Evidence map›Paper›PMID 35842585›Full record

ArticleGenetics, selection, evolution : GSE2022

On the equivalence between marker effect models and breeding value models and direct genomic values with the Algorithm for Proven and Young.

Matias Bermann, Daniela Lourenco, Natalia S Forneris, Andres Legarra, Ignacy Misztal

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Article in Genetics, selection, evolution : GSE, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

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11citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Matias BermannDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA. mbermann@uga.edu.ORCID http://orcid.org/0000-0002-5374-0710
Daniela LourencoDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA.
Natalia S FornerisFacultad de Agronomía, Universidad de Buenos Aires, C1417DSQ, Buenos Aires, Argentina.
Andres LegarraINRA, UMR1388 GenPhySE, 31326, Castanet-Tolosan, France.
Ignacy MisztalDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA.

Funding

Horizon 2020 772787National Institute of Food and Agriculture 2020-67015-31030
6 · The paper itself

Abstract

backgroundSingle-step genomic predictions obtained from a breeding value model require calculating the inverse of the genomic relationship matrix [Formula: see text]. The Algorithm for Proven and Young (APY) creates a sparse representation of [Formula: see text] with a low computational cost. APY consists of selecting a group of core animals and expressing the breeding values of the remaining animals as a linear combination of those from the core animals plus an error term. The objectives of this study were to: (1) extend APY to marker effects models; (2) derive equations for marker effect estimates when APY is used for breeding value models, and (3) show the implication of selecting a specific group of core animals in terms of a marker effects model.

resultsWe derived a family of marker effects models called APY-SNP-BLUP. It differs from the classic marker effects model in that the row space of the genotype matrix is reduced and an error term is fitted for non-core animals. We derived formulas for marker effect estimates that take this error term in account. The prediction error variance (PEV) of the marker effect estimates depends on the PEV for core animals but not directly on the PEV of the non-core animals. We extended the APY-SNP-BLUP to include a residual polygenic effect and accommodate non-genotyped animals. We show that selecting a specific group of core animals is equivalent to select a subspace of the row space of the genotype matrix. As the number of core animals increases, subspaces corresponding to different sets of core animals tend to overlap, showing that random selection of core animals is algebraically justified.

conclusionsThe APY-(ss)GBLUP models can be expressed in terms of marker effect models. When the number of core animals is equal to the rank of the genotype matrix, APY-SNP-BLUP is identical to the classic marker effects model. If the number of core animals is less than the rank of the genotype matrix, genotypes for non-core animals are imputed as a linear combination of the genotypes of the core animals. For estimating SNP effects, only relationships and estimated breeding values for core animals are needed.

Indexed as

GenomeModels, GeneticAlgorithmsAnimalsGenomicsGenotypePedigreePhenotype

Identifiers

PMID35842585
PMCPMC9288049

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.