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iLOCi: a SNP interaction prioritization technique for detecting epistasis in genome-wide association studies

BACKGROUND: Genome-wide association studies (GWAS) do not provide a full account of the heritability of genetic diseases since gene-gene interactions, also known as epistasis are not considered in single locus GWAS. To address this problem, a considerable number of methods have been developed for id...

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Autores principales: Piriyapongsa, Jittima, Ngamphiw, Chumpol, Intarapanich, Apichart, Kulawonganunchai, Supasak, Assawamakin, Anunchai, Bootchai, Chaiwat, Shaw, Philip J, Tongsima, Sissades
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521387/
https://www.ncbi.nlm.nih.gov/pubmed/23281813
http://dx.doi.org/10.1186/1471-2164-13-S7-S2
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author Piriyapongsa, Jittima
Ngamphiw, Chumpol
Intarapanich, Apichart
Kulawonganunchai, Supasak
Assawamakin, Anunchai
Bootchai, Chaiwat
Shaw, Philip J
Tongsima, Sissades
author_facet Piriyapongsa, Jittima
Ngamphiw, Chumpol
Intarapanich, Apichart
Kulawonganunchai, Supasak
Assawamakin, Anunchai
Bootchai, Chaiwat
Shaw, Philip J
Tongsima, Sissades
author_sort Piriyapongsa, Jittima
collection PubMed
description BACKGROUND: Genome-wide association studies (GWAS) do not provide a full account of the heritability of genetic diseases since gene-gene interactions, also known as epistasis are not considered in single locus GWAS. To address this problem, a considerable number of methods have been developed for identifying disease-associated gene-gene interactions. However, these methods typically fail to identify interacting markers explaining more of the disease heritability over single locus GWAS, since many of the interactions significant for disease are obscured by uninformative marker interactions e.g., linkage disequilibrium (LD). RESULTS: In this study, we present a novel SNP interaction prioritization algorithm, named iLOCi (Interacting Loci). This algorithm accounts for marker dependencies separately in case and control groups. Disease-associated interactions are then prioritized according to a novel ranking score calculated from the difference in marker dependencies for every possible pair between case and control groups. The analysis of a typical GWAS dataset can be completed in less than a day on a standard workstation with parallel processing capability. The proposed framework was validated using simulated data and applied to real GWAS datasets using the Wellcome Trust Case Control Consortium (WTCCC) data. The results from simulated data showed the ability of iLOCi to identify various types of gene-gene interactions, especially for high-order interaction. From the WTCCC data, we found that among the top ranked interacting SNP pairs, several mapped to genes previously known to be associated with disease, and interestingly, other previously unreported genes with biologically related roles. CONCLUSION: iLOCi is a powerful tool for uncovering true disease interacting markers and thus can provide a more complete understanding of the genetic basis underlying complex disease. The program is available for download at http://www4a.biotec.or.th/GI/tools/iloci.
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spelling pubmed-35213872012-12-14 iLOCi: a SNP interaction prioritization technique for detecting epistasis in genome-wide association studies Piriyapongsa, Jittima Ngamphiw, Chumpol Intarapanich, Apichart Kulawonganunchai, Supasak Assawamakin, Anunchai Bootchai, Chaiwat Shaw, Philip J Tongsima, Sissades BMC Genomics Proceedings BACKGROUND: Genome-wide association studies (GWAS) do not provide a full account of the heritability of genetic diseases since gene-gene interactions, also known as epistasis are not considered in single locus GWAS. To address this problem, a considerable number of methods have been developed for identifying disease-associated gene-gene interactions. However, these methods typically fail to identify interacting markers explaining more of the disease heritability over single locus GWAS, since many of the interactions significant for disease are obscured by uninformative marker interactions e.g., linkage disequilibrium (LD). RESULTS: In this study, we present a novel SNP interaction prioritization algorithm, named iLOCi (Interacting Loci). This algorithm accounts for marker dependencies separately in case and control groups. Disease-associated interactions are then prioritized according to a novel ranking score calculated from the difference in marker dependencies for every possible pair between case and control groups. The analysis of a typical GWAS dataset can be completed in less than a day on a standard workstation with parallel processing capability. The proposed framework was validated using simulated data and applied to real GWAS datasets using the Wellcome Trust Case Control Consortium (WTCCC) data. The results from simulated data showed the ability of iLOCi to identify various types of gene-gene interactions, especially for high-order interaction. From the WTCCC data, we found that among the top ranked interacting SNP pairs, several mapped to genes previously known to be associated with disease, and interestingly, other previously unreported genes with biologically related roles. CONCLUSION: iLOCi is a powerful tool for uncovering true disease interacting markers and thus can provide a more complete understanding of the genetic basis underlying complex disease. The program is available for download at http://www4a.biotec.or.th/GI/tools/iloci. BioMed Central 2012-12-07 /pmc/articles/PMC3521387/ /pubmed/23281813 http://dx.doi.org/10.1186/1471-2164-13-S7-S2 Text en Copyright ©2012 Piriyapongsa 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
Piriyapongsa, Jittima
Ngamphiw, Chumpol
Intarapanich, Apichart
Kulawonganunchai, Supasak
Assawamakin, Anunchai
Bootchai, Chaiwat
Shaw, Philip J
Tongsima, Sissades
iLOCi: a SNP interaction prioritization technique for detecting epistasis in genome-wide association studies
title iLOCi: a SNP interaction prioritization technique for detecting epistasis in genome-wide association studies
title_full iLOCi: a SNP interaction prioritization technique for detecting epistasis in genome-wide association studies
title_fullStr iLOCi: a SNP interaction prioritization technique for detecting epistasis in genome-wide association studies
title_full_unstemmed iLOCi: a SNP interaction prioritization technique for detecting epistasis in genome-wide association studies
title_short iLOCi: a SNP interaction prioritization technique for detecting epistasis in genome-wide association studies
title_sort iloci: a snp interaction prioritization technique for detecting epistasis in genome-wide association studies
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521387/
https://www.ncbi.nlm.nih.gov/pubmed/23281813
http://dx.doi.org/10.1186/1471-2164-13-S7-S2
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