Evidence map›Paper›PMID 41553380›Full record

ArticleGenetics2026

MateR: a novel genomic mating framework.

Javier Fernández-González, Seifelden M Metwally, Julio Isidro Y Sánchez

Abstract read
In one paragraph

Article in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

3 authors.

Javier Fernández-GonzálezCentro de Biotecnologia y Genómica de Plantas (CBGP, UPM-INIA), Universidad Politécnica de Madrid (UPM) - Instituto Nacional de Investigación y Tecnologia Agraria y Alimentaria (INIA), Campus de Montegancedo-UPM, Pozuelo de Alarcón, Madrid 28223, Spain.
Seifelden M MetwallyCentro de Biotecnologia y Genómica de Plantas (CBGP, UPM-INIA), Universidad Politécnica de Madrid (UPM) - Instituto Nacional de Investigación y Tecnologia Agraria y Alimentaria (INIA), Campus de Montegancedo-UPM, Pozuelo de Alarcón, Madrid 28223, Spain.ORCID 0000-0001-8501-2913
Julio Isidro Y SánchezCentro de Biotecnologia y Genómica de Plantas (CBGP, UPM-INIA), Universidad Politécnica de Madrid (UPM) - Instituto Nacional de Investigación y Tecnologia Agraria y Alimentaria (INIA), Campus de Montegancedo-UPM, Pozuelo de Alarcón, Madrid 28223, Spain.ORCID 0000-0002-9044-3221

Funding

MCIN/AEI/10.13039/501100011033 PLEC2023-010225Ministerio Ciencia, Innovación y UniversidadesMinisterio de Ciencia, Innovación y Universidades PID2021-123718OB-I00
6 · The paper itself

Abstract

Genomic mating uses genome-wide information to design crosses that maximize genetic gain while managing diversity. Expected gain is often predicted through the usefulness criterion, which depends on family means and variances. However, existing equations mix incompatible parameterizations when considering dominance effects. Furthermore, diversity control is often tuned with metrics that lack a direct link to the loss of additive variation and long-term gain. We derived equations that compute family mean and within-family variance consistently under breeding and genotypic parameterizations by computing locus-specific values using genotypic frequencies and propagating them to the entire genome through linkage disequilibrium covariances. We also developed a diversity metric that estimates the proportion of additive standard deviation lost and integrated both advances into the MateR software. We evaluated performance in simulated diploid and autotetraploid crop populations across multiple breeding schemes and against existing tools. The new equations predicted family means and variances with near-perfect accuracy when true QTL effects were known. With estimated marker effects, correlations were roughly 0.55-0.90 for family mean and about 0.25 for within-family standard deviation. The diversity metric matched the expected loss of additive standard deviation under random sampling and tracked loss of genic variance under selection. This framework unifies prediction of cross usefulness under dominance and supplies an interpretable diversity control directly tied to long-term gain. Implemented in MateR, it applies to diploids and autopolyploids and accommodates common breeding program constraints, including hybrid schemes and testers.

Indexed as

GenomicsModels, GeneticPlant BreedingSoftwareCrosses, GeneticGenetic VariationGenome, PlantGenotypeLinkage DisequilibriumQuantitative Trait LociSelection, Geneticgenomic matinggenomic predictioninbreeding controloptimal contribution selectionoptimal mate allocationusefulness criterion

Identifiers

PMID41553380
PMCPMC13050210

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Registered trials

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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.