Evidence map›Paper›PMID 28693539›Full record

ArticleBMC genomics2017

Genomic prediction in contrast to a genome-wide association study in explaining heritable variation of complex growth traits in breeding populations of Eucalyptus.

Bárbara S F Müller, Leandro G Neves, Janeo E de Almeida Filho, Márcio F R Resende, Patricio R Muñoz, Paulo E T Dos Santos, Estefano Paludzyszyn Filho, Matias Kirst, Dario Grattapaglia

Abstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

34 citing papers in PubMed.

  1. Article
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  4. Population structure limits the use of genomic data for predicting phenotypes and managing genetic resources in forest trees.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  7. Genomic prediction of resistance toEvolutionary applications · 2024
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  11. Review
  12. Genomic selection in tropical perennial crops and plantation trees: a review.Molecular breeding : new strategies in plant improvement · 2022
    Review
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  17. Article
  18. Review
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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

9 authors.

Bárbara S F MüllerCell Biology Department, Molecular Biology Program, Biological Sciences Institute, University of Brasília, Campus Darcy Ribeiro, Brasília, DF, 70910-900, Brazil.
Leandro G NevesRAPiD Genomics LLC, Gainesville, FL, 32601, USA.
Janeo E de Almeida FilhoForest Genomics Laboratory, School of Forest Resources and Conservation, University of Florida, Gainesville, FL, 32611, USA.
Márcio F R ResendeRAPiD Genomics LLC, Gainesville, FL, 32601, USA.
Patricio R MuñozAgronomy Department, University of Florida, Gainesville, FL, 32611, USA.
Paulo E T Dos SantosEMBRAPA Forestry, Estrada da Ribeira, Km 111, Colombo, PR, 83411-000, Brazil.
Estefano Paludzyszyn FilhoEMBRAPA Forestry, Estrada da Ribeira, Km 111, Colombo, PR, 83411-000, Brazil.
Matias KirstForest Genomics Laboratory, School of Forest Resources and Conservation, University of Florida, Gainesville, FL, 32611, USA.
Dario GrattapagliaCell Biology Department, Molecular Biology Program, Biological Sciences Institute, University of Brasília, Campus Darcy Ribeiro, Brasília, DF, 70910-900, Brazil. dario.grattapaglia@embrapa.br.ORCID 0000-0002-0050-970X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe advent of high-throughput genotyping technologies coupled to genomic prediction methods established a new paradigm to integrate genomics and breeding. We carried out whole-genome prediction and contrasted it to a genome-wide association study (GWAS) for growth traits in breeding populations of Eucalyptus benthamii (n =505) and Eucalyptus pellita (n =732). Both species are of increasing commercial interest for the development of germplasm adapted to environmental stresses.

resultsPredictive ability reached 0.16 in E. benthamii and 0.44 in E. pellita for diameter growth. Predictive abilities using either Genomic BLUP or different Bayesian methods were similar, suggesting that growth adequately fits the infinitesimal model. Genomic prediction models using ~5000-10,000 SNPs provided predictive abilities equivalent to using all 13,787 and 19,506 SNPs genotyped in the E. benthamii and E. pellita populations, respectively. No difference was detected in predictive ability when different sets of SNPs were utilized, based on position (equidistantly genome-wide, inside genes, linkage disequilibrium pruned or on single chromosomes), as long as the total number of SNPs used was above ~5000. Predictive abilities obtained by removing relatedness between training and validation sets fell near zero for E. benthamii and were halved for E. pellita. These results corroborate the current view that relatedness is the main driver of genomic prediction, although some short-range historical linkage disequilibrium (LD) was likely captured for E. pellita. A GWAS identified only one significant association for volume growth in E. pellita, illustrating the fact that while genome-wide regression is able to account for large proportions of the heritability, very little or none of it is captured into significant associations using GWAS in breeding populations of the size evaluated in this study.

conclusionsThis study provides further experimental data supporting positive prospects of using genome-wide data to capture large proportions of trait heritability and predict growth traits in trees with accuracies equal or better than those attainable by phenotypic selection. Additionally, our results document the superiority of the whole-genome regression approach in accounting for large proportions of the heritability of complex traits such as growth in contrast to the limited value of the local GWAS approach toward breeding applications in forest trees.

Indexed as

BreedingGenome-Wide Association StudyGenomicsBayes TheoremEucalyptusGenome, PlantLinkage DisequilibriumPhenotypePolymorphism, Single NucleotideE. pellitaEucalyptus benthamiiGenomic selectionGWASRelatednessSNP genotypingTree breeding

Identifiers

PMID28693539
PMCPMC5504793

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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.