ArticleGenetics, selection, evolution : GSE2017
Application of a Bayesian dominance model improves power in quantitative trait genome-wide association analysis.
Article in Genetics, selection, evolution : GSE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Genomic Selection for Milk Yield and Milk Composition Traits in Dairy Goats Using Machine Learning and Prior-Information Models.Animals : an open access journal from MDPI · 2026Article
- Heterogeneity of variance and genetic parameters for milk production in cattle, using Bayesian inference.PloS one · 2023Article
- Estimating dominance genetic variances for growth traits in American Angus males using genomic models.Journal of animal science · 2020Article
- An approximate Bayesian significance test for genomic evaluations.Biometrical journal. Biometrische Zeitschrift · 2018Article
- Article
- Non-additive Effects in Genomic Selection.Frontiers in genetics · 2018Review
- Benefits of Dominance over Additive Models for the Estimation of Average Effects in the Presence of Dominance.G3 (Bethesda, Md.) · 2017Article
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5 authors.
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Abstract
backgroundMulti-marker methods, which fit all markers simultaneously, were originally tailored for genomic selection purposes, but have proven to be useful also in association analyses, especially the so-called BayesC Bayesian methods. In a recent study, BayesD extended BayesC towards accounting for dominance effects and improved prediction accuracy and persistence in genomic selection. The current study investigated the power and precision of BayesC and BayesD in genome-wide association studies by means of stochastic simulations and applied these methods to a dairy cattle dataset.
methodsThe simulation protocol was designed to mimic the genetic architecture of quantitative traits as realistically as possible. Special emphasis was put on the joint distribution of the additive and dominance effects of causative mutations. Additive marker effects were estimated by BayesC and additive and dominance effects by BayesD. The dependencies between additive and dominance effects were modelled in BayesD by choosing appropriate priors. A sliding-window approach was used. For each window, the R. Fernando window posterior probability of association was calculated and this was used for inference purpose. The power to map segregating causal effects and the mapping precision were assessed for various marker densities up to full sequence information and various window sizes.
resultsPower to map a QTL increased with higher marker densities and larger window sizes. This held true for both methods. Method BayesD had improved power compared to BayesC. The increase in power was between -2 and 8% for causative genes that explained more than 2.5% of the genetic variance. In addition, inspection of the estimates of genomic window dominance variance allowed for inference about the magnitude of dominance at significant associations, which remains hidden in BayesC analysis. Mapping precision was not substantially improved by BayesD.
conclusionsBayesD improved power, but precision only slightly. Application of BayesD needs large datasets with genotypes and own performance records as phenotypes. Given the current efforts to establish cow reference populations in dairy cattle genomic selection schemes, such datasets are expected to be soon available, which will enable the application of BayesD for association mapping and genomic prediction purposes.
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