Cargando…

Incorporation of causative quantitative trait nucleotides in single-step GBLUP

BACKGROUND: Much effort is put into identifying causative quantitative trait nucleotides (QTN) in animal breeding, empowered by the availability of dense single nucleotide polymorphism (SNP) information. Genomic selection using traditional SNP information is easily implemented for any number of geno...

Descripción completa

Detalles Bibliográficos
Autores principales: Fragomeni, Breno O., Lourenco, Daniela A. L., Masuda, Yukata, Legarra, Andres, Misztal, Ignacy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530494/
https://www.ncbi.nlm.nih.gov/pubmed/28747171
http://dx.doi.org/10.1186/s12711-017-0335-0
_version_ 1783253273644367872
author Fragomeni, Breno O.
Lourenco, Daniela A. L.
Masuda, Yukata
Legarra, Andres
Misztal, Ignacy
author_facet Fragomeni, Breno O.
Lourenco, Daniela A. L.
Masuda, Yukata
Legarra, Andres
Misztal, Ignacy
author_sort Fragomeni, Breno O.
collection PubMed
description BACKGROUND: Much effort is put into identifying causative quantitative trait nucleotides (QTN) in animal breeding, empowered by the availability of dense single nucleotide polymorphism (SNP) information. Genomic selection using traditional SNP information is easily implemented for any number of genotyped individuals using single-step genomic best linear unbiased predictor (ssGBLUP) with the algorithm for proven and young (APY). Our aim was to investigate whether ssGBLUP is useful for genomic prediction when some or all QTN are known. METHODS: Simulations included 180,000 animals across 11 generations. Phenotypes were available for all animals in generations 6 to 10. Genotypes for 60,000 SNPs across 10 chromosomes were available for 29,000 individuals. The genetic variance was fully accounted for by 100 or 1000 biallelic QTN. Raw genomic relationship matrices (GRM) were computed from (a) unweighted SNPs, (b) unweighted SNPs and causative QTN, (c) SNPs and causative QTN weighted with results obtained with genome-wide association studies, (d) unweighted SNPs and causative QTN with simulated weights, (e) only unweighted causative QTN, (f–h) as in (b–d) but using only the top 10% causative QTN, and (i) using only causative QTN with simulated weight. Predictions were computed by pedigree-based BLUP (PBLUP) and ssGBLUP. Raw GRM were blended with 1 or 5% of the numerator relationship matrix, or 1% of the identity matrix. Inverses of GRM were obtained directly or with APY. RESULTS: Accuracy of breeding values for 5000 genotyped animals in the last generation with PBLUP was 0.32, and for ssGBLUP it increased to 0.49 with an unweighted GRM, 0.53 after adding unweighted QTN, 0.63 when QTN weights were estimated, and 0.89 when QTN weights were based on true effects known from the simulation. When the GRM was constructed from causative QTN only, accuracy was 0.95 and 0.99 with blending at 5 and 1%, respectively. Accuracies simulating 1000 QTN were generally lower, with a similar trend. Accuracies using the APY inverse were equal or higher than those with a regular inverse. CONCLUSIONS: Single-step GBLUP can account for causative QTN via a weighted GRM. Accuracy gains are maximum when variances of causative QTN are known and blending is at 1%.
format Online
Article
Text
id pubmed-5530494
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-55304942017-08-02 Incorporation of causative quantitative trait nucleotides in single-step GBLUP Fragomeni, Breno O. Lourenco, Daniela A. L. Masuda, Yukata Legarra, Andres Misztal, Ignacy Genet Sel Evol Research Article BACKGROUND: Much effort is put into identifying causative quantitative trait nucleotides (QTN) in animal breeding, empowered by the availability of dense single nucleotide polymorphism (SNP) information. Genomic selection using traditional SNP information is easily implemented for any number of genotyped individuals using single-step genomic best linear unbiased predictor (ssGBLUP) with the algorithm for proven and young (APY). Our aim was to investigate whether ssGBLUP is useful for genomic prediction when some or all QTN are known. METHODS: Simulations included 180,000 animals across 11 generations. Phenotypes were available for all animals in generations 6 to 10. Genotypes for 60,000 SNPs across 10 chromosomes were available for 29,000 individuals. The genetic variance was fully accounted for by 100 or 1000 biallelic QTN. Raw genomic relationship matrices (GRM) were computed from (a) unweighted SNPs, (b) unweighted SNPs and causative QTN, (c) SNPs and causative QTN weighted with results obtained with genome-wide association studies, (d) unweighted SNPs and causative QTN with simulated weights, (e) only unweighted causative QTN, (f–h) as in (b–d) but using only the top 10% causative QTN, and (i) using only causative QTN with simulated weight. Predictions were computed by pedigree-based BLUP (PBLUP) and ssGBLUP. Raw GRM were blended with 1 or 5% of the numerator relationship matrix, or 1% of the identity matrix. Inverses of GRM were obtained directly or with APY. RESULTS: Accuracy of breeding values for 5000 genotyped animals in the last generation with PBLUP was 0.32, and for ssGBLUP it increased to 0.49 with an unweighted GRM, 0.53 after adding unweighted QTN, 0.63 when QTN weights were estimated, and 0.89 when QTN weights were based on true effects known from the simulation. When the GRM was constructed from causative QTN only, accuracy was 0.95 and 0.99 with blending at 5 and 1%, respectively. Accuracies simulating 1000 QTN were generally lower, with a similar trend. Accuracies using the APY inverse were equal or higher than those with a regular inverse. CONCLUSIONS: Single-step GBLUP can account for causative QTN via a weighted GRM. Accuracy gains are maximum when variances of causative QTN are known and blending is at 1%. BioMed Central 2017-07-26 /pmc/articles/PMC5530494/ /pubmed/28747171 http://dx.doi.org/10.1186/s12711-017-0335-0 Text en © The Author(s) 2017 Open AccessThis article is 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 you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Fragomeni, Breno O.
Lourenco, Daniela A. L.
Masuda, Yukata
Legarra, Andres
Misztal, Ignacy
Incorporation of causative quantitative trait nucleotides in single-step GBLUP
title Incorporation of causative quantitative trait nucleotides in single-step GBLUP
title_full Incorporation of causative quantitative trait nucleotides in single-step GBLUP
title_fullStr Incorporation of causative quantitative trait nucleotides in single-step GBLUP
title_full_unstemmed Incorporation of causative quantitative trait nucleotides in single-step GBLUP
title_short Incorporation of causative quantitative trait nucleotides in single-step GBLUP
title_sort incorporation of causative quantitative trait nucleotides in single-step gblup
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530494/
https://www.ncbi.nlm.nih.gov/pubmed/28747171
http://dx.doi.org/10.1186/s12711-017-0335-0
work_keys_str_mv AT fragomenibrenoo incorporationofcausativequantitativetraitnucleotidesinsinglestepgblup
AT lourencodanielaal incorporationofcausativequantitativetraitnucleotidesinsinglestepgblup
AT masudayukata incorporationofcausativequantitativetraitnucleotidesinsinglestepgblup
AT legarraandres incorporationofcausativequantitativetraitnucleotidesinsinglestepgblup
AT misztalignacy incorporationofcausativequantitativetraitnucleotidesinsinglestepgblup