Evidence map›Paper›PMID 41840952›Full record

ArticleThe plant genome2026

Randomization across breeding cohorts improves the accuracy of conventional and genomic selection.

Arlyn Ackerman, Jessica Rutkoski

Abstract read
In one paragraph

Article in The plant genome, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

2 authors.

Arlyn AckermanBreeding Insight, Cornell University, Ithaca, New York, USA.
Jessica RutkoskiDepartment of Crop Sciences, University of Illinois at Urbana-Champaign, Champaign, Illinois, USA.ORCID https://orcid.org/0000-0001-8435-4049

Funding

Department of Crop Sciences at the University of Illinois Urbana-ChampaignSiemer Milling CompanyUSDA, National Institute of Food and Agriculture 2022-68013-36439USDA, National Institute of Food and Agriculture 2023-67013-39612USDA, National Institute of Food and Agriculture ILLU-802-974U.S. Wheat and Barley Scab Initiative 59-0206-0-143U.S. Wheat and Barley Scab Initiative 59-0206-2-165
6 · The paper itself

Abstract

Breeding programs conventionally evaluate cohorts in separate trials; however, environmental differences across testing areas can be confounded with genetic differences between cohorts, potentially reducing the accuracy of breeding value estimation. We test whether the conventional approach of restricting randomization of cohorts to within trials reduces genomic and conventional selection accuracy when compared to the complete randomization of all cohorts across a trial, using in silico simulation with marker data from University of Illinois winter wheat breeding lines. We evaluated selection accuracy for conventional best linear unbiased prediction (BLUP), genomic BLUP (GBLUP), and genomic-enabled sparse testing across a comprehensive simulation space spanning narrow-sense heritabilities of 0.2-0.8, genetic correlations between testing areas from 0.2 to 1.0, and three replication levels. Difference-in-differences (DiD) analysis established causal inference by comparing design performance as conditions deteriorated from an optimal baseline where both designs performed equivalently. Complete randomization improved BLUP accuracy by 11.7%, reaching 15.7% under low replication and low genetic correlation between areas. Genomic data largely eliminated this design effect, with GBLUP showing no significant DiD interaction effect. However, genomic-enabled sparse testing revealed a significant DiD effect and an improvement in selection accuracy of 1.5% that increased to a 5.5% advantage under challenging conditions. While heritability had the strongest main effect on selection accuracy, genetic correlation between areas showed the largest interaction with randomization scheme, with design performance diverging significantly only as this parameter decreased. Programs with genomic data and balanced phenotypic data can use either restricted or complete randomization, but those with other circumstances can benefit from complete randomization.

Indexed as

Genome, PlantGenomicsPlant BreedingSelection, GeneticTriticumComputer SimulationModels, Genetic

Identifiers

PMID41840952
PMCPMC12993266

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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.