Evidence map›Paper›PMID 28049412›Full record

ArticleBMC bioinformatics2017

Genomic prediction with epistasis models: on the marker-coding-dependent performance of the extended GBLUP and properties of the categorical epistasis model (CE).

Johannes W R Martini, Ning Gao, Diercles F Cardoso, Valentin Wimmer, Malena Erbe, Rodolfo J C Cantet, Henner Simianer

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Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

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30citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

30 citing papers in PubMed.

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  9. Incorporating Omics Data in Genomic Prediction.Methods in molecular biology (Clifton, N.J.) · 2022
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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Johannes W R MartiniDepartment of Animal Sciences, Georg-August University, Albrecht Thaer-Weg 3, Göttingen, Germany. jmartin2@gwdg.de.
Ning GaoDepartment of Animal Sciences, Georg-August University, Albrecht Thaer-Weg 3, Göttingen, Germany.
Diercles F CardosoDepartment of Animal Sciences, Georg-August University, Albrecht Thaer-Weg 3, Göttingen, Germany.
Valentin WimmerKWS SAAT SE, Einbeck, Germany.
Malena ErbeDepartment of Animal Sciences, Georg-August University, Albrecht Thaer-Weg 3, Göttingen, Germany.
Rodolfo J C CantetDepartment of Animal Production, University of Buenos Aires, INPA-CONICET, Buenos Aires, Argentina.
Henner SimianerDepartment of Animal Sciences, Georg-August University, Albrecht Thaer-Weg 3, Göttingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEpistasis marker effect models incorporating products of marker values as predictor variables in a linear regression approach (extended GBLUP, EGBLUP) have been assessed as potentially beneficial for genomic prediction, but their performance depends on marker coding. Although this fact has been recognized in literature, the nature of the problem has not been thoroughly investigated so far.

resultsWe illustrate how the choice of marker coding implicitly specifies the model of how effects of certain allele combinations at different loci contribute to the phenotype, and investigate coding-dependent properties of EGBLUP. Moreover, we discuss an alternative categorical epistasis model (CE) eliminating undesired properties of EGBLUP and show that the CE model can improve predictive ability. Finally, we demonstrate that the coding-dependent performance of EGBLUP offers the possibility to incorporate prior experimental information into the prediction method by adapting the coding to already available phenotypic records on other traits.

conclusionBased on our results, for EGBLUP, a symmetric coding {-1,1} or {-1,0,1} should be preferred, whereas a standardization using allele frequencies should be avoided. Moreover, CE can be a valuable alternative since it does not possess the undesired theoretical properties of EGBLUP. However, which model performs best will depend on characteristics of the data and available prior information. Data from previous experiments can for instance be incorporated into the marker coding of EGBLUP.

Indexed as

Epistasis, GeneticModels, GeneticAllelesAnimalsMicePolymorphism, Single NucleotideQuantitative Trait LociTriticumEpistasis modelGenomic predictionInteraction

Identifiers

PMID28049412
PMCPMC5209948

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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.