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From SNPs to Genes: Disease Association at the Gene Level

Interpreting Genome-Wide Association Studies (GWAS) at a gene level is an important step towards understanding the molecular processes that lead to disease. In order to incorporate prior biological knowledge such as pathways and protein interactions in the analysis of GWAS data it is necessary to de...

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Detalles Bibliográficos
Autores principales: Lehne, Benjamin, Lewis, Cathryn M., Schlitt, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128073/
https://www.ncbi.nlm.nih.gov/pubmed/21738570
http://dx.doi.org/10.1371/journal.pone.0020133
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author Lehne, Benjamin
Lewis, Cathryn M.
Schlitt, Thomas
author_facet Lehne, Benjamin
Lewis, Cathryn M.
Schlitt, Thomas
author_sort Lehne, Benjamin
collection PubMed
description Interpreting Genome-Wide Association Studies (GWAS) at a gene level is an important step towards understanding the molecular processes that lead to disease. In order to incorporate prior biological knowledge such as pathways and protein interactions in the analysis of GWAS data it is necessary to derive one measure of association for each gene. We compare three different methods to obtain gene-wide test statistics from Single Nucleotide Polymorphism (SNP) based association data: choosing the test statistic from the most significant SNP; the mean test statistics of all SNPs; and the mean of the top quartile of all test statistics. We demonstrate that the gene-wide test statistics can be controlled for the number of SNPs within each gene and show that all three methods perform considerably better than expected by chance at identifying genes with confirmed associations. By applying each method to GWAS data for Crohn's Disease and Type 1 Diabetes we identified new potential disease genes.
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spelling pubmed-31280732011-07-07 From SNPs to Genes: Disease Association at the Gene Level Lehne, Benjamin Lewis, Cathryn M. Schlitt, Thomas PLoS One Research Article Interpreting Genome-Wide Association Studies (GWAS) at a gene level is an important step towards understanding the molecular processes that lead to disease. In order to incorporate prior biological knowledge such as pathways and protein interactions in the analysis of GWAS data it is necessary to derive one measure of association for each gene. We compare three different methods to obtain gene-wide test statistics from Single Nucleotide Polymorphism (SNP) based association data: choosing the test statistic from the most significant SNP; the mean test statistics of all SNPs; and the mean of the top quartile of all test statistics. We demonstrate that the gene-wide test statistics can be controlled for the number of SNPs within each gene and show that all three methods perform considerably better than expected by chance at identifying genes with confirmed associations. By applying each method to GWAS data for Crohn's Disease and Type 1 Diabetes we identified new potential disease genes. Public Library of Science 2011-06-30 /pmc/articles/PMC3128073/ /pubmed/21738570 http://dx.doi.org/10.1371/journal.pone.0020133 Text en Lehne et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lehne, Benjamin
Lewis, Cathryn M.
Schlitt, Thomas
From SNPs to Genes: Disease Association at the Gene Level
title From SNPs to Genes: Disease Association at the Gene Level
title_full From SNPs to Genes: Disease Association at the Gene Level
title_fullStr From SNPs to Genes: Disease Association at the Gene Level
title_full_unstemmed From SNPs to Genes: Disease Association at the Gene Level
title_short From SNPs to Genes: Disease Association at the Gene Level
title_sort from snps to genes: disease association at the gene level
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128073/
https://www.ncbi.nlm.nih.gov/pubmed/21738570
http://dx.doi.org/10.1371/journal.pone.0020133
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