Evidence map›Paper›PMID 35114933›Full record

ArticleGenetics, selection, evolution : GSE2022

Computing strategies for multi-population genomic evaluation.

Andrés Legarra, David González-Diéguez, Zulma G Vitezica

Open access · goldAbstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2022. 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
0.4field-weighted citation impact, top 35% of its field
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, 2 citations in OpenAlex.

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

3 authors at 2 institutions in 2 countries.

Andrés LegarraINRAE, INP, UMR 1388 GenPhySE, 31326, Castanet-Tolosan, France. andres.legarra@inrae.fr.ORCID http://orcid.org/0000-0001-8893-7620
David González-DiéguezINRAE, INP, UMR 1388 GenPhySE, 31326, Castanet-Tolosan, France.ORCID http://orcid.org/0000-0002-8637-1835
Zulma G VitezicaINRAE, INP, UMR 1388 GenPhySE, 31326, Castanet-Tolosan, France.ORCID http://orcid.org/0000-0002-3162-7258
Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FRCentro Internacional de Mejoramiento de Maíz Y Trigo · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultiple breed evaluation using genomic prediction includes the use of data from multiple populations, or from parental breeds and crosses, and is expected to lead to better genomic predictions. Increased complexity comes from the need to fit non-additive effects such as dominance and/or genotype-by-environment interactions. In these models, marker effects (and breeding values) are modelled as correlated between breeds, which leads to multiple trait formulations that are based either on markers [single nucleotide polymorphism best linear unbiased prediction (SNP-BLUP)] or on individuals [genomic(G)BLUP)]. As an alternative, we propose the use of generalized least squares (GLS) followed by backsolving of marker effects using selection index (SI) theory.

resultsAll investigated options have advantages and inconveniences. The SNP-BLUP yields marker effects directly, which are useful for indirect prediction and for planned matings, but is very large in number of equations and is structured in dense and sparse blocks that do not allow for simple solving. GBLUP uses a multiple trait formulation and is very general, but results in many equations that are not used, which increase memory needs, and is also structured in dense and sparse blocks. An alternative formulation of GBLUP is more compact but requires tailored programming. The alternative of solving by GLS + SI is the least consuming, both in number of operations and in memory, and it uses only single dense blocks. However, it requires dedicated programming. Computational complexity problems are exacerbated when more than additive effects are fitted, e.g. dominance effects or genotype x environment interactions.

conclusionsAs multi-breed predictions become more frequent and non-additive effects are more often included, standard equations for genomic prediction based on Henderson's mixed model equations become less practical and may need to be replaced by more efficient (although less general) approaches such as the GLS + SI approach proposed here.

Indexed as

Genetics, PopulationGenomeMetagenomicsModels, GeneticBreedingGenomicsGenotypePolymorphism, Single Nucleotide

Identifiers

PMID35114933
PMCPMC8815165
OpenAlexW4210339175

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.