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A weighted accumulation test for associating rare genetic variation with quantitative phenotypes
Currently there is a great deal of interest in developing methods for testing the role that rare variation plays in disease development. Here we propose a weighted association test that accumulates genetic variation across a signaling pathway. We evaluate our approach by analyzing simulated phenotyp...
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/PMC3287898/ https://www.ncbi.nlm.nih.gov/pubmed/22373271 http://dx.doi.org/10.1186/1753-6561-5-S9-S6 |
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author | Xing, Chuanhua Satten, Glen A Allen, Andrew S |
author_facet | Xing, Chuanhua Satten, Glen A Allen, Andrew S |
author_sort | Xing, Chuanhua |
collection | PubMed |
description | Currently there is a great deal of interest in developing methods for testing the role that rare variation plays in disease development. Here we propose a weighted association test that accumulates genetic variation across a signaling pathway. We evaluate our approach by analyzing simulated phenotype data from an exome sequencing study of 697 unrelated individuals from the Genetic Analysis Workshop 17 (GAW17) data set. Although our weighted approach identifies several interesting pathways associated with phenotype Q1, so does an alternative unweighted accumulation approach. Such a result is not unexpected because there is no systematic relationship between the allele frequency of a variant and its effect on phenotype in the GAW17 simulation model. |
format | Online Article Text |
id | pubmed-3287898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32878982012-02-28 A weighted accumulation test for associating rare genetic variation with quantitative phenotypes Xing, Chuanhua Satten, Glen A Allen, Andrew S BMC Proc Proceedings Currently there is a great deal of interest in developing methods for testing the role that rare variation plays in disease development. Here we propose a weighted association test that accumulates genetic variation across a signaling pathway. We evaluate our approach by analyzing simulated phenotype data from an exome sequencing study of 697 unrelated individuals from the Genetic Analysis Workshop 17 (GAW17) data set. Although our weighted approach identifies several interesting pathways associated with phenotype Q1, so does an alternative unweighted accumulation approach. Such a result is not unexpected because there is no systematic relationship between the allele frequency of a variant and its effect on phenotype in the GAW17 simulation model. BioMed Central 2011-11-29 /pmc/articles/PMC3287898/ /pubmed/22373271 http://dx.doi.org/10.1186/1753-6561-5-S9-S6 Text en Copyright ©2011 Xing 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 Xing, Chuanhua Satten, Glen A Allen, Andrew S A weighted accumulation test for associating rare genetic variation with quantitative phenotypes |
title | A weighted accumulation test for associating rare genetic variation with quantitative phenotypes |
title_full | A weighted accumulation test for associating rare genetic variation with quantitative phenotypes |
title_fullStr | A weighted accumulation test for associating rare genetic variation with quantitative phenotypes |
title_full_unstemmed | A weighted accumulation test for associating rare genetic variation with quantitative phenotypes |
title_short | A weighted accumulation test for associating rare genetic variation with quantitative phenotypes |
title_sort | weighted accumulation test for associating rare genetic variation with quantitative phenotypes |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287898/ https://www.ncbi.nlm.nih.gov/pubmed/22373271 http://dx.doi.org/10.1186/1753-6561-5-S9-S6 |
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