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Average semivariance directly yields accurate estimates of the genomic variance in complex trait analyses

Many important traits in plants, animals, and microbes are polygenic and challenging to improve through traditional marker-assisted selection. Genomic prediction addresses this by incorporating all genetic data in a mixed model framework. The primary method for predicting breeding values is genomic...

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Autores principales: Feldmann, Mitchell J, Piepho, Hans-Peter, Knapp, Steven J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157152/
https://www.ncbi.nlm.nih.gov/pubmed/35442424
http://dx.doi.org/10.1093/g3journal/jkac080
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author Feldmann, Mitchell J
Piepho, Hans-Peter
Knapp, Steven J
author_facet Feldmann, Mitchell J
Piepho, Hans-Peter
Knapp, Steven J
author_sort Feldmann, Mitchell J
collection PubMed
description Many important traits in plants, animals, and microbes are polygenic and challenging to improve through traditional marker-assisted selection. Genomic prediction addresses this by incorporating all genetic data in a mixed model framework. The primary method for predicting breeding values is genomic best linear unbiased prediction, which uses the realized genomic relationship or kinship matrix (K) to connect genotype to phenotype. Genomic relationship matrices share information among entries to estimate the observed entries’ genetic values and predict unobserved entries’ genetic values. One of the main parameters of such models is genomic variance ([Formula: see text]), or the variance of a trait associated with a genome-wide sample of DNA polymorphisms, and genomic heritability ([Formula: see text]); however, the seminal papers introducing different forms of K often do not discuss their effects on the model estimated variance components despite their importance in genetic research and breeding. Here, we discuss the effect of several standard methods for calculating the genomic relationship matrix on estimates of [Formula: see text] and [Formula: see text]. With current approaches, we found that the genomic variance tends to be either overestimated or underestimated depending on the scaling and centering applied to the marker matrix (Z), the value of the average diagonal element of K, and the assortment of alleles and heterozygosity (H) in the observed population. Using the average semivariance, we propose a new matrix, [Formula: see text] , that directly yields accurate estimates of [Formula: see text] and [Formula: see text] in the observed population and produces best linear unbiased predictors equivalent to routine methods in plants and animals.
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spelling pubmed-91571522022-06-04 Average semivariance directly yields accurate estimates of the genomic variance in complex trait analyses Feldmann, Mitchell J Piepho, Hans-Peter Knapp, Steven J G3 (Bethesda) Investigation Many important traits in plants, animals, and microbes are polygenic and challenging to improve through traditional marker-assisted selection. Genomic prediction addresses this by incorporating all genetic data in a mixed model framework. The primary method for predicting breeding values is genomic best linear unbiased prediction, which uses the realized genomic relationship or kinship matrix (K) to connect genotype to phenotype. Genomic relationship matrices share information among entries to estimate the observed entries’ genetic values and predict unobserved entries’ genetic values. One of the main parameters of such models is genomic variance ([Formula: see text]), or the variance of a trait associated with a genome-wide sample of DNA polymorphisms, and genomic heritability ([Formula: see text]); however, the seminal papers introducing different forms of K often do not discuss their effects on the model estimated variance components despite their importance in genetic research and breeding. Here, we discuss the effect of several standard methods for calculating the genomic relationship matrix on estimates of [Formula: see text] and [Formula: see text]. With current approaches, we found that the genomic variance tends to be either overestimated or underestimated depending on the scaling and centering applied to the marker matrix (Z), the value of the average diagonal element of K, and the assortment of alleles and heterozygosity (H) in the observed population. Using the average semivariance, we propose a new matrix, [Formula: see text] , that directly yields accurate estimates of [Formula: see text] and [Formula: see text] in the observed population and produces best linear unbiased predictors equivalent to routine methods in plants and animals. Oxford University Press 2022-04-20 /pmc/articles/PMC9157152/ /pubmed/35442424 http://dx.doi.org/10.1093/g3journal/jkac080 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
Feldmann, Mitchell J
Piepho, Hans-Peter
Knapp, Steven J
Average semivariance directly yields accurate estimates of the genomic variance in complex trait analyses
title Average semivariance directly yields accurate estimates of the genomic variance in complex trait analyses
title_full Average semivariance directly yields accurate estimates of the genomic variance in complex trait analyses
title_fullStr Average semivariance directly yields accurate estimates of the genomic variance in complex trait analyses
title_full_unstemmed Average semivariance directly yields accurate estimates of the genomic variance in complex trait analyses
title_short Average semivariance directly yields accurate estimates of the genomic variance in complex trait analyses
title_sort average semivariance directly yields accurate estimates of the genomic variance in complex trait analyses
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157152/
https://www.ncbi.nlm.nih.gov/pubmed/35442424
http://dx.doi.org/10.1093/g3journal/jkac080
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