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Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection
Next-generation sequencing technologies enable us to explore rare functional variants. However, most current statistical techniques are too underpowered to capture signals of rare variants in genome-wide association studies. We propose a supervised coalescing of single-nucleotide polymorphisms to ob...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287887/ https://www.ncbi.nlm.nih.gov/pubmed/22373502 http://dx.doi.org/10.1186/1753-6561-5-S9-S5 |
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author | Pungpapong, Vitara Wang, Libo Lin, Yanzhu Zhang, Dabao Zhang, Min |
author_facet | Pungpapong, Vitara Wang, Libo Lin, Yanzhu Zhang, Dabao Zhang, Min |
author_sort | Pungpapong, Vitara |
collection | PubMed |
description | Next-generation sequencing technologies enable us to explore rare functional variants. However, most current statistical techniques are too underpowered to capture signals of rare variants in genome-wide association studies. We propose a supervised coalescing of single-nucleotide polymorphisms to obtain gene-based markers that can stably reveal possible genetic effects related to rare alleles. We use a newly developed empirical Bayes variable selection algorithm to identify associations between studied traits and genetic markers. Using our novel method, we analyzed the three continuous phenotypes in the GAW17 data set across 200 replicates, with intriguing results. |
format | Online Article Text |
id | pubmed-3287887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32878872012-02-28 Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection Pungpapong, Vitara Wang, Libo Lin, Yanzhu Zhang, Dabao Zhang, Min BMC Proc Proceedings Next-generation sequencing technologies enable us to explore rare functional variants. However, most current statistical techniques are too underpowered to capture signals of rare variants in genome-wide association studies. We propose a supervised coalescing of single-nucleotide polymorphisms to obtain gene-based markers that can stably reveal possible genetic effects related to rare alleles. We use a newly developed empirical Bayes variable selection algorithm to identify associations between studied traits and genetic markers. Using our novel method, we analyzed the three continuous phenotypes in the GAW17 data set across 200 replicates, with intriguing results. BioMed Central 2011-11-29 /pmc/articles/PMC3287887/ /pubmed/22373502 http://dx.doi.org/10.1186/1753-6561-5-S9-S5 Text en Copyright ©2011 Pungpapong 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. |
spellingShingle | Proceedings Pungpapong, Vitara Wang, Libo Lin, Yanzhu Zhang, Dabao Zhang, Min Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection |
title | Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection |
title_full | Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection |
title_fullStr | Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection |
title_full_unstemmed | Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection |
title_short | Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection |
title_sort | genome-wide association analysis of gaw17 data using an empirical bayes variable selection |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287887/ https://www.ncbi.nlm.nih.gov/pubmed/22373502 http://dx.doi.org/10.1186/1753-6561-5-S9-S5 |
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