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Fuzzy set-based generalized multifactor dimensionality reduction analysis of gene-gene interactions
BACKGROUND: Gene-gene interactions (GGIs) are a known cause of missing heritability. Multifactor dimensionality reduction (MDR) is one of most commonly used methods for GGI detection. The generalized multifactor dimensionality reduction (GMDR) method is an extension of MDR method that is applicable...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918459/ https://www.ncbi.nlm.nih.gov/pubmed/29697366 http://dx.doi.org/10.1186/s12920-018-0343-0 |
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author | Jung, Hye-Young Leem, Sangseob Park, Taesung |
author_facet | Jung, Hye-Young Leem, Sangseob Park, Taesung |
author_sort | Jung, Hye-Young |
collection | PubMed |
description | BACKGROUND: Gene-gene interactions (GGIs) are a known cause of missing heritability. Multifactor dimensionality reduction (MDR) is one of most commonly used methods for GGI detection. The generalized multifactor dimensionality reduction (GMDR) method is an extension of MDR method that is applicable to various types of traits, and allows covariate adjustments. Our previous Fuzzy MDR (FMDR) is another extension for overcoming simple binary classification. FMDR uses continuous member-ship values instead of binary membership values 0 and 1, improving power for detecting causal SNPs and more intuitive interpretations in real data analysis. Here, we propose the fuzzy generalized multifactor dimensionality reduction (FGMDR) method, as a combined analysis of fuzzy set-based analysis and GMDR method, to detect GGIs associated with diseases using fuzzy set theory. RESULTS: Through simulation studies for different types of traits, the proposed FGMDR showed a higher detection ratio of causal SNPs, compared to GMDR. We then applied FGMDR to two real data: Crohn’s disease (CD) data from the Wellcome Trust Case Control Consortium (WTCCC) with a binary phenotype and the Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) data from Korean population with a continuous phenotype. The interactions derived by our method include the pre-reported interactions associated with phenotypes. CONCLUSIONS: The proposed FGMDR performs well for GGI detection with covariate adjustments. The program written in R for FGMDR is available at http://statgen.snu.ac.kr/software/FGMDR. |
format | Online Article Text |
id | pubmed-5918459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59184592018-04-30 Fuzzy set-based generalized multifactor dimensionality reduction analysis of gene-gene interactions Jung, Hye-Young Leem, Sangseob Park, Taesung BMC Med Genomics Research BACKGROUND: Gene-gene interactions (GGIs) are a known cause of missing heritability. Multifactor dimensionality reduction (MDR) is one of most commonly used methods for GGI detection. The generalized multifactor dimensionality reduction (GMDR) method is an extension of MDR method that is applicable to various types of traits, and allows covariate adjustments. Our previous Fuzzy MDR (FMDR) is another extension for overcoming simple binary classification. FMDR uses continuous member-ship values instead of binary membership values 0 and 1, improving power for detecting causal SNPs and more intuitive interpretations in real data analysis. Here, we propose the fuzzy generalized multifactor dimensionality reduction (FGMDR) method, as a combined analysis of fuzzy set-based analysis and GMDR method, to detect GGIs associated with diseases using fuzzy set theory. RESULTS: Through simulation studies for different types of traits, the proposed FGMDR showed a higher detection ratio of causal SNPs, compared to GMDR. We then applied FGMDR to two real data: Crohn’s disease (CD) data from the Wellcome Trust Case Control Consortium (WTCCC) with a binary phenotype and the Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) data from Korean population with a continuous phenotype. The interactions derived by our method include the pre-reported interactions associated with phenotypes. CONCLUSIONS: The proposed FGMDR performs well for GGI detection with covariate adjustments. The program written in R for FGMDR is available at http://statgen.snu.ac.kr/software/FGMDR. BioMed Central 2018-04-20 /pmc/articles/PMC5918459/ /pubmed/29697366 http://dx.doi.org/10.1186/s12920-018-0343-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Jung, Hye-Young Leem, Sangseob Park, Taesung Fuzzy set-based generalized multifactor dimensionality reduction analysis of gene-gene interactions |
title | Fuzzy set-based generalized multifactor dimensionality reduction analysis of gene-gene interactions |
title_full | Fuzzy set-based generalized multifactor dimensionality reduction analysis of gene-gene interactions |
title_fullStr | Fuzzy set-based generalized multifactor dimensionality reduction analysis of gene-gene interactions |
title_full_unstemmed | Fuzzy set-based generalized multifactor dimensionality reduction analysis of gene-gene interactions |
title_short | Fuzzy set-based generalized multifactor dimensionality reduction analysis of gene-gene interactions |
title_sort | fuzzy set-based generalized multifactor dimensionality reduction analysis of gene-gene interactions |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918459/ https://www.ncbi.nlm.nih.gov/pubmed/29697366 http://dx.doi.org/10.1186/s12920-018-0343-0 |
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