Evidence map›Paper›PMID 40186488›Full record

ArticleGenetics2025

Estimation of heritabilities and genetic correlations by time slices using predictivity in large genomic models.

Ignacy Misztal, Gopal Gowane

Abstract read
In one paragraph

Article in Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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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.

Ignacy MisztalAnimal and Dairy Science, University of Georgia, Athens, GA 30602, USA.ORCID 0000-0002-0382-1897
Gopal GowaneOn leave from Animal Genetics and Breding Division, ICAR-National Dairy Research Institute, Karnal 132001, India.ORCID 0000-0001-6535-7818

Funding

Agriculture and Food Research Initiative Competitive 2024-67015-42255US Department of Agriculture's National Institute of Food and Agriculture
6 · The paper itself

Abstract

Under genomic selection, genetic parameters may change rapidly from generation to generation. Unless genetic parameters used for a selection index are current, the expected genetic gain may be unrealistic, possibly with a decline for antagonistic traits. Existing methods for parameter estimation are computationally unfeasible with large genomic data. We present formulas for estimating heritabilities and genetic correlations applicable for large models with any number of genotyped individuals. Heritabilities are calculated by combining 2 formulas for genomic accuracies: one that relies on predictivity and another that depends on the number of independent chromosome segments. Genetic correlations are calculated from predictivities across traits. We simulated data including 2 traits for 240,000 genotyped and phenotyped animals in 6 generations, namely, production trait with an initial heritability of 0.4 and a fitness trait with a fixed heritability set at 0.1 in each generation. Only the first trait (production) was selected, whereas the second trait (fitness) was constructed so that its genetic correlation with the first trait declined by about 0.1 per generation. Calculations were for 3-generation windows, with the first 2 generations treated as a reference population. Compared with realized values, the estimated heritabilities were within 0.02. Genetic correlations were within 0.15 with predictivity of production phenotype by prediction for fitness and within 0.05 with predictivity of the fitness phenotype by prediction for production. The proposed formulas enable the estimation of heritabilities and genetic correlations by time slices for models in which predictivities can be calculated and genetic evaluation is feasible.

Indexed as

GenomicsModels, GeneticQuantitative Trait, HeritableAnimalsComputer SimulationGenetic FitnessGenotypePhenotypeSelection, Geneticcorrelated responsegenetic correlationgenetic parametersgenomic predictiongenomic selectionheritabilitylarge dataparameter estimationpredictability

Identifiers

PMID40186488
PMCPMC12135196

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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.