Data from: Across population genomic prediction scenarios in which Bayesian variable selection outperforms GBLUP

Background: The use of information across populations is an attractive approach to increase the accuracy of genomic prediction for numerically small populations. However, accuracies of across population genomic prediction, in which reference and selection individuals are from different populations, are currently disappointing. It has been shown for within population genomic prediction that Bayesian variable selection models outperform GBLUP models when the number of QTL underlying the trait is low. Therefore, our objective was to identify across population genomic prediction scenarios in which Bayesian variable selection models outperform GBLUP in terms of prediction accuracy. In this study, high density genotype information of 1033 Holstein Friesian, 105 Groningen White Headed, and 147 Meuse-Rhine-Yssel cows were used. Phenotypes were simulated using two changing variables: (1) the number of QTL underlying the trait (3000, 300, 30, 3), and (2) the correlation between allele substitution effects of QTL across populations, i.e. the genetic correlation of the simulated trait between the populations (1.0, 0.8, 0.4). Results: The accuracy obtained by the Bayesian variable selection model was depending on the number of QTL underlying the trait, with a higher accuracy when the number of QTL was lower. This trend was more pronounced for across population genomic prediction than for within population genomic prediction. It was shown that Bayesian variable selection models have an advantage over GBLUP when the number of QTL underlying the simulated trait was small. This advantage disappeared when the number of QTL underlying the simulated trait was large. The point where the accuracy of Bayesian variable selection and GBLUP became similar was approximately the point where the number of QTL was equal to the number of independent chromosome segments (M e ) across the populations. Conclusion: Bayesian variable selection models outperform GBLUP when the number of QTL underlying the trait is smaller than M e . Across populations, M e is considerably larger than within populations. So, it is more likely to find a number of QTL underlying a trait smaller than M e across populations than within population. Therefore Bayesian variable selection models can help to improve the accuracy of across population genomic prediction.

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Main Authors: van den Berg, S., Calus, M.P.L., Meuwissen, T.H.E., Wientjes, Y.C.J.
Format: Dataset biblioteca
Published: Wageningen UR
Subjects:Bayesian variable selection, GBLUP, accuracy, across population, genomic prediction, number of independent chromosome segments,
Online Access:https://research.wur.nl/en/datasets/data-from-across-population-genomic-prediction-scenarios-in-which
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spelling dig-wur-nl-wurpubs-5346982024-09-30 van den Berg, S. Calus, M.P.L. Meuwissen, T.H.E. Wientjes, Y.C.J. Dataset Data from: Across population genomic prediction scenarios in which Bayesian variable selection outperforms GBLUP 2015 Background: The use of information across populations is an attractive approach to increase the accuracy of genomic prediction for numerically small populations. However, accuracies of across population genomic prediction, in which reference and selection individuals are from different populations, are currently disappointing. It has been shown for within population genomic prediction that Bayesian variable selection models outperform GBLUP models when the number of QTL underlying the trait is low. Therefore, our objective was to identify across population genomic prediction scenarios in which Bayesian variable selection models outperform GBLUP in terms of prediction accuracy. In this study, high density genotype information of 1033 Holstein Friesian, 105 Groningen White Headed, and 147 Meuse-Rhine-Yssel cows were used. Phenotypes were simulated using two changing variables: (1) the number of QTL underlying the trait (3000, 300, 30, 3), and (2) the correlation between allele substitution effects of QTL across populations, i.e. the genetic correlation of the simulated trait between the populations (1.0, 0.8, 0.4). Results: The accuracy obtained by the Bayesian variable selection model was depending on the number of QTL underlying the trait, with a higher accuracy when the number of QTL was lower. This trend was more pronounced for across population genomic prediction than for within population genomic prediction. It was shown that Bayesian variable selection models have an advantage over GBLUP when the number of QTL underlying the simulated trait was small. This advantage disappeared when the number of QTL underlying the simulated trait was large. The point where the accuracy of Bayesian variable selection and GBLUP became similar was approximately the point where the number of QTL was equal to the number of independent chromosome segments (M e ) across the populations. Conclusion: Bayesian variable selection models outperform GBLUP when the number of QTL underlying the trait is smaller than M e . Across populations, M e is considerably larger than within populations. So, it is more likely to find a number of QTL underlying a trait smaller than M e across populations than within population. Therefore Bayesian variable selection models can help to improve the accuracy of across population genomic prediction. Wageningen UR text/html https://research.wur.nl/en/datasets/data-from-across-population-genomic-prediction-scenarios-in-which 10.5061/dryad.rq80k https://edepot.wur.nl/443398 Bayesian variable selection GBLUP accuracy across population genomic prediction number of independent chromosome segments Wageningen University & Research
institution WUR NL
collection DSpace
country Países bajos
countrycode NL
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access En linea
databasecode dig-wur-nl
tag biblioteca
region Europa del Oeste
libraryname WUR Library Netherlands
topic Bayesian variable selection
GBLUP
accuracy
across population
genomic prediction
number of independent chromosome segments
Bayesian variable selection
GBLUP
accuracy
across population
genomic prediction
number of independent chromosome segments
spellingShingle Bayesian variable selection
GBLUP
accuracy
across population
genomic prediction
number of independent chromosome segments
Bayesian variable selection
GBLUP
accuracy
across population
genomic prediction
number of independent chromosome segments
van den Berg, S.
Calus, M.P.L.
Meuwissen, T.H.E.
Wientjes, Y.C.J.
Data from: Across population genomic prediction scenarios in which Bayesian variable selection outperforms GBLUP
description Background: The use of information across populations is an attractive approach to increase the accuracy of genomic prediction for numerically small populations. However, accuracies of across population genomic prediction, in which reference and selection individuals are from different populations, are currently disappointing. It has been shown for within population genomic prediction that Bayesian variable selection models outperform GBLUP models when the number of QTL underlying the trait is low. Therefore, our objective was to identify across population genomic prediction scenarios in which Bayesian variable selection models outperform GBLUP in terms of prediction accuracy. In this study, high density genotype information of 1033 Holstein Friesian, 105 Groningen White Headed, and 147 Meuse-Rhine-Yssel cows were used. Phenotypes were simulated using two changing variables: (1) the number of QTL underlying the trait (3000, 300, 30, 3), and (2) the correlation between allele substitution effects of QTL across populations, i.e. the genetic correlation of the simulated trait between the populations (1.0, 0.8, 0.4). Results: The accuracy obtained by the Bayesian variable selection model was depending on the number of QTL underlying the trait, with a higher accuracy when the number of QTL was lower. This trend was more pronounced for across population genomic prediction than for within population genomic prediction. It was shown that Bayesian variable selection models have an advantage over GBLUP when the number of QTL underlying the simulated trait was small. This advantage disappeared when the number of QTL underlying the simulated trait was large. The point where the accuracy of Bayesian variable selection and GBLUP became similar was approximately the point where the number of QTL was equal to the number of independent chromosome segments (M e ) across the populations. Conclusion: Bayesian variable selection models outperform GBLUP when the number of QTL underlying the trait is smaller than M e . Across populations, M e is considerably larger than within populations. So, it is more likely to find a number of QTL underlying a trait smaller than M e across populations than within population. Therefore Bayesian variable selection models can help to improve the accuracy of across population genomic prediction.
format Dataset
topic_facet Bayesian variable selection
GBLUP
accuracy
across population
genomic prediction
number of independent chromosome segments
author van den Berg, S.
Calus, M.P.L.
Meuwissen, T.H.E.
Wientjes, Y.C.J.
author_facet van den Berg, S.
Calus, M.P.L.
Meuwissen, T.H.E.
Wientjes, Y.C.J.
author_sort van den Berg, S.
title Data from: Across population genomic prediction scenarios in which Bayesian variable selection outperforms GBLUP
title_short Data from: Across population genomic prediction scenarios in which Bayesian variable selection outperforms GBLUP
title_full Data from: Across population genomic prediction scenarios in which Bayesian variable selection outperforms GBLUP
title_fullStr Data from: Across population genomic prediction scenarios in which Bayesian variable selection outperforms GBLUP
title_full_unstemmed Data from: Across population genomic prediction scenarios in which Bayesian variable selection outperforms GBLUP
title_sort data from: across population genomic prediction scenarios in which bayesian variable selection outperforms gblup
publisher Wageningen UR
url https://research.wur.nl/en/datasets/data-from-across-population-genomic-prediction-scenarios-in-which
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