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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...

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Autores principales: Akdemir, Deniz, Jannink, Jean-Luc, Isidro-Sánchez, Julio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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.
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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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