Evidence map›Paper›PMID 42311761›Full record

ArticleFrontiers in genetics2026

Derivation of prediction error variance for non-genotyped individuals in genomic selection.

Vinícius Silva Junqueira, Marcos Jun-Iti Yokoo, Fernando Flores Cardoso

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Article in Frontiers in genetics, 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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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Vinícius Silva JunqueiraBayer R&D, Bayer Crop Science, Uberlândia, Brazil.
Marcos Jun-Iti YokooEmbrapa Southeastern Livestock, São Carlos, Brazil.
Fernando Flores CardosoEmbrapa South Livestock, Bagé, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic selection has transformed plant and animal breeding by enabling accurate prediction of genetic merit using DNA markers; however, comprehensive genotyping of all selection candidates remains economically prohibitive for most breeding programs. While breeding programs must decide which subset of individuals to genotype within budget constraints, current approaches rely primarily on experience-based decisions rather than quantitative frameworks. We present explicit mathematical derivations for prediction error variance (PEV) in non-genotyped individuals under mixed model equations, providing a theoretical foundation for evaluating genotyping strategies prospectively. The approach derives PEV expressions for non-genotyped selection candidates under different relationship matrix structures, including pedigree-based, genomic, and hybrid single-step methodologies that combine both information sources. The derivations accommodate complex breeding program structures with historical training populations containing both genotypes and phenotypes alongside contemporary selection candidates with only pedigree information. Using Schur complement methods applied to partitioned mixed model equations, the framework enables calculation of prediction uncertainty without requiring actual phenotypic data from selection candidates. The expressions simplify under different information scenarios, from cases with complete phenotypic data to situations where only relationship information is available. The method was validated through simulations across six scenarios with populations ranging from 180 to 15,500 individuals, confirming numerical equivalence with direct matrix inversion while demonstrating computational and memory advantages that increase with population size. Although genomic relationship matrix operations dominate the complexity, matrix decomposition techniques, including Cholesky factorization and APY methodology, can improve efficiency. The mathematical framework provides quantitative tools for transitioning from experience-based to mathematically-informed genotyping decisions, with applications extending to any field requiring prospective quantification of prediction uncertainty under resource constraints.

Indexed as

budget constrainedmatrix decompositionmixed model equationsprediction uncertaintyschur complement

Identifiers

PMID42311761
PMCPMC13271674

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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.