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Locally epistatic models for genome-wide prediction and association by importance sampling
BACKGROUND: In statistical genetics, an important task involves building predictive models of the genotype–phenotype relationship to attribute a proportion of the total phenotypic variance to the variation in genotypes. Many models have been proposed to incorporate additive genetic effects into pred...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5646165/ https://www.ncbi.nlm.nih.gov/pubmed/29041917 http://dx.doi.org/10.1186/s12711-017-0348-8 |
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author | Akdemir, Deniz Jannink, Jean-Luc Isidro-Sánchez, Julio |
author_facet | Akdemir, Deniz Jannink, Jean-Luc Isidro-Sánchez, Julio |
author_sort | Akdemir, Deniz |
collection | PubMed |
description | BACKGROUND: In statistical genetics, an important task involves building predictive models of the genotype–phenotype relationship to attribute a proportion of the total phenotypic variance to the variation in genotypes. Many models have been proposed to incorporate additive genetic effects into prediction or association models. Currently, there is a scarcity of models that can adequately account for gene by gene or other forms of genetic interactions, and there is an increased interest in using marker annotations in genome-wide prediction and association analyses. In this paper, we discuss a hybrid modeling method which combines parametric mixed modeling and non-parametric rule ensembles. RESULTS: This approach gives us a flexible class of models that can be used to capture additive, locally epistatic genetic effects, gene-by-background interactions and allows us to incorporate one or more annotations into the genomic selection or association models. We use benchmark datasets that cover a range of organisms and traits in addition to simulated datasets to illustrate the strengths of this approach. CONCLUSIONS: In this paper, we describe a new strategy for incorporating genetic interactions into genomic prediction and association models. This strategy results in accurate models, with sometimes significantly higher accuracies than that of a standard additive model. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12711-017-0348-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5646165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56461652017-10-26 Locally epistatic models for genome-wide prediction and association by importance sampling Akdemir, Deniz Jannink, Jean-Luc Isidro-Sánchez, Julio Genet Sel Evol Research Article BACKGROUND: In statistical genetics, an important task involves building predictive models of the genotype–phenotype relationship to attribute a proportion of the total phenotypic variance to the variation in genotypes. Many models have been proposed to incorporate additive genetic effects into prediction or association models. Currently, there is a scarcity of models that can adequately account for gene by gene or other forms of genetic interactions, and there is an increased interest in using marker annotations in genome-wide prediction and association analyses. In this paper, we discuss a hybrid modeling method which combines parametric mixed modeling and non-parametric rule ensembles. RESULTS: This approach gives us a flexible class of models that can be used to capture additive, locally epistatic genetic effects, gene-by-background interactions and allows us to incorporate one or more annotations into the genomic selection or association models. We use benchmark datasets that cover a range of organisms and traits in addition to simulated datasets to illustrate the strengths of this approach. CONCLUSIONS: In this paper, we describe a new strategy for incorporating genetic interactions into genomic prediction and association models. This strategy results in accurate models, with sometimes significantly higher accuracies than that of a standard additive model. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12711-017-0348-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-17 /pmc/articles/PMC5646165/ /pubmed/29041917 http://dx.doi.org/10.1186/s12711-017-0348-8 Text en © The Author(s) 2017 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 Article Akdemir, Deniz Jannink, Jean-Luc Isidro-Sánchez, Julio Locally epistatic models for genome-wide prediction and association by importance sampling |
title | Locally epistatic models for genome-wide prediction and association by importance sampling |
title_full | Locally epistatic models for genome-wide prediction and association by importance sampling |
title_fullStr | Locally epistatic models for genome-wide prediction and association by importance sampling |
title_full_unstemmed | Locally epistatic models for genome-wide prediction and association by importance sampling |
title_short | Locally epistatic models for genome-wide prediction and association by importance sampling |
title_sort | locally epistatic models for genome-wide prediction and association by importance sampling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5646165/ https://www.ncbi.nlm.nih.gov/pubmed/29041917 http://dx.doi.org/10.1186/s12711-017-0348-8 |
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