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Identification of multiple gene-gene interactions for ordinal phenotypes

BACKGROUND: Multifactor dimensionality reduction (MDR) is a powerful method for analysis of gene-gene interactions and has been successfully applied to many genetic studies of complex diseases. However, the main application of MDR has been limited to binary traits, while traits having ordinal featur...

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Autores principales: Kim, Kyunga, Kwon, Min-Seok, Oh, Sohee, Park, Taesung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654913/
https://www.ncbi.nlm.nih.gov/pubmed/23819572
http://dx.doi.org/10.1186/1755-8794-6-S2-S9
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author Kim, Kyunga
Kwon, Min-Seok
Oh, Sohee
Park, Taesung
author_facet Kim, Kyunga
Kwon, Min-Seok
Oh, Sohee
Park, Taesung
author_sort Kim, Kyunga
collection PubMed
description BACKGROUND: Multifactor dimensionality reduction (MDR) is a powerful method for analysis of gene-gene interactions and has been successfully applied to many genetic studies of complex diseases. However, the main application of MDR has been limited to binary traits, while traits having ordinal features are commonly observed in many genetic studies (e.g., obesity classification - normal, pre-obese, mild obese and severe obese). METHODS: We propose ordinal MDR (OMDR) to facilitate gene-gene interaction analysis for ordinal traits. As an alternative to balanced accuracy, the use of tau-b, a common ordinal association measure, was suggested to evaluate interactions. Also, we generalized cross-validation consistency (GCVC) to identify multiple best interactions. GCVC can be practically useful for analyzing complex traits, especially in large-scale genetic studies. RESULTS AND CONCLUSIONS: In simulations, OMDR showed fairly good performance in terms of power, predictability and selection stability and outperformed MDR. For demonstration, we used a real data of body mass index (BMI) and scanned 1~4-way interactions of obesity ordinal and binary traits of BMI via OMDR and MDR, respectively. In real data analysis, more interactions were identified for ordinal trait than binary traits. On average, the commonly identified interactions showed higher predictability for ordinal trait than binary traits. The proposed OMDR and GCVC were implemented in a C/C++ program, executables of which are freely available for Linux, Windows and MacOS upon request for non-commercial research institutions.
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spelling pubmed-36549132013-05-20 Identification of multiple gene-gene interactions for ordinal phenotypes Kim, Kyunga Kwon, Min-Seok Oh, Sohee Park, Taesung BMC Med Genomics Research BACKGROUND: Multifactor dimensionality reduction (MDR) is a powerful method for analysis of gene-gene interactions and has been successfully applied to many genetic studies of complex diseases. However, the main application of MDR has been limited to binary traits, while traits having ordinal features are commonly observed in many genetic studies (e.g., obesity classification - normal, pre-obese, mild obese and severe obese). METHODS: We propose ordinal MDR (OMDR) to facilitate gene-gene interaction analysis for ordinal traits. As an alternative to balanced accuracy, the use of tau-b, a common ordinal association measure, was suggested to evaluate interactions. Also, we generalized cross-validation consistency (GCVC) to identify multiple best interactions. GCVC can be practically useful for analyzing complex traits, especially in large-scale genetic studies. RESULTS AND CONCLUSIONS: In simulations, OMDR showed fairly good performance in terms of power, predictability and selection stability and outperformed MDR. For demonstration, we used a real data of body mass index (BMI) and scanned 1~4-way interactions of obesity ordinal and binary traits of BMI via OMDR and MDR, respectively. In real data analysis, more interactions were identified for ordinal trait than binary traits. On average, the commonly identified interactions showed higher predictability for ordinal trait than binary traits. The proposed OMDR and GCVC were implemented in a C/C++ program, executables of which are freely available for Linux, Windows and MacOS upon request for non-commercial research institutions. BioMed Central 2013-05-07 /pmc/articles/PMC3654913/ /pubmed/23819572 http://dx.doi.org/10.1186/1755-8794-6-S2-S9 Text en Copyright © 2013 Kim 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 Research
Kim, Kyunga
Kwon, Min-Seok
Oh, Sohee
Park, Taesung
Identification of multiple gene-gene interactions for ordinal phenotypes
title Identification of multiple gene-gene interactions for ordinal phenotypes
title_full Identification of multiple gene-gene interactions for ordinal phenotypes
title_fullStr Identification of multiple gene-gene interactions for ordinal phenotypes
title_full_unstemmed Identification of multiple gene-gene interactions for ordinal phenotypes
title_short Identification of multiple gene-gene interactions for ordinal phenotypes
title_sort identification of multiple gene-gene interactions for ordinal phenotypes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654913/
https://www.ncbi.nlm.nih.gov/pubmed/23819572
http://dx.doi.org/10.1186/1755-8794-6-S2-S9
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