Evidence map›Paper›PMID 42919126›Full record

ArticleGenetics, selection, evolution : GSE2026

A deregression-based approach to integrate multitrait information into a single pooled phenotype for genetic evaluation.

Alice Markey, Nicolas Gengler

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Article in Genetics, selection, evolution : GSE, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited 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

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Alice Markey *TERRA Teaching and Research Center, Gembloux Agro-Bio Tech, University of Liège, Gembloux, 5030, Belgium. alice.markey@uliege.be.ORCID http://orcid.org/0000-0003-0154-6016
Nicolas Gengler *TERRA Teaching and Research Center, Gembloux Agro-Bio Tech, University of Liège, Gembloux, 5030, Belgium.ORCID http://orcid.org/0000-0002-5981-5509

Funding

Direction Générale Opérationnelle Agriculture, Ressources Naturelles et Environnement du Service Public de Wallonie D31-1396Direction Générale Opérationnelle Agriculture, Ressources Naturelles et Environnement du Service Public de Wallonie D65-1430Direction Générale Opérationnelle Agriculture, Ressources Naturelles et Environnement du Service Public de Wallonie Walloon Pig Genomic Evaluation SystemFonds De La Recherche Scientifique - FNRS T.0095.19
6 · The paper itself

Abstract

backgroundGenetic evaluation of complex traits is often challenged by heterogeneous, incomplete or costly phenotyping. Many biological processes require multiple traits to be characterized. Moreover, combining several traits becomes difficult when the configuration of available traits is complex (e.g., increasing number, complex missing patterns), leading to more demanding computations. To overcome these limitations, a deregression-based pooling method was developed to pre-process multitrait information into a single pseudo-phenotype of the target trait (i.e., a pooled phenotype). This method was assessed in a terminal crossbreeding situation in pigs.

resultsThe behavior of estimated breeding values and the accuracy of reliabilities systems were studied on different datasets (i.e., different data availability scenarios - a real and 3 simulated). Three modeling steps were used: (1) a multitrait model generating input for deregressions, (2) an adjusted scalar deregression, combining information into a pooled phenotype using (3) a single trait model applied to this pooled phenotype to assess how these results match the multitrait predictions from step (1). In all data structure scenarios, unadjusted deregression underestimates breeding values and distorts reliabilities. In contrast, applying expansion and reliability-alignment factors as adjustments restored the distributions and scale of estimated breeding values, yielding a near-perfect agreement with the multitrait model. Across all simulated scenarios, including the one with the complete absence of the target trait, the adjusted deregression process achieved the highest correlations between true and estimated breeding values.

conclusionsThe deregression-based process provides an effective and flexible approach for combining heterogeneous multitrait information into a unique pooled phenotype in a single trait setting, while maintaining genetic scale and reliability of the target trait in a multiple trait setting. Unlike classical deregression, the adjusted deregression process prevents overshrinking, maintains accuracy and reproduces the behavior of a multitrait evaluation. This pre-processing would be a practical solution for integrating complex or partially recorded traits into routine genetic evaluation pipelines. This method is applicable even if the main target trait is limited or missing, provided that moderately to highly correlated traits are available. The strategy could be extended to other situations as long as any double-counting can be avoided.

Indexed as

BreedingModels, GeneticPhenotypeAnimalsComputer SimulationQuantitative Trait, HeritableQuantitative Trait LociSwine

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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.