Evidence map›Paper›PMID 30858235›Full record

ArticleG3 (Bethesda, Md.)2019

New Deep Learning Genomic-Based Prediction Model for Multiple Traits with Binary, Ordinal, and Continuous Phenotypes.

Osval A Montesinos-López, Javier Martín-Vallejo, José Crossa, Daniel Gianola, Carlos M Hernández-Suárez, Abelardo Montesinos-López, Philomin Juliana, Ravi Singh

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Bayesian neural networks for genomic prediction: uncertainty quantification and SNP interpretation with SHAP and GWAS.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Deep learning for genomic selection of aquatic animals.Marine life science & technology · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review
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

8 authors.

Osval A Montesinos-LópezFacultad de Telemática.
Javier Martín-VallejoDepartamento de Estadística, Universidad de Salamanca, c/Espejo 2, Salamanca, 37007, España.
José CrossaInternational Maize and Wheat Improvement Center (CIMMYT), Apdo. Postal 6-641, 06600, Ciudad de México, México j.crossa@cgiar.org aml_uach2004@hotmail.com.ORCID 0000-0001-9429-5855
Daniel GianolaDepartments of Animal Sciences, Dairy Science, and Biostatistics and Medical Informatics, University of Wisconsin-Madison, Wisconsin 53706.
Carlos M Hernández-SuárezFacultad de Ciencias, Universidad de Colima, Colima, 28040, México.
Abelardo Montesinos-LópezDepartamento de Matemáticas, Centro Universitario de Ciencias Exactas e Ingenierías (CUCEI), Universidad de Guadalajara, 44430, Jalisco, México j.crossa@cgiar.org aml_uach2004@hotmail.com.
Philomin JulianaInternational Maize and Wheat Improvement Center (CIMMYT), Apdo. Postal 6-641, 06600, Ciudad de México, México.
Ravi SinghInternational Maize and Wheat Improvement Center (CIMMYT), Apdo. Postal 6-641, 06600, Ciudad de México, México.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple-trait experiments with mixed phenotypes (binary, ordinal and continuous) are not rare in animal and plant breeding programs. However, there is a lack of statistical models that can exploit the correlation between traits with mixed phenotypes in order to improve prediction accuracy in the context of genomic selection (GS). For this reason, when breeders have mixed phenotypes, they usually analyze them using univariate models, and thus are not able to exploit the correlation between traits, which many times helps improve prediction accuracy. In this paper we propose applying deep learning for analyzing multiple traits with mixed phenotype data in terms of prediction accuracy. The prediction performance of multiple-trait deep learning with mixed phenotypes (MTDLMP) models was compared to the performance of univariate deep learning (UDL) models. Both models were evaluated using predictors with and without the genotype × environment (G×E) interaction term (I and WI, respectively). The metric used for evaluating prediction accuracy was Pearson's correlation for continuous traits and the percentage of cases correctly classified (PCCC) for binary and ordinal traits. We found that a modest gain in prediction accuracy was obtained only in the continuous trait under the MTDLMP model compared to the UDL model, whereas for the other traits (1 binary and 2 ordinal) we did not find any difference between the two models. In both models we observed that the prediction performance was better for WI than for I. The MTDLMP model is a good alternative for performing simultaneous predictions of mixed phenotypes (binary, ordinal and continuous) in the context of GS.

Indexed as

Deep LearningGenetic Association StudiesGenomeGenomicsModels, GeneticPhenotypeQuantitative Trait, HeritableAlgorithmsGenome, PlantGenotypePlant BreedingReproducibility of ResultsSelection, Geneticdeep learningGenomic Predictiongenomic selectionGenPredmixed phenotypes (binary ordinal and continuous)multiple-traitplant breedingShared Data Resources

Identifiers

PMID30858235
PMCPMC6505163

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.