Evidence map›Paper›PMID 29061123›Full record

ArticleGenetics, selection, evolution : GSE2017

Genomic evaluation for a three-way crossbreeding system considering breed-of-origin of alleles.

Claudia A Sevillano, Jeremie Vandenplas, John W M Bastiaansen, Rob Bergsma, Mario P L Calus

Erratum issuedOpen access · goldAbstract read
In one paragraph

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. An erratum has been issued. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.5field-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

31 citing papers in PubMed, 81 citations in OpenAlex.

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  11. Genomic evaluation for two-way crossbred performance in cattle.Genetics, selection, evolution : GSE · 2023
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  16. Genomic Prediction Methods Accounting for Nonadditive Genetic Effects.Methods in molecular biology (Clifton, N.J.) · 2022
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  18. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Claudia A SevillanoWageningen University & Research Animal Breeding and Genomics, 6700 AH, Wageningen, The Netherlands. claudia.sevillanodelaguila@wur.nl.
Jeremie VandenplasWageningen University & Research Animal Breeding and Genomics, 6700 AH, Wageningen, The Netherlands.
John W M BastiaansenWageningen University & Research Animal Breeding and Genomics, 6700 AH, Wageningen, The Netherlands.
Rob BergsmaTopigs Norsvin Research Center, 6640 AA, Beuningen, The Netherlands.
Mario P L CalusWageningen University & Research Animal Breeding and Genomics, 6700 AH, Wageningen, The Netherlands.
Wageningen University & Research · NLTopigs Norsvin (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenomic prediction of purebred animals for crossbred performance can be based on a model that estimates effects of single nucleotide polymorphisms (SNPs) in purebreds on crossbred performance. For crossbred performance, SNP effects might be breed-specific due to differences between breeds in allele frequencies and linkage disequilibrium patterns between SNPs and quantitative trait loci. Accurately tracing the breed-of-origin of alleles (BOA) in three-way crosses is possible with a recently developed procedure called BOA. A model that accounts for breed-specific SNP effects (BOA model), has never been tested empirically on a three-way crossbreeding scheme. Therefore, the objectives of this study were to evaluate the estimates of variance components and the predictive accuracy of the BOA model compared to models in which SNP effects for crossbred performance were assumed to be the same across breeds, using either breed-specific allele frequencies ([Formula: see text] model) or allele frequencies averaged across breeds ([Formula: see text] model). In this study, we used data from purebred and three-way crossbred pigs on average daily gain (ADG), back fat thickness (BF), and loin depth (LD).

resultsEstimates of variance components for crossbred performance from the BOA model were mostly similar to estimates from models [Formula: see text] and [Formula: see text]. Heritabilities for crossbred performance ranged from 0.24 to 0.46 between traits. Genetic correlations between purebred and crossbred performance ([Formula: see text]) across breeds ranged from 0.30 to 0.62 for ADG and from 0.53 to 0.74 for BF and LD. For ADG, prediction accuracies of the BOA model were higher than those of the [Formula: see text] and [Formula: see text] models, with significantly higher accuracies only for one maternal breed. For BF and LD, prediction accuracies of models [Formula: see text] and [Formula: see text] were higher than those of the BOA model, with no significant differences. Across all traits, models [Formula: see text] and [Formula: see text] yielded similar predictions.

conclusionsThe BOA model yielded a higher prediction accuracy for ADG in one maternal breed, which had the lowest [Formula: see text] (0.30). Using the BOA model was especially relevant for traits with a low [Formula: see text]. In all other cases, the use of crossbred information in models [Formula: see text] and [Formula: see text], does not jeopardize predictions and these models are more easily implemented than the BOA model.

Indexed as

AllelesHybridization, GeneticModels, GeneticPedigreeSelective BreedingAnimalsPolymorphism, Single NucleotideSwine

Identifiers

PMID29061123
PMCPMC5653471
OpenAlexW2765875302

What OpenQuestion 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 OpenQuestion graph.