Evidence map›Paper›PMID 41168703›Full record

ArticleGenetics, selection, evolution : GSE2025

Estimation of (co)variance components for very large datasets and complex single-step genomic models.

Matias Bermann, Andres Legarra, Ignacio Aguilar, Alejandra Alvarez-Munera, Ignacy Misztal, Daniela Lourenco

Abstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Matias BermannDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA. mbermann@uga.edu.ORCID http://orcid.org/0000-0002-5374-0710
Andres LegarraDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA.
Ignacio AguilarInstituto Nacional de Investigación Agropecuaria (INIA), 11500, Montevideo, Uruguay.
Alejandra Alvarez-MuneraDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA.
Ignacy MisztalDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA.
Daniela LourencoDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA.

Funding

National Institute of Food and Agriculture 2024-67015-42255
6 · The paper itself

Abstract

backgroundVariance components of linear mixed models should be estimated with all the data and information available for a specific statistical model to avoid bias. Due to computational limitations, the estimation for large datasets or complex models is often carried out by subsetting the data, removing genomic information, or simplifying the statistical model. Monte Carlo REML (MC-REML) is a method developed to lift computational limitations, but so far there was no extension for genomic information under the single-step genomic methods. In this study, we extended MC-REML to include large genomic information.

resultsWe developed a method to estimate variance components named Monte Carlo single-step genomic REML (MC-ss-GREML). The core of the method includes repeatedly simulating breeding values under a ssGBLUP model and solving the mixed model equations to approximate traces involving prediction error variances. The REML optimization strategies include Expectation Maximization and Average Information. We tested the accuracy of MC-ss-GREML with a three-trait growth model in beef cattle with maternal effects, with 14 parameters to estimate. The data set had 100,000 animals in the pedigree, of which about 33,000 had records, and 10,000 were genotyped. There were no differences in estimates between MC-ss-GREML and ss-GREML with the exact calculation of the traces (exact ss-GREML). MC-ss-GREML took 14% of the computing time and used 1% of the memory compared to the exact ss-GREML. We tested the computing performance of MC-ss-GREML by estimating variance components in a birth weight model, with much larger data that included 7 million animals in the pedigree, from which 330,000 were genotyped. The estimation converged in 11 rounds and took 121 h, with a peak memory usage of 53 Gb.

conclusionsThe new method, MC-ss-GREML, can estimate variance components with large datasets including many genotyped individuals, at affordable time and memory costs.

Indexed as

GenomicsModels, GeneticAnimalsBreedingCattleFemaleGenotypeMaleMonte Carlo MethodPedigree

Identifiers

PMID41168703
PMCPMC12577077

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.