Evidence map›Paper›PMID 34807267›Full record

ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2022

Assessment of genomic prediction reliability and optimization of experimental designs in multi-environment trials.

Simon Rio, Deniz Akdemir, Tiago Carvalho, Julio Isidro Y Sánchez

Abstract read
In one paragraph

Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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  6. Portability of genomic predictions trained on sparse factorial designs across two maize silage breeding cycles.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2024
    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

4 authors.

Simon RioCentro de Biotecnología 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.ORCID http://orcid.org/0000-0001-7014-8789
Deniz AkdemirCIBMTR (Center for International Blood and Marrow Transplant Research), National Marrow Donor Program/Be The Match, Minneapolis, MN, USA.
Tiago CarvalhoCentro de Biotecnología 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 Y SánchezCentro de Biotecnología 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. j.isidro@upm.es.

Funding

Beatriz Galindo Program BEAGAL18/00115Horizon 2020 818144Severo Ochoa for Centres of Excellence in R&D SEV-2016-0672
6 · The paper itself

Abstract

key messageNew forms of the coefficient of determination can help to forecast the accuracy of genomic prediction and optimize experimental designs in multi-environment trials with genotype-by-environment interactions. In multi-environment trials, the relative performance of genotypes may vary depending on the environmental conditions, and this phenomenon is commonly referred to as genotype-by-environment interaction (G[Formula: see text]E). With genomic prediction, G[Formula: see text]E can be accounted for by modeling the genetic covariance between trials, even when the overall experimental design is highly unbalanced between trials, thanks to the genomic relationship between genotypes. In this study, we propose new forms of the coefficient of determination (CD, i.e., the expected model-based square correlation between a genetic value and its corresponding prediction) that can be used to forecast the genomic prediction reliability of genotypes, both for their trial-specific performance and their mean performance. As the expected prediction reliability based on these new CD criteria is generally a good approximation of the observed reliability, we demonstrate that they can be used to optimize multi-environment trials in the presence of G[Formula: see text]E. In addition, this reliability may be highly variable between genotypes, especially in unbalanced designs with complex pedigree relationships between genotypes. Therefore, it can be useful for breeders to assess it before selecting genotypes based on their predicted genetic values. Using a wheat population evaluated both for simulated and phenology traits, and two maize populations evaluated for grain yield, we illustrate this approach and confirm the value of our new CD criteria.

Indexed as

Plant BreedingResearch DesignGenomicsGenotypeModels, GeneticPhenotypeReproducibility of Results

Identifiers

PMID34807267
PMCPMC8866390

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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.