Evidence map›Paper›PMID 40119282›Full record

ArticleGenetics, selection, evolution : GSE2025

Multitrait genome-wide association best linear unbiased prediction of genetic values.

Theo Meuwissen, Vinzent Boerner

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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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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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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Theo MeuwissenFaculty of Life Sciences, Norwegian University of Life Sciences, 1432, Ås, Norway. theo.meuwissen@nmbu.no.ORCID http://orcid.org/0000-0003-3019-4283
Vinzent BoernerGHPC Consulting and Service PTY, LTD, Armidale, Australia.

Funding

Norges Forskningsråd 309611
6 · The paper itself

Abstract

backgroundThe GWABLUP (Genome-Wide Association based Best Linear Unbiased Prediction) approach used GWA analysis results to differentially weigh the SNPs in genomic prediction, and was found to improve the reliabilities of genomic predictions. However, the proposed multitrait GWABLUP method assumed that the SNP weights were the same across the traits. Here we extended and validated the multitrait GWABLUP method towards using trait specific SNP weights.

resultsIn a 3-trait dairy data set, multitrait GWAS estimates of SNP effects and their standard errors were translated into trait specific likelihood ratios for the SNPs having trait effects, and posterior probabilities using the GWABLUP approach. This produced trait specific prior (co)variance matrices for each SNP, which were applied in a SNP-BLUP model for genomic predictions, implemented in the APEX linear model suite. In a validation population, the trait specific SNP weights resulted in more reliable predictions for all three traits. Especially, for somatic cell count, which was hardly related to the other traits, the use of the same weights across all traits was harming genomic predictions. The use of trait specific SNP weights overcame this problem.

conclusionsIn multitrait GWABLUP analyses of ~ 30,000 reference population cows, trait specific SNP weights resulted in up to 13% more reliable genomic predictions than unweighted SNP-BLUP, and improved genomic predictions for all three studied traits.

Indexed as

Genome-Wide Association StudyModels, GeneticAnimalsCattleFemaleGenomicsLinear ModelsPhenotypePolymorphism, Single NucleotideQuantitative Trait Loci

Identifiers

PMID40119282
PMCPMC11927129

What Socratic holds

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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 Socratic graph.