Evidence map›Paper›PMID 42663655›Full record

ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2026

Unveiling the interactions between design optimization, modeling strategies, and spatial analysis in genomic selection.

Javier Fernández-González, Jordi Comadran Trabal, Bertrand Haquin, Alix Allard, Eliette Combes, Karine Bernard, Julio Isidro Y Sánchez

Abstract read
In one paragraph

Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 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. Article
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

7 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, 28223, Pozuelo de Alarcón, Madrid, Spain. javier.fgonzalez@upm.es.
Jordi Comadran TrabalSyngenta, Saint-Sauveur, France.
Bertrand HaquinSyngenta, Saint-Sauveur, France.
Alix AllardSyngenta, Saint-Sauveur, France.
Eliette CombesSyngenta, Saint-Sauveur, France.
Karine BernardSyngenta, Saint-Sauveur, France.
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, 28223, Pozuelo de Alarcón, Madrid, Spain. julio.isidro@csic.es.

Funding

Agencia Estatal de Investigación Severo Ochoa Program for Centers of Excellence in R&DMCIN/AEI/10.13039/501100011033, and "ERDF A way of making Europe,CEX2020-000999-S PID2021-123718OB-I00Ministerio de Ciencia, Innovación y Universidades FPU22/02543
6 · The paper itself

Abstract

key messagePartially-replicated designs are more efficient than fully-replicated ones. They can be further enhanced through optimization and present positive synergy with fully-efficient models and 2D P-splines. In plant breeding, traditional field trials rely on balanced designs with high replication to ensure robust breeding value predictions. However, genomic technologies leveraging genomic relationship matrices have reduced the need for extensive replication, favoring partially-replicated (p-rep) designs. These designs, while effective, pose statistical challenges due to low replication and imbalance. To address these, we conducted simulations using datasets from maize, sunflower, and oat, evaluating interactions between experimental designs and modeling strategies across varying field sizes. Classical and p-rep designs, generated via randomization or optimization, were compared, using a novel, faster implementation of the CDmean optimization criterion developed to overcome computational limits. Modeling strategies included single-stage models, unweighted and fully efficient two-stage analysis, and spatial analysis with blocking structures or high-resolution 2D P-splines. Our findings showed p-rep designs consistently outperformed classical designs in predicting unobserved lines, achieving 1-25% higher accuracies depending on the scenario. Within observed training sets, p-rep designs exhibited slightly lower accuracy than classical designs, but it is compensated with increased selection intensity. Design optimization enhanced accuracy by  1% over randomized p-rep designs, while 2D P-splines improved accuracy by 1-2% when paired with single-stage or fully efficient models.

Indexed as

Genome, PlantGenomicsModels, GeneticPlant BreedingSelection, GeneticAvenaComputer SimulationHelianthusSpatial AnalysisZea mays

Identifiers

PMID42663655
PMCPMC13524979

What OpenQuestion holds

Textmetadata
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.