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Realized Genome Sharing in Heritability Estimation Using Random Effects Models

For heritability estimation using a two-component random effects model, we provided formulas for the limiting distribution of the maximum likelihood estimate. These formulas are applicable even when the wrong measure of kinship is used to capture additive genetic correlation. When the model is corre...

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Autores principales: Wang, Bowen, Thompson, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505141/
https://www.ncbi.nlm.nih.gov/pubmed/30902892
http://dx.doi.org/10.1534/g3.119.0005
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author Wang, Bowen
Thompson, Elizabeth
author_facet Wang, Bowen
Thompson, Elizabeth
author_sort Wang, Bowen
collection PubMed
description For heritability estimation using a two-component random effects model, we provided formulas for the limiting distribution of the maximum likelihood estimate. These formulas are applicable even when the wrong measure of kinship is used to capture additive genetic correlation. When the model is correctly specified, we showed that the asymptotic sampling variance of heritability estimate is determined by both the study design and the extent of variation in the kinship measure that constitutes the additive genetic correlation matrix. When the correlation matrix is mis-specified, the extent of asymptotic bias depends additionally on how the fitted correlation matrix differs from the truth. In particular, we showed in a simulation study that estimating heritability using a population-based design and the classic GRM as the fitted correlation matrix can potentially contribute to the ”missing heritability” problem.
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spelling pubmed-65051412019-05-21 Realized Genome Sharing in Heritability Estimation Using Random Effects Models Wang, Bowen Thompson, Elizabeth G3 (Bethesda) Investigations For heritability estimation using a two-component random effects model, we provided formulas for the limiting distribution of the maximum likelihood estimate. These formulas are applicable even when the wrong measure of kinship is used to capture additive genetic correlation. When the model is correctly specified, we showed that the asymptotic sampling variance of heritability estimate is determined by both the study design and the extent of variation in the kinship measure that constitutes the additive genetic correlation matrix. When the correlation matrix is mis-specified, the extent of asymptotic bias depends additionally on how the fitted correlation matrix differs from the truth. In particular, we showed in a simulation study that estimating heritability using a population-based design and the classic GRM as the fitted correlation matrix can potentially contribute to the ”missing heritability” problem. Genetics Society of America 2019-03-22 /pmc/articles/PMC6505141/ /pubmed/30902892 http://dx.doi.org/10.1534/g3.119.0005 Text en Copyright © 2019 Wang, Thompson http://creativecommons.org/licenses/by/4.0/ This is an open-access article 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 the original work is properly cited.
spellingShingle Investigations
Wang, Bowen
Thompson, Elizabeth
Realized Genome Sharing in Heritability Estimation Using Random Effects Models
title Realized Genome Sharing in Heritability Estimation Using Random Effects Models
title_full Realized Genome Sharing in Heritability Estimation Using Random Effects Models
title_fullStr Realized Genome Sharing in Heritability Estimation Using Random Effects Models
title_full_unstemmed Realized Genome Sharing in Heritability Estimation Using Random Effects Models
title_short Realized Genome Sharing in Heritability Estimation Using Random Effects Models
title_sort realized genome sharing in heritability estimation using random effects models
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505141/
https://www.ncbi.nlm.nih.gov/pubmed/30902892
http://dx.doi.org/10.1534/g3.119.0005
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