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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...

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Detalles Bibliográficos
Autores principales: Pungpapong, Vitara, Wang, Libo, Lin, Yanzhu, Zhang, Dabao, Zhang, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
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.
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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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