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A hidden two-locus disease association pattern in genome-wide association studies

BACKGROUND: Recent association analyses in genome-wide association studies (GWAS) mainly focus on single-locus association tests (marginal tests) and two-locus interaction detections. These analysis methods have provided strong evidence of associations between genetics variances and complex diseases...

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Autores principales: Yang, Can, Wan, Xiang, Yang, Qiang, Xue, Hong, Tang, Nelson LS, Yu, Weichuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3116488/
https://www.ncbi.nlm.nih.gov/pubmed/21569557
http://dx.doi.org/10.1186/1471-2105-12-156
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author Yang, Can
Wan, Xiang
Yang, Qiang
Xue, Hong
Tang, Nelson LS
Yu, Weichuan
author_facet Yang, Can
Wan, Xiang
Yang, Qiang
Xue, Hong
Tang, Nelson LS
Yu, Weichuan
author_sort Yang, Can
collection PubMed
description BACKGROUND: Recent association analyses in genome-wide association studies (GWAS) mainly focus on single-locus association tests (marginal tests) and two-locus interaction detections. These analysis methods have provided strong evidence of associations between genetics variances and complex diseases. However, there exists a type of association pattern, which often occurs within local regions in the genome and is unlikely to be detected by either marginal tests or interaction tests. This association pattern involves a group of correlated single-nucleotide polymorphisms (SNPs). The correlation among SNPs can lead to weak marginal effects and the interaction does not play a role in this association pattern. This phenomenon is due to the existence of unfaithfulness: the marginal effects of correlated SNPs do not express their significant joint effects faithfully due to the correlation cancelation. RESULTS: In this paper, we develop a computational method to detect this association pattern masked by unfaithfulness. We have applied our method to analyze seven data sets from the Wellcome Trust Case Control Consortium (WTCCC). The analysis for each data set takes about one week to finish the examination of all pairs of SNPs. Based on the empirical result of these real data, we show that this type of association masked by unfaithfulness widely exists in GWAS. CONCLUSIONS: These newly identified associations enrich the discoveries of GWAS, which may provide new insights both in the analysis of tagSNPs and in the experiment design of GWAS. Since these associations may be easily missed by existing analysis tools, we can only connect some of them to publicly available findings from other association studies. As independent data set is limited at this moment, we also have difficulties to replicate these findings. More biological implications need further investigation. AVAILABILITY: The software is freely available at http://bioinformatics.ust.hk/hidden_pattern_finder.zip.
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spelling pubmed-31164882011-06-17 A hidden two-locus disease association pattern in genome-wide association studies Yang, Can Wan, Xiang Yang, Qiang Xue, Hong Tang, Nelson LS Yu, Weichuan BMC Bioinformatics Methodology Article BACKGROUND: Recent association analyses in genome-wide association studies (GWAS) mainly focus on single-locus association tests (marginal tests) and two-locus interaction detections. These analysis methods have provided strong evidence of associations between genetics variances and complex diseases. However, there exists a type of association pattern, which often occurs within local regions in the genome and is unlikely to be detected by either marginal tests or interaction tests. This association pattern involves a group of correlated single-nucleotide polymorphisms (SNPs). The correlation among SNPs can lead to weak marginal effects and the interaction does not play a role in this association pattern. This phenomenon is due to the existence of unfaithfulness: the marginal effects of correlated SNPs do not express their significant joint effects faithfully due to the correlation cancelation. RESULTS: In this paper, we develop a computational method to detect this association pattern masked by unfaithfulness. We have applied our method to analyze seven data sets from the Wellcome Trust Case Control Consortium (WTCCC). The analysis for each data set takes about one week to finish the examination of all pairs of SNPs. Based on the empirical result of these real data, we show that this type of association masked by unfaithfulness widely exists in GWAS. CONCLUSIONS: These newly identified associations enrich the discoveries of GWAS, which may provide new insights both in the analysis of tagSNPs and in the experiment design of GWAS. Since these associations may be easily missed by existing analysis tools, we can only connect some of them to publicly available findings from other association studies. As independent data set is limited at this moment, we also have difficulties to replicate these findings. More biological implications need further investigation. AVAILABILITY: The software is freely available at http://bioinformatics.ust.hk/hidden_pattern_finder.zip. BioMed Central 2011-05-14 /pmc/articles/PMC3116488/ /pubmed/21569557 http://dx.doi.org/10.1186/1471-2105-12-156 Text en Copyright ©2011 Yang 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 Methodology Article
Yang, Can
Wan, Xiang
Yang, Qiang
Xue, Hong
Tang, Nelson LS
Yu, Weichuan
A hidden two-locus disease association pattern in genome-wide association studies
title A hidden two-locus disease association pattern in genome-wide association studies
title_full A hidden two-locus disease association pattern in genome-wide association studies
title_fullStr A hidden two-locus disease association pattern in genome-wide association studies
title_full_unstemmed A hidden two-locus disease association pattern in genome-wide association studies
title_short A hidden two-locus disease association pattern in genome-wide association studies
title_sort hidden two-locus disease association pattern in genome-wide association studies
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3116488/
https://www.ncbi.nlm.nih.gov/pubmed/21569557
http://dx.doi.org/10.1186/1471-2105-12-156
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