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A novel linkage-disequilibrium corrected genomic relationship matrix for SNP-heritability estimation and genomic prediction

Single nucleotide polymorphism (SNP)-heritability estimation is an important topic in several research fields, including animal, plant and human genetics, as well as in ecology. Linear mixed model estimation of SNP-heritability uses the structures of genomic relationships between individuals, which...

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Autores principales: Mathew, Boby, Léon, Jens, Sillanpää, Mikko J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842222/
https://www.ncbi.nlm.nih.gov/pubmed/29238077
http://dx.doi.org/10.1038/s41437-017-0023-4
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author Mathew, Boby
Léon, Jens
Sillanpää, Mikko J.
author_facet Mathew, Boby
Léon, Jens
Sillanpää, Mikko J.
author_sort Mathew, Boby
collection PubMed
description Single nucleotide polymorphism (SNP)-heritability estimation is an important topic in several research fields, including animal, plant and human genetics, as well as in ecology. Linear mixed model estimation of SNP-heritability uses the structures of genomic relationships between individuals, which is constructed from genome-wide sets of SNP-markers that are generally weighted equally in their contributions. Proposed methods to handle dependence between SNPs include, “thinning” the marker set by linkage disequilibrium (LD)-pruning, the use of haplotype-tagging of SNPs, and LD-weighting of the SNP-contributions. For improved estimation, we propose a new conceptual framework for genomic relationship matrix, in which Mahalanobis distance-based LD-correction is used in a linear mixed model estimation of SNP-heritability. The superiority of the presented method is illustrated and compared to mixed-model analyses using a VanRaden genomic relationship matrix, a matrix used by GCTA and a matrix employing LD-weighting (as implemented in the LDAK software) in simulated (using real human, rice and cattle genotypes) and real (maize, rice and mice) datasets. Despite of the computational difficulties, our results suggest that by using the proposed method one can improve the accuracy of SNP-heritability estimates in datasets with high LD.
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spelling pubmed-58422222018-04-24 A novel linkage-disequilibrium corrected genomic relationship matrix for SNP-heritability estimation and genomic prediction Mathew, Boby Léon, Jens Sillanpää, Mikko J. Heredity (Edinb) Article Single nucleotide polymorphism (SNP)-heritability estimation is an important topic in several research fields, including animal, plant and human genetics, as well as in ecology. Linear mixed model estimation of SNP-heritability uses the structures of genomic relationships between individuals, which is constructed from genome-wide sets of SNP-markers that are generally weighted equally in their contributions. Proposed methods to handle dependence between SNPs include, “thinning” the marker set by linkage disequilibrium (LD)-pruning, the use of haplotype-tagging of SNPs, and LD-weighting of the SNP-contributions. For improved estimation, we propose a new conceptual framework for genomic relationship matrix, in which Mahalanobis distance-based LD-correction is used in a linear mixed model estimation of SNP-heritability. The superiority of the presented method is illustrated and compared to mixed-model analyses using a VanRaden genomic relationship matrix, a matrix used by GCTA and a matrix employing LD-weighting (as implemented in the LDAK software) in simulated (using real human, rice and cattle genotypes) and real (maize, rice and mice) datasets. Despite of the computational difficulties, our results suggest that by using the proposed method one can improve the accuracy of SNP-heritability estimates in datasets with high LD. Springer International Publishing 2017-12-14 2018-04 /pmc/articles/PMC5842222/ /pubmed/29238077 http://dx.doi.org/10.1038/s41437-017-0023-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. If you remix, transform, or build upon this article or a part thereof, you must distribute your contributions under the same license as the original. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/.
spellingShingle Article
Mathew, Boby
Léon, Jens
Sillanpää, Mikko J.
A novel linkage-disequilibrium corrected genomic relationship matrix for SNP-heritability estimation and genomic prediction
title A novel linkage-disequilibrium corrected genomic relationship matrix for SNP-heritability estimation and genomic prediction
title_full A novel linkage-disequilibrium corrected genomic relationship matrix for SNP-heritability estimation and genomic prediction
title_fullStr A novel linkage-disequilibrium corrected genomic relationship matrix for SNP-heritability estimation and genomic prediction
title_full_unstemmed A novel linkage-disequilibrium corrected genomic relationship matrix for SNP-heritability estimation and genomic prediction
title_short A novel linkage-disequilibrium corrected genomic relationship matrix for SNP-heritability estimation and genomic prediction
title_sort novel linkage-disequilibrium corrected genomic relationship matrix for snp-heritability estimation and genomic prediction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842222/
https://www.ncbi.nlm.nih.gov/pubmed/29238077
http://dx.doi.org/10.1038/s41437-017-0023-4
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