Evidence map›Paper›PMID 40102234›Full record

ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2025

Maximizing the accuracy of genetic variance estimation and using a novel generalized effective sample size to improve simulations.

Javier Fernández-González, Julio Isidro Y Sánchez

Abstract read
In one paragraph

Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 2025. 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. Unveiling the interactions between design optimization, modeling strategies, and spatial analysis in genomic selection.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2026
    Article
  2. Article
  3. 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

2 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.ORCID http://orcid.org/0000-0002-2109-7783
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. j.isidro@upm.es.

Funding

Agencia Estatal de Investigación PID2021-123718OB-I00European Regional Development Fund CEX2020-000999-SMinisterio de Ciencia, Innovación y Universidades FPU22/02543Ministerio de Ciencia, Innovación y Universidades PID2021-123718OB-I00
6 · The paper itself

Abstract

key messageWe developed an improved variance estimation that incorporates prediction error variance as a correction factor, alongside a novel generalized effective sample size to enhance simulations. This approach enables precise control of variance components, accommodating for more flexible and accurate simulations. Phenotypic variation in field trials results from genetic and environmental factors, and understanding this variation is critical for breeding program simulations. Additive genetic variance, a key component, is often estimated using linear mixed models (LMM), but can be biased due to improper scaling of the genomic relationship matrix. Here, we show that this bias can be minimized by incorporating prediction error variance (PEV) as a correction factor. Our results demonstrate that the PEV-based estimation of additive variance significantly improves accuracy, with root mean square errors orders of magnitude lower than traditional methods. This improved accuracy enables more realistic simulations, and we introduce a novel generalized effective sample size (ESS) to further refine simulations by accounting for sampling variation. Our method outperforms standard simulation approaches, allowing flexibility to include complex interactions such as genotype by environment effects. These findings provide a robust framework for variance estimation and simulation in genetic studies, with broad applicability to breeding programs.

Indexed as

Genetic VariationModels, GeneticPlant BreedingComputer SimulationGenotypePhenotypeSample Size

Identifiers

PMID40102234
PMCPMC11919955

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.