants. Through the m-values interpretation framework, the number of per trait associations for two traits were almost tripled and were nearly doubled for another trait relative to the original single trait GWAS. |
format | Online Article Text |
id | pubmed-9671458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-96714582022-11-18 Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations Taraszka, Kodi Zaitlen, Noah Eskin, Eleazar PLoS Genet Research Article We introduce pleiotropic association test (PAT) for joint analysis of multiple traits using genome-wide association study (GWAS) summary statistics. The method utilizes the decomposition of phenotypic covariation into genetic and environmental components to create a likelihood ratio test statistic for each genetic variant. Though PAT does not directly interpret which trait(s) drive the association, a per trait interpretation of the omnibus p-value is provided through an extension to the meta-analysis framework, m-values. In simulations, we show PAT controls the false positive rate, increases statistical power, and is robust to model misspecifications of genetic effect. Additionally, simulations comparing PAT to three multi-trait methods, HIPO, MTAG, and ASSET, show PAT identified 15.3% more omnibus associations over the next best method. When these associations were interpreted on a per trait level using m-values, PAT had 37.5% more true per trait interpretations with a 0.92% false positive assignment rate. When analyzing four traits from the UK Biobank, PAT discovered 22,095 novel variants. Through the m-values interpretation framework, the number of per trait associations for two traits were almost tripled and were nearly doubled for another trait relative to the original single trait GWAS. Public Library of Science 2022-11-07 /pmc/articles/PMC9671458/ /pubmed/36342933 http://dx.doi.org/10.1371/journal.pgen.1010447 Text en © 2022 Taraszka et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Taraszka, Kodi Zaitlen, Noah Eskin, Eleazar Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations |
title | Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations |
title_full | Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations |
title_fullStr | Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations |
title_full_unstemmed | Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations |
title_short | Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations |
title_sort | leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671458/ https://www.ncbi.nlm.nih.gov/pubmed/36342933 http://dx.doi.org/10.1371/journal.pgen.1010447 |
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