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FHSA-SED: Two-Locus Model Detection for Genome-Wide Association Study with Harmony Search Algorithm
MOTIVATION: Two-locus model is a typical significant disease model to be identified in genome-wide association study (GWAS). Due to intensive computational burden and diversity of disease models, existing methods have drawbacks on low detection power, high computation cost, and preference for some t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807955/ https://www.ncbi.nlm.nih.gov/pubmed/27014873 http://dx.doi.org/10.1371/journal.pone.0150669 |
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author | Tuo, Shouheng Zhang, Junying Yuan, Xiguo Zhang, Yuanyuan Liu, Zhaowen |
author_facet | Tuo, Shouheng Zhang, Junying Yuan, Xiguo Zhang, Yuanyuan Liu, Zhaowen |
author_sort | Tuo, Shouheng |
collection | PubMed |
description | MOTIVATION: Two-locus model is a typical significant disease model to be identified in genome-wide association study (GWAS). Due to intensive computational burden and diversity of disease models, existing methods have drawbacks on low detection power, high computation cost, and preference for some types of disease models. METHOD: In this study, two scoring functions (Bayesian network based K2-score and Gini-score) are used for characterizing two SNP locus as a candidate model, the two criteria are adopted simultaneously for improving identification power and tackling the preference problem to disease models. Harmony search algorithm (HSA) is improved for quickly finding the most likely candidate models among all two-locus models, in which a local search algorithm with two-dimensional tabu table is presented to avoid repeatedly evaluating some disease models that have strong marginal effect. Finally G-test statistic is used to further test the candidate models. RESULTS: We investigate our method named FHSA-SED on 82 simulated datasets and a real AMD dataset, and compare it with two typical methods (MACOED and CSE) which have been developed recently based on swarm intelligent search algorithm. The results of simulation experiments indicate that our method outperforms the two compared algorithms in terms of detection power, computation time, evaluation times, sensitivity (TPR), specificity (SPC), positive predictive value (PPV) and accuracy (ACC). Our method has identified two SNPs (rs3775652 and rs10511467) that may be also associated with disease in AMD dataset. |
format | Online Article Text |
id | pubmed-4807955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48079552016-04-05 FHSA-SED: Two-Locus Model Detection for Genome-Wide Association Study with Harmony Search Algorithm Tuo, Shouheng Zhang, Junying Yuan, Xiguo Zhang, Yuanyuan Liu, Zhaowen PLoS One Research Article MOTIVATION: Two-locus model is a typical significant disease model to be identified in genome-wide association study (GWAS). Due to intensive computational burden and diversity of disease models, existing methods have drawbacks on low detection power, high computation cost, and preference for some types of disease models. METHOD: In this study, two scoring functions (Bayesian network based K2-score and Gini-score) are used for characterizing two SNP locus as a candidate model, the two criteria are adopted simultaneously for improving identification power and tackling the preference problem to disease models. Harmony search algorithm (HSA) is improved for quickly finding the most likely candidate models among all two-locus models, in which a local search algorithm with two-dimensional tabu table is presented to avoid repeatedly evaluating some disease models that have strong marginal effect. Finally G-test statistic is used to further test the candidate models. RESULTS: We investigate our method named FHSA-SED on 82 simulated datasets and a real AMD dataset, and compare it with two typical methods (MACOED and CSE) which have been developed recently based on swarm intelligent search algorithm. The results of simulation experiments indicate that our method outperforms the two compared algorithms in terms of detection power, computation time, evaluation times, sensitivity (TPR), specificity (SPC), positive predictive value (PPV) and accuracy (ACC). Our method has identified two SNPs (rs3775652 and rs10511467) that may be also associated with disease in AMD dataset. Public Library of Science 2016-03-25 /pmc/articles/PMC4807955/ /pubmed/27014873 http://dx.doi.org/10.1371/journal.pone.0150669 Text en © 2016 Tuo 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Tuo, Shouheng Zhang, Junying Yuan, Xiguo Zhang, Yuanyuan Liu, Zhaowen FHSA-SED: Two-Locus Model Detection for Genome-Wide Association Study with Harmony Search Algorithm |
title | FHSA-SED: Two-Locus Model Detection for Genome-Wide Association Study with Harmony Search Algorithm |
title_full | FHSA-SED: Two-Locus Model Detection for Genome-Wide Association Study with Harmony Search Algorithm |
title_fullStr | FHSA-SED: Two-Locus Model Detection for Genome-Wide Association Study with Harmony Search Algorithm |
title_full_unstemmed | FHSA-SED: Two-Locus Model Detection for Genome-Wide Association Study with Harmony Search Algorithm |
title_short | FHSA-SED: Two-Locus Model Detection for Genome-Wide Association Study with Harmony Search Algorithm |
title_sort | fhsa-sed: two-locus model detection for genome-wide association study with harmony search algorithm |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807955/ https://www.ncbi.nlm.nih.gov/pubmed/27014873 http://dx.doi.org/10.1371/journal.pone.0150669 |
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