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Integrated analyses of gene expression and genetic association studies in a founder population
Genome-wide association studies (GWASs) have become a standard tool for dissecting genetic contributions to disease risk. However, these studies typically require extraordinarily large sample sizes to be adequately powered. Strategies that incorporate functional information alongside genetic associa...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062579/ https://www.ncbi.nlm.nih.gov/pubmed/26931462 http://dx.doi.org/10.1093/hmg/ddw061 |
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author | Cusanovich, Darren A. Caliskan, Minal Billstrand, Christine Michelini, Katelyn Chavarria, Claudia De Leon, Sherryl Mitrano, Amy Lewellyn, Noah Elias, Jack A. Chupp, Geoffrey L. Lang, Roberto M. Shah, Sanjiv J. Decara, Jeanne M. Gilad, Yoav Ober, Carole |
author_facet | Cusanovich, Darren A. Caliskan, Minal Billstrand, Christine Michelini, Katelyn Chavarria, Claudia De Leon, Sherryl Mitrano, Amy Lewellyn, Noah Elias, Jack A. Chupp, Geoffrey L. Lang, Roberto M. Shah, Sanjiv J. Decara, Jeanne M. Gilad, Yoav Ober, Carole |
author_sort | Cusanovich, Darren A. |
collection | PubMed |
description | Genome-wide association studies (GWASs) have become a standard tool for dissecting genetic contributions to disease risk. However, these studies typically require extraordinarily large sample sizes to be adequately powered. Strategies that incorporate functional information alongside genetic associations have proved successful in increasing GWAS power. Following this paradigm, we present the results of 20 different genetic association studies for quantitative traits related to complex diseases, conducted in the Hutterites of South Dakota. To boost the power of these association studies, we collected RNA-sequencing data from lymphoblastoid cell lines for 431 Hutterite individuals. We then used Sherlock, a tool that integrates GWAS and expression quantitative trait locus (eQTL) data, to identify weak GWAS signals that are also supported by eQTL data. Using this approach, we found novel associations with quantitative phenotypes related to cardiovascular disease, including carotid intima-media thickness, left atrial volume index, monocyte count and serum YKL-40 levels. |
format | Online Article Text |
id | pubmed-5062579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50625792016-10-14 Integrated analyses of gene expression and genetic association studies in a founder population Cusanovich, Darren A. Caliskan, Minal Billstrand, Christine Michelini, Katelyn Chavarria, Claudia De Leon, Sherryl Mitrano, Amy Lewellyn, Noah Elias, Jack A. Chupp, Geoffrey L. Lang, Roberto M. Shah, Sanjiv J. Decara, Jeanne M. Gilad, Yoav Ober, Carole Hum Mol Genet Association Studies Articles Genome-wide association studies (GWASs) have become a standard tool for dissecting genetic contributions to disease risk. However, these studies typically require extraordinarily large sample sizes to be adequately powered. Strategies that incorporate functional information alongside genetic associations have proved successful in increasing GWAS power. Following this paradigm, we present the results of 20 different genetic association studies for quantitative traits related to complex diseases, conducted in the Hutterites of South Dakota. To boost the power of these association studies, we collected RNA-sequencing data from lymphoblastoid cell lines for 431 Hutterite individuals. We then used Sherlock, a tool that integrates GWAS and expression quantitative trait locus (eQTL) data, to identify weak GWAS signals that are also supported by eQTL data. Using this approach, we found novel associations with quantitative phenotypes related to cardiovascular disease, including carotid intima-media thickness, left atrial volume index, monocyte count and serum YKL-40 levels. Oxford University Press 2016-05-15 2016-02-29 /pmc/articles/PMC5062579/ /pubmed/26931462 http://dx.doi.org/10.1093/hmg/ddw061 Text en © The Author 2016. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Association Studies Articles Cusanovich, Darren A. Caliskan, Minal Billstrand, Christine Michelini, Katelyn Chavarria, Claudia De Leon, Sherryl Mitrano, Amy Lewellyn, Noah Elias, Jack A. Chupp, Geoffrey L. Lang, Roberto M. Shah, Sanjiv J. Decara, Jeanne M. Gilad, Yoav Ober, Carole Integrated analyses of gene expression and genetic association studies in a founder population |
title | Integrated analyses of gene expression and genetic association studies in a founder population |
title_full | Integrated analyses of gene expression and genetic association studies in a founder population |
title_fullStr | Integrated analyses of gene expression and genetic association studies in a founder population |
title_full_unstemmed | Integrated analyses of gene expression and genetic association studies in a founder population |
title_short | Integrated analyses of gene expression and genetic association studies in a founder population |
title_sort | integrated analyses of gene expression and genetic association studies in a founder population |
topic | Association Studies Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062579/ https://www.ncbi.nlm.nih.gov/pubmed/26931462 http://dx.doi.org/10.1093/hmg/ddw061 |
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