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Benefits of Dominance over Additive Models for the Estimation of Average Effects in the Presence of Dominance

In quantitative genetics, the average effect at a single locus can be estimated by an additive (A) model, or an additive plus dominance (AD) model. In the presence of dominance, the AD-model is expected to be more accurate, because the A-model falsely assumes that residuals are independent and ident...

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Autores principales: Duenk, Pascal, Calus, Mario P. L., Wientjes, Yvonne C. J., Bijma, Piter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633389/
https://www.ncbi.nlm.nih.gov/pubmed/28842396
http://dx.doi.org/10.1534/g3.117.300113
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author Duenk, Pascal
Calus, Mario P. L.
Wientjes, Yvonne C. J.
Bijma, Piter
author_facet Duenk, Pascal
Calus, Mario P. L.
Wientjes, Yvonne C. J.
Bijma, Piter
author_sort Duenk, Pascal
collection PubMed
description In quantitative genetics, the average effect at a single locus can be estimated by an additive (A) model, or an additive plus dominance (AD) model. In the presence of dominance, the AD-model is expected to be more accurate, because the A-model falsely assumes that residuals are independent and identically distributed. Our objective was to investigate the accuracy of an estimated average effect ([Formula: see text]) in the presence of dominance, using either a single locus A-model or AD-model. Estimation was based on a finite sample from a large population in Hardy-Weinberg equilibrium (HWE), and the root mean squared error of [Formula: see text] was calculated for several broad-sense heritabilities, sample sizes, and sizes of the dominance effect. Results show that with the A-model, both sampling deviations of genotype frequencies from HWE frequencies and sampling deviations of allele frequencies contributed to the error. With the AD-model, only sampling deviations of allele frequencies contributed to the error, provided that all three genotype classes were sampled. In the presence of dominance, the root mean squared error of [Formula: see text] with the AD-model was always smaller than with the A-model, even when the heritability was less than one. Remarkably, in the absence of dominance, there was no disadvantage of fitting dominance. In conclusion, the AD-model yields more accurate estimates of average effects from a finite sample, because it is more robust against sampling deviations from HWE frequencies than the A-model. Genetic models that include dominance, therefore, yield higher accuracies of estimated average effects than purely additive models when dominance is present.
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spelling pubmed-56333892017-10-18 Benefits of Dominance over Additive Models for the Estimation of Average Effects in the Presence of Dominance Duenk, Pascal Calus, Mario P. L. Wientjes, Yvonne C. J. Bijma, Piter G3 (Bethesda) Investigations In quantitative genetics, the average effect at a single locus can be estimated by an additive (A) model, or an additive plus dominance (AD) model. In the presence of dominance, the AD-model is expected to be more accurate, because the A-model falsely assumes that residuals are independent and identically distributed. Our objective was to investigate the accuracy of an estimated average effect ([Formula: see text]) in the presence of dominance, using either a single locus A-model or AD-model. Estimation was based on a finite sample from a large population in Hardy-Weinberg equilibrium (HWE), and the root mean squared error of [Formula: see text] was calculated for several broad-sense heritabilities, sample sizes, and sizes of the dominance effect. Results show that with the A-model, both sampling deviations of genotype frequencies from HWE frequencies and sampling deviations of allele frequencies contributed to the error. With the AD-model, only sampling deviations of allele frequencies contributed to the error, provided that all three genotype classes were sampled. In the presence of dominance, the root mean squared error of [Formula: see text] with the AD-model was always smaller than with the A-model, even when the heritability was less than one. Remarkably, in the absence of dominance, there was no disadvantage of fitting dominance. In conclusion, the AD-model yields more accurate estimates of average effects from a finite sample, because it is more robust against sampling deviations from HWE frequencies than the A-model. Genetic models that include dominance, therefore, yield higher accuracies of estimated average effects than purely additive models when dominance is present. Genetics Society of America 2017-08-25 /pmc/articles/PMC5633389/ /pubmed/28842396 http://dx.doi.org/10.1534/g3.117.300113 Text en Copyright © 2017 Duenk et al. 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
Duenk, Pascal
Calus, Mario P. L.
Wientjes, Yvonne C. J.
Bijma, Piter
Benefits of Dominance over Additive Models for the Estimation of Average Effects in the Presence of Dominance
title Benefits of Dominance over Additive Models for the Estimation of Average Effects in the Presence of Dominance
title_full Benefits of Dominance over Additive Models for the Estimation of Average Effects in the Presence of Dominance
title_fullStr Benefits of Dominance over Additive Models for the Estimation of Average Effects in the Presence of Dominance
title_full_unstemmed Benefits of Dominance over Additive Models for the Estimation of Average Effects in the Presence of Dominance
title_short Benefits of Dominance over Additive Models for the Estimation of Average Effects in the Presence of Dominance
title_sort benefits of dominance over additive models for the estimation of average effects in the presence of dominance
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633389/
https://www.ncbi.nlm.nih.gov/pubmed/28842396
http://dx.doi.org/10.1534/g3.117.300113
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