Evidence map›Paper›PMID 37189059›Full record

ArticleGenetics, selection, evolution : GSE2023

A breed-of-origin of alleles model that includes crossbred data improves predictive ability for crossbred animals in a multi-breed population.

Ana Guillenea, Mogens Sandø Lund, Ross Evans, Vinzent Boerner, Emre Karaman

Open access · goldAbstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
5.6field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Ana GuilleneaCenter for Quantitative Genetics and Genomics, Aarhus University, 8000, Aarhus C, Denmark. ana.guillenea@qgg.au.dk.ORCID http://orcid.org/0000-0002-5008-1043
Mogens Sandø LundCenter for Quantitative Genetics and Genomics, Aarhus University, 8000, Aarhus C, Denmark.
Ross EvansICBF, Link Road, Carrigrohane, Ballincollig, Co. Cork, P31 D452, Ireland.
Vinzent BoernerCenter for Quantitative Genetics and Genomics, Aarhus University, 8000, Aarhus C, Denmark.
Emre KaramanCenter for Quantitative Genetics and Genomics, Aarhus University, 8000, Aarhus C, Denmark.
Aarhus University · DK

Funding

Agencia Nacional de Investigación e Innovacion, Uruguay POS_EXT_2018_1_154296H2020 European Research Council 727213
6 · The paper itself

Abstract

backgroundRecently, crossbred animals have begun to be used as parents in the next generations of dairy and beef cattle systems, which has increased the interest in predicting the genetic merit of those animals. The primary objective of this study was to investigate three available methods for genomic prediction of crossbred animals. In the first two methods, SNP effects from within-breed evaluations are used by weighting them by the average breed proportions across the genome (BPM method) or by their breed-of-origin (BOM method). The third method differs from the BOM in that it estimates breed-specific SNP effects using purebred and crossbred data, considering the breed-of-origin of alleles (BOA method). For within-breed evaluations, and thus for BPM and BOM, 5948 Charolais, 6771 Limousin and 7552 Others (a combined population of other breeds) were used to estimate SNP effects separately within each breed. For the BOA, the purebreds' data were enhanced with data from ~ 4K, ~ 8K or ~ 18K crossbred animals. For each animal, its predictor of genetic merit (PGM) was estimated by considering the breed-specific SNP effects. Predictive ability and absence of bias were estimated for crossbreds and the Limousin and Charolais animals. Predictive ability was measured as the correlation between PGM and the adjusted phenotype, while the regression of the adjusted phenotype on PGM was estimated as a measure of bias.

resultsWith BPM and BOM, the predictive abilities for crossbreds were 0.468 and 0.472, respectively, and with the BOA method, they ranged from 0.490 to 0.510. The performance of the BOA method improved as the number of crossbred animals in the reference increased and with the use of the correlated approach, in which the correlation of SNP effects across the genome of the different breeds was considered. The slopes of regression for PGM on adjusted phenotypes for crossbreds showed overdispersion of the genetic merits for all methods but this bias tended to be reduced by the use of the BOA method and by increasing the number of crossbred animals.

conclusionsFor the estimation of the genetic merit of crossbred animals, the results from this study suggest that the BOA method that accommodates crossbred data can yield more accurate predictions than the methods that use SNP effects from separate within-breed evaluations.

Indexed as

Models, GeneticPolymorphism, Single NucleotideAllelesAnimalsCattleGenomicsGenotypePhenotype

Identifiers

PMID37189059
PMCPMC10184430
OpenAlexW4376610591

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.