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A pathway analysis applied to Genetic Analysis Workshop 16 genome-wide rheumatoid arthritis data
The identification of several hundred genomic regions affecting disease risk has proven the ability of genome-wide association studies have proven their ability to identify genetic contributors to disease. Currently, single-nucleotide polymorphism (SNP) association analysis is the most widely used m...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795995/ https://www.ncbi.nlm.nih.gov/pubmed/20018088 |
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author | Ballard, David H Aporntewan, Chatchawit Lee, Ji Young Lee, Joon Sang Wu, Zheyang Zhao, Hongyu |
author_facet | Ballard, David H Aporntewan, Chatchawit Lee, Ji Young Lee, Joon Sang Wu, Zheyang Zhao, Hongyu |
author_sort | Ballard, David H |
collection | PubMed |
description | The identification of several hundred genomic regions affecting disease risk has proven the ability of genome-wide association studies have proven their ability to identify genetic contributors to disease. Currently, single-nucleotide polymorphism (SNP) association analysis is the most widely used method of genome-wide association data, but recent research shows that multi-marker tests of association may provide greater power, especially when more than one mutation is present within a gene and the mutations are in low linkage disequilibrium with each other. Here we use a multi-marker association test based on regression to SNPs located within known genes to obtain a gene-level score of association. We then perform pathway analysis using this score as a measure of gene importance. We use two tests of pathway enrichment - a binomial test and a random set method. By utilizing publicly available gene and pathway information, we identify B cell, cytokine and inflammation response, and antigen presentation pathways as being associated with rheumatoid arthritis. These results confirm known biological mechanisms for auto-immunity disorders, of which rheumatoid arthritis is one. |
format | Text |
id | pubmed-2795995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27959952009-12-18 A pathway analysis applied to Genetic Analysis Workshop 16 genome-wide rheumatoid arthritis data Ballard, David H Aporntewan, Chatchawit Lee, Ji Young Lee, Joon Sang Wu, Zheyang Zhao, Hongyu BMC Proc Proceedings The identification of several hundred genomic regions affecting disease risk has proven the ability of genome-wide association studies have proven their ability to identify genetic contributors to disease. Currently, single-nucleotide polymorphism (SNP) association analysis is the most widely used method of genome-wide association data, but recent research shows that multi-marker tests of association may provide greater power, especially when more than one mutation is present within a gene and the mutations are in low linkage disequilibrium with each other. Here we use a multi-marker association test based on regression to SNPs located within known genes to obtain a gene-level score of association. We then perform pathway analysis using this score as a measure of gene importance. We use two tests of pathway enrichment - a binomial test and a random set method. By utilizing publicly available gene and pathway information, we identify B cell, cytokine and inflammation response, and antigen presentation pathways as being associated with rheumatoid arthritis. These results confirm known biological mechanisms for auto-immunity disorders, of which rheumatoid arthritis is one. BioMed Central 2009-12-15 /pmc/articles/PMC2795995/ /pubmed/20018088 Text en Copyright ©2009 Ballard 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 Ballard, David H Aporntewan, Chatchawit Lee, Ji Young Lee, Joon Sang Wu, Zheyang Zhao, Hongyu A pathway analysis applied to Genetic Analysis Workshop 16 genome-wide rheumatoid arthritis data |
title | A pathway analysis applied to Genetic Analysis Workshop 16 genome-wide rheumatoid arthritis data |
title_full | A pathway analysis applied to Genetic Analysis Workshop 16 genome-wide rheumatoid arthritis data |
title_fullStr | A pathway analysis applied to Genetic Analysis Workshop 16 genome-wide rheumatoid arthritis data |
title_full_unstemmed | A pathway analysis applied to Genetic Analysis Workshop 16 genome-wide rheumatoid arthritis data |
title_short | A pathway analysis applied to Genetic Analysis Workshop 16 genome-wide rheumatoid arthritis data |
title_sort | pathway analysis applied to genetic analysis workshop 16 genome-wide rheumatoid arthritis data |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795995/ https://www.ncbi.nlm.nih.gov/pubmed/20018088 |
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