Evidence map›Paper›PMID 28957330›Full record

ArticlePloS one2017

Application of single step genomic BLUP under different uncertain paternity scenarios using simulated data.

Rafael Lara Tonussi, Rafael Medeiros de Oliveira Silva, Ana Fabrícia Braga Magalhães, Rafael Espigolan, Elisa Peripolli, Bianca Ferreira Olivieri, Fabieli Loise Braga Feitosa, Marcos Vinicíus Antunes Lemos, Mariana Piatto Berton, Hermenegildo Lucas Justino Chiaia and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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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

17 authors at 4 institutions in 3 countries.

Rafael Lara TonussiDepartment of Animal Science, School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.
Rafael Medeiros de Oliveira SilvaDepartment of Animal Science, School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.
Ana Fabrícia Braga MagalhãesDepartment of Animal Science, School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.
Rafael EspigolanDepartment of Animal Science, School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.
Elisa PeripolliDepartment of Animal Science, School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.
Bianca Ferreira OlivieriDepartment of Animal Science, School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.
Fabieli Loise Braga FeitosaDepartment of Animal Science, School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.
Marcos Vinicíus Antunes LemosDepartment of Animal Science, School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.
Mariana Piatto BertonDepartment of Animal Science, School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.
Hermenegildo Lucas Justino ChiaiaDepartment of Animal Science, School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.
Angelica Simone Cravo PereiraDepartment of Nutrition and Animal Production, Faculty of Animal Science and Food Engineering, Pirassununga, Brazil.
Raysildo Barbosa LôboNational Association of Breeders and Researchers (ANCP), Ribeirão Preto, Brazil.
Luiz Antônio Framartino BezerraDepartment of Genetic, Medical School of Ribeirão Preto, Ribeirão Preto, Brazil.
Cláudio de Ulhoa MagnaboscoBrazilian Agricultural Research Corporation (EMBRAPA), Distrito Federal, Brazil.
Daniela Andressa Lino LourençoDepartment of Animal and Dairy Science, University of Georgia, Athens, Georgia, United States of America.
Ignácio AguilarDepartment of Animal Breeding, National Institute of Agricultural Research, Las Brujas, Uruguay.
Fernando BaldiDepartment of Animal Science, School of Agricultural and Veterinarian Sciences, Jaboticabal, São Paulo, Brazil.
Brazilian Agricultural Research Corporation · BRClinics Hospital of Ribeirão Preto · BRInstituto Nacional de Investigación Agropecuaria · UYUniversity of Georgia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of this study was to investigate the application of BLUP and single step genomic BLUP (ssGBLUP) models in different scenarios of paternity uncertainty with different strategies of scaling the G matrix to match the A22 matrix, using simulated data for beef cattle. Genotypes, pedigree, and phenotypes for age at first calving (AFC) and weight at 550 days (W550) were simulated using heritabilities based on real data (0.12 for AFC and 0.34 for W550). Paternity uncertainty scenarios using 0, 25, 50, 75, and 100% of multiple sires (MS) were studied. The simulated genome had a total length of 2,333 cM, containing 735,293 biallelic markers and 7,000 QTLs randomly distributed over the 29 BTA. It was assumed that QTLs explained 100% of the genetic variance. For QTL, the amount of alleles per loci randomly ranged from two to four. The BLUP model that considers phenotypic and pedigree data, and the ssGBLUP model that combines phenotypic, pedigree and genomic information were used for genetic evaluations. Four ways of scaling the mean of the genomic matrix (G) to match to the mean of the pedigree relationship matrix among genotyped animals (A22) were tested. Accuracy, bias, and inflation were investigated for five groups of animals: ALL = all animals; BULL = only bulls; GEN = genotyped animals; FEM = females; and YOUNG = young males. With the BLUP model, the accuracies of genetic evaluations decreased for both traits as the proportion of unknown sires in the population increased. The EBV accuracy reduction was higher for GEN and YOUNG groups. By analyzing the scenarios for YOUNG (from 0 to 100% of MS), the decrease was 87.8 and 86% for AFC and W550, respectively. When applying the ssGBLUP model, the accuracies of genetic evaluation also decreased as the MS in the pedigree for both traits increased. However, the accuracy reduction was less than those observed for BLUP model. Using the same comparison (scenario 0 to 100% of MS), the accuracies reductions were 38 and 44.6% for AFC and W550, respectively. There were no differences between the strategies for scaling the G matrix for ALL, BULL, and FEM groups under the different scenarios with missing pedigree. These results pointed out that the uninformative part of the A22 matrix and genotyped animals with paternity uncertainty did not influence the scaling of G matrix. On the basis of the results, it is important to have a G matrix in the same scale of the A22 matrix, especially for the evaluation of young animals in situations with missing pedigree information. In these situations, the ssGBLUP model is an appropriate alternative to obtain a more reliable and less biased estimate of breeding values, especially for young animals with few or no phenotypic records. For accurate and unbiased genomic predictions with ssGBLUP, it is necessary to assure that the G matrix is compatible with the A22 matrix, even in situations with paternity uncertainty.

Indexed as

Computer SimulationUncertaintyAgingAnimalsCattleFemaleGenomicsInheritance PatternsMaleModels, GeneticPedigree

Identifiers

PMID28957330
PMCPMC5619718
OpenAlexW2760790468

What OpenQuestion holds

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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.