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Identifying rare variants from exome scans: the GAW17 experience
Genetic Analysis Workshop 17 (GAW17) provided a platform for evaluating existing statistical genetic methods and for developing novel methods to analyze rare variants that modulate complex traits. In this article, we present an overview of the 1000 Genomes Project exome data and simulated phenotype...
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/PMC3287821/ https://www.ncbi.nlm.nih.gov/pubmed/22373325 http://dx.doi.org/10.1186/1753-6561-5-S9-S1 |
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author | Ghosh, Saurabh Bickeböller, Heike Bailey, Julia Bailey-Wilson, Joan E Cantor, Rita Culverhouse, Robert Daw, Warwick DeStefano, Anita L Engelman, Corinne D Hinrichs, Anthony Houwing-Duistermaat, Jeanine König, Inke R Kent, Jack Laird, Nan Pankratz, Nathan Paterson, Andrew Pugh, Elizabeth Suarez, Brian Sun, Yan Thomas, Alun Tintle, Nathan Zhu, Xiaofeng Ziegler, Andreas MacCluer, Jean W Almasy, Laura |
author_facet | Ghosh, Saurabh Bickeböller, Heike Bailey, Julia Bailey-Wilson, Joan E Cantor, Rita Culverhouse, Robert Daw, Warwick DeStefano, Anita L Engelman, Corinne D Hinrichs, Anthony Houwing-Duistermaat, Jeanine König, Inke R Kent, Jack Laird, Nan Pankratz, Nathan Paterson, Andrew Pugh, Elizabeth Suarez, Brian Sun, Yan Thomas, Alun Tintle, Nathan Zhu, Xiaofeng Ziegler, Andreas MacCluer, Jean W Almasy, Laura |
author_sort | Ghosh, Saurabh |
collection | PubMed |
description | Genetic Analysis Workshop 17 (GAW17) provided a platform for evaluating existing statistical genetic methods and for developing novel methods to analyze rare variants that modulate complex traits. In this article, we present an overview of the 1000 Genomes Project exome data and simulated phenotype data that were distributed to GAW17 participants for analyses, the different issues addressed by the participants, and the process of preparation of manuscripts resulting from the discussions during the workshop. |
format | Online Article Text |
id | pubmed-3287821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32878212012-02-28 Identifying rare variants from exome scans: the GAW17 experience Ghosh, Saurabh Bickeböller, Heike Bailey, Julia Bailey-Wilson, Joan E Cantor, Rita Culverhouse, Robert Daw, Warwick DeStefano, Anita L Engelman, Corinne D Hinrichs, Anthony Houwing-Duistermaat, Jeanine König, Inke R Kent, Jack Laird, Nan Pankratz, Nathan Paterson, Andrew Pugh, Elizabeth Suarez, Brian Sun, Yan Thomas, Alun Tintle, Nathan Zhu, Xiaofeng Ziegler, Andreas MacCluer, Jean W Almasy, Laura BMC Proc Proceedings Genetic Analysis Workshop 17 (GAW17) provided a platform for evaluating existing statistical genetic methods and for developing novel methods to analyze rare variants that modulate complex traits. In this article, we present an overview of the 1000 Genomes Project exome data and simulated phenotype data that were distributed to GAW17 participants for analyses, the different issues addressed by the participants, and the process of preparation of manuscripts resulting from the discussions during the workshop. BioMed Central 2011-11-29 /pmc/articles/PMC3287821/ /pubmed/22373325 http://dx.doi.org/10.1186/1753-6561-5-S9-S1 Text en Copyright ©2011 Ghosh 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 Ghosh, Saurabh Bickeböller, Heike Bailey, Julia Bailey-Wilson, Joan E Cantor, Rita Culverhouse, Robert Daw, Warwick DeStefano, Anita L Engelman, Corinne D Hinrichs, Anthony Houwing-Duistermaat, Jeanine König, Inke R Kent, Jack Laird, Nan Pankratz, Nathan Paterson, Andrew Pugh, Elizabeth Suarez, Brian Sun, Yan Thomas, Alun Tintle, Nathan Zhu, Xiaofeng Ziegler, Andreas MacCluer, Jean W Almasy, Laura Identifying rare variants from exome scans: the GAW17 experience |
title | Identifying rare variants from exome scans: the GAW17 experience |
title_full | Identifying rare variants from exome scans: the GAW17 experience |
title_fullStr | Identifying rare variants from exome scans: the GAW17 experience |
title_full_unstemmed | Identifying rare variants from exome scans: the GAW17 experience |
title_short | Identifying rare variants from exome scans: the GAW17 experience |
title_sort | identifying rare variants from exome scans: the gaw17 experience |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287821/ https://www.ncbi.nlm.nih.gov/pubmed/22373325 http://dx.doi.org/10.1186/1753-6561-5-S9-S1 |
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