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Pathway analysis for genetic association studies: to do, or not to do? That is the question
In Genetic Analysis Workshop 18 data, we used a 3-stage approach to explore the benefits of pathway analysis in improving a model to predict 2 diastolic blood pressure phenotypes as a function of genetic variation. At stage 1, gene-based tests of association in family data of approximately 800 indiv...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4144468/ https://www.ncbi.nlm.nih.gov/pubmed/25519357 http://dx.doi.org/10.1186/1753-6561-8-S1-S103 |
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author | Dufresne, Line Oualkacha, Karim Forgetta, Vincenzo Greenwood, Celia MT |
author_facet | Dufresne, Line Oualkacha, Karim Forgetta, Vincenzo Greenwood, Celia MT |
author_sort | Dufresne, Line |
collection | PubMed |
description | In Genetic Analysis Workshop 18 data, we used a 3-stage approach to explore the benefits of pathway analysis in improving a model to predict 2 diastolic blood pressure phenotypes as a function of genetic variation. At stage 1, gene-based tests of association in family data of approximately 800 individuals found over 600 genes associated at p<0.05 for each phenotype. At stage 2, networks and enriched pathways were estimated with Cytoscape for genes from stage 1, separately for the 2 phenotypes, then examining network overlap. This overlap identified 4 enriched pathways, and 3 of these pathways appear to interact, and are likely candidates for playing a role in hypertension. At stage 3, using 157 maximally unrelated individuals, partial least squares regression was used to find associations between diastolic blood pressure and single-nucleotide polymorphisms in genes highlighted by the pathway analyses. However, we saw no improvement in the adjusted cross-validated R(2). Although our pathway-motivated regressions did not improve prediction of diastolic blood pressure, merging gene networks did identify several plausible pathways for hypertension. |
format | Online Article Text |
id | pubmed-4144468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41444682014-09-02 Pathway analysis for genetic association studies: to do, or not to do? That is the question Dufresne, Line Oualkacha, Karim Forgetta, Vincenzo Greenwood, Celia MT BMC Proc Proceedings In Genetic Analysis Workshop 18 data, we used a 3-stage approach to explore the benefits of pathway analysis in improving a model to predict 2 diastolic blood pressure phenotypes as a function of genetic variation. At stage 1, gene-based tests of association in family data of approximately 800 individuals found over 600 genes associated at p<0.05 for each phenotype. At stage 2, networks and enriched pathways were estimated with Cytoscape for genes from stage 1, separately for the 2 phenotypes, then examining network overlap. This overlap identified 4 enriched pathways, and 3 of these pathways appear to interact, and are likely candidates for playing a role in hypertension. At stage 3, using 157 maximally unrelated individuals, partial least squares regression was used to find associations between diastolic blood pressure and single-nucleotide polymorphisms in genes highlighted by the pathway analyses. However, we saw no improvement in the adjusted cross-validated R(2). Although our pathway-motivated regressions did not improve prediction of diastolic blood pressure, merging gene networks did identify several plausible pathways for hypertension. BioMed Central 2014-06-17 /pmc/articles/PMC4144468/ /pubmed/25519357 http://dx.doi.org/10.1186/1753-6561-8-S1-S103 Text en Copyright © 2014 Dufresne et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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 | Proceedings Dufresne, Line Oualkacha, Karim Forgetta, Vincenzo Greenwood, Celia MT Pathway analysis for genetic association studies: to do, or not to do? That is the question |
title | Pathway analysis for genetic association studies: to do, or not to do? That is the
question |
title_full | Pathway analysis for genetic association studies: to do, or not to do? That is the
question |
title_fullStr | Pathway analysis for genetic association studies: to do, or not to do? That is the
question |
title_full_unstemmed | Pathway analysis for genetic association studies: to do, or not to do? That is the
question |
title_short | Pathway analysis for genetic association studies: to do, or not to do? That is the
question |
title_sort | pathway analysis for genetic association studies: to do, or not to do? that is the
question |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4144468/ https://www.ncbi.nlm.nih.gov/pubmed/25519357 http://dx.doi.org/10.1186/1753-6561-8-S1-S103 |
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