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Estimating genetic variance contributed by a quantitative trait locus: A random model approach

Detecting quantitative trait loci (QTL) and estimating QTL variances (represented by the squared QTL effects) are two main goals of QTL mapping and genome-wide association studies (GWAS). However, there are issues associated with estimated QTL variances and such issues have not attracted much attent...

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Detalles Bibliográficos
Autores principales: Wang, Shibo, Xie, Fangjie, Xu, Shizhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8942241/
https://www.ncbi.nlm.nih.gov/pubmed/35275920
http://dx.doi.org/10.1371/journal.pcbi.1009923
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author Wang, Shibo
Xie, Fangjie
Xu, Shizhong
author_facet Wang, Shibo
Xie, Fangjie
Xu, Shizhong
author_sort Wang, Shibo
collection PubMed
description Detecting quantitative trait loci (QTL) and estimating QTL variances (represented by the squared QTL effects) are two main goals of QTL mapping and genome-wide association studies (GWAS). However, there are issues associated with estimated QTL variances and such issues have not attracted much attention from the QTL mapping community. Estimated QTL variances are usually biased upwards due to estimation being associated with significance tests. The phenomenon is called the Beavis effect. However, estimated variances of QTL without significance tests can also be biased upwards, which cannot be explained by the Beavis effect; rather, this bias is due to the fact that QTL variances are often estimated as the squares of the estimated QTL effects. The parameters are the QTL effects and the estimated QTL variances are obtained by squaring the estimated QTL effects. This square transformation failed to incorporate the errors of estimated QTL effects into the transformation. The consequence is biases in estimated QTL variances. To correct the biases, we can either reformulate the QTL model by treating the QTL effect as random and directly estimate the QTL variance (as a variance component) or adjust the bias by taking into account the error of the estimated QTL effect. A moment method of estimation has been proposed to correct the bias. The method has been validated via Monte Carlo simulation studies. The method has been applied to QTL mapping for the 10-week-body-weight trait from an F(2) mouse population.
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spelling pubmed-89422412022-03-24 Estimating genetic variance contributed by a quantitative trait locus: A random model approach Wang, Shibo Xie, Fangjie Xu, Shizhong PLoS Comput Biol Research Article Detecting quantitative trait loci (QTL) and estimating QTL variances (represented by the squared QTL effects) are two main goals of QTL mapping and genome-wide association studies (GWAS). However, there are issues associated with estimated QTL variances and such issues have not attracted much attention from the QTL mapping community. Estimated QTL variances are usually biased upwards due to estimation being associated with significance tests. The phenomenon is called the Beavis effect. However, estimated variances of QTL without significance tests can also be biased upwards, which cannot be explained by the Beavis effect; rather, this bias is due to the fact that QTL variances are often estimated as the squares of the estimated QTL effects. The parameters are the QTL effects and the estimated QTL variances are obtained by squaring the estimated QTL effects. This square transformation failed to incorporate the errors of estimated QTL effects into the transformation. The consequence is biases in estimated QTL variances. To correct the biases, we can either reformulate the QTL model by treating the QTL effect as random and directly estimate the QTL variance (as a variance component) or adjust the bias by taking into account the error of the estimated QTL effect. A moment method of estimation has been proposed to correct the bias. The method has been validated via Monte Carlo simulation studies. The method has been applied to QTL mapping for the 10-week-body-weight trait from an F(2) mouse population. Public Library of Science 2022-03-11 /pmc/articles/PMC8942241/ /pubmed/35275920 http://dx.doi.org/10.1371/journal.pcbi.1009923 Text en © 2022 Wang et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wang, Shibo
Xie, Fangjie
Xu, Shizhong
Estimating genetic variance contributed by a quantitative trait locus: A random model approach
title Estimating genetic variance contributed by a quantitative trait locus: A random model approach
title_full Estimating genetic variance contributed by a quantitative trait locus: A random model approach
title_fullStr Estimating genetic variance contributed by a quantitative trait locus: A random model approach
title_full_unstemmed Estimating genetic variance contributed by a quantitative trait locus: A random model approach
title_short Estimating genetic variance contributed by a quantitative trait locus: A random model approach
title_sort estimating genetic variance contributed by a quantitative trait locus: a random model approach
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8942241/
https://www.ncbi.nlm.nih.gov/pubmed/35275920
http://dx.doi.org/10.1371/journal.pcbi.1009923
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