Evidence map›Paper›PMID 39152403›Full record

ArticleGenetics, selection, evolution : GSE2024

A computationally feasible multi-trait single-step genomic prediction model with trait-specific marker weights.

Ismo Strandén, Janez Jenko

Abstract read
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Article in Genetics, selection, evolution : GSE, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from 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

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5 · Who and what money

Authors and funding

2 authors.

Ismo StrandénNatural Resources Institute Finland (Luke), Jokioinen, Finland. ismo.stranden@luke.fi.ORCID http://orcid.org/0000-0003-0161-2618
Janez JenkoGeno SA, Storhamargata 44, 2317, Hamar, Norway.

Funding

Norwegian Research Council 309611
6 · The paper itself

Abstract

backgroundRegions of genome-wide marker data may have differing influences on the evaluated traits. This can be reflected in the genomic models by assigning different weights to the markers, which can enhance the accuracy of genomic prediction. However, the standard multi-trait single-step genomic evaluation model can be computationally infeasible when the traits are allowed to have different marker weights.

resultsIn this study, we developed and implemented a multi-trait single-step single nucleotide polymorphism best linear unbiased prediction (SNPBLUP) model for large genomic data evaluations that allows for the use of precomputed trait-specific marker weights. The modifications to the standard single-step SNPBLUP model were minor and did not significantly increase the preprocessing workload. The model was tested using simulated data and marker weights precomputed using BayesA. Based on the results, memory requirements and computing time per iteration slightly increased compared to the standard single-step model without weights. Moreover, convergence of the model was slower when using marker weights, which resulted in longer total computing time. The use of marker weights, however, improved prediction accuracy.

conclusionsWe investigated a single-step SNPBLUP model that can be used to accommodate trait-specific marker weights. The marker-weighted single-step model improved prediction accuracy. The approach can be used for large genomic data evaluations using precomputed marker weights.

Indexed as

GenomicsModels, GeneticPolymorphism, Single NucleotideAnimalsComputer SimulationGenetic MarkersPhenotypeQuantitative Trait, HeritableQuantitative Trait LociGenetic Markers

Identifiers

PMID39152403
PMCPMC11328383

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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.