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A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways
Gene-based, pathway, and other multivariate association methods are motivated by the possibility of GxG and GxE interactions; however, accounting for such interactions is limited by the challenges associated with adequate modeling information. Here we propose an easy-to-implement joint location-scal...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572492/ https://www.ncbi.nlm.nih.gov/pubmed/26140448 http://dx.doi.org/10.1016/j.ajhg.2015.05.015 |
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author | Soave, David Corvol, Harriet Panjwani, Naim Gong, Jiafen Li, Weili Boëlle, Pierre-Yves Durie, Peter R. Paterson, Andrew D. Rommens, Johanna M. Strug, Lisa J. Sun, Lei |
author_facet | Soave, David Corvol, Harriet Panjwani, Naim Gong, Jiafen Li, Weili Boëlle, Pierre-Yves Durie, Peter R. Paterson, Andrew D. Rommens, Johanna M. Strug, Lisa J. Sun, Lei |
author_sort | Soave, David |
collection | PubMed |
description | Gene-based, pathway, and other multivariate association methods are motivated by the possibility of GxG and GxE interactions; however, accounting for such interactions is limited by the challenges associated with adequate modeling information. Here we propose an easy-to-implement joint location-scale (JLS) association testing framework for single-variant and multivariate analysis that accounts for interactions without explicitly modeling them. We apply the JLS method to a gene-set analysis of cystic fibrosis (CF) lung disease, which is influenced by multiple environmental and genetic factors. We identify and replicate an association between the constituents of the apical plasma membrane and CF lung disease (p = 0.0099 and p = 0.0180, respectively) and highlight a role for the SLC9A3-SLC9A3R1/2-EZR complex in contributing to CF lung disease. Many association studies could benefit from re-analysis with the JLS method that leverages complex genetic architecture for SNP, gene, and pathway identification. Analytical verification, simulation, and additional proof-of-principle applications support our approach. |
format | Online Article Text |
id | pubmed-4572492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-45724922016-01-02 A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways Soave, David Corvol, Harriet Panjwani, Naim Gong, Jiafen Li, Weili Boëlle, Pierre-Yves Durie, Peter R. Paterson, Andrew D. Rommens, Johanna M. Strug, Lisa J. Sun, Lei Am J Hum Genet Article Gene-based, pathway, and other multivariate association methods are motivated by the possibility of GxG and GxE interactions; however, accounting for such interactions is limited by the challenges associated with adequate modeling information. Here we propose an easy-to-implement joint location-scale (JLS) association testing framework for single-variant and multivariate analysis that accounts for interactions without explicitly modeling them. We apply the JLS method to a gene-set analysis of cystic fibrosis (CF) lung disease, which is influenced by multiple environmental and genetic factors. We identify and replicate an association between the constituents of the apical plasma membrane and CF lung disease (p = 0.0099 and p = 0.0180, respectively) and highlight a role for the SLC9A3-SLC9A3R1/2-EZR complex in contributing to CF lung disease. Many association studies could benefit from re-analysis with the JLS method that leverages complex genetic architecture for SNP, gene, and pathway identification. Analytical verification, simulation, and additional proof-of-principle applications support our approach. Elsevier 2015-07-02 /pmc/articles/PMC4572492/ /pubmed/26140448 http://dx.doi.org/10.1016/j.ajhg.2015.05.015 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Article Soave, David Corvol, Harriet Panjwani, Naim Gong, Jiafen Li, Weili Boëlle, Pierre-Yves Durie, Peter R. Paterson, Andrew D. Rommens, Johanna M. Strug, Lisa J. Sun, Lei A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways |
title | A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways |
title_full | A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways |
title_fullStr | A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways |
title_full_unstemmed | A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways |
title_short | A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways |
title_sort | joint location-scale test improves power to detect associated snps, gene sets, and pathways |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572492/ https://www.ncbi.nlm.nih.gov/pubmed/26140448 http://dx.doi.org/10.1016/j.ajhg.2015.05.015 |
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