Evidence map›Paper›PMID 31267147›Full record

ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2019

Training set determination for genomic selection.

Jen-Hsiang Ou, Chen-Tuo Liao

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Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Multi-trait ridge regression BLUP withFrontiers in plant science · 2025
    Article
  8. Article
  9. Constructing training sets for genomic selection to identify superior genotypes in candidate populations.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Sample size determination for training set optimization in genomic prediction.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2023
    Article
  15. A comparison of methods for training population optimization in genomic selection.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2023
    Article
  16. Article
  17. Selection of parental lines for plant breedingFrontiers in plant science · 2022
    Article
  18. Genomic Prediction: Progress and Perspectives for Rice Improvement.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  19. Article
  20. Genomic prediction and training set optimization in a structured Mediterranean oat population.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2021
    Article
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

2 authors.

Jen-Hsiang OuDepartment of Agronomy, National Taiwan University, Taipei, Taiwan.
Chen-Tuo LiaoDepartment of Agronomy, National Taiwan University, Taipei, Taiwan. ctliao@ntu.edu.tw.ORCID http://orcid.org/0000-0001-9777-3701

Funding

Ministry of Science and Technology, Taiwan MOST 106-2118-M-002-002-MY2
6 · The paper itself

Abstract

key messageA new optimality criterion is proposed to determine a training set for genomic selection, which is derived from Pearson's correlation between GEBVs and phenotypic values of a test set. R functions are provided to generate the optimal training set. For a specified test set, we develop a highly efficient algorithm to determine an optimal subset from a large candidate set in which the individuals have been genotyped but not phenotyped yet. The chosen subset serves as a training set to be phenotyped, and then a genomic selection (GS) model is built based on its phenotype and genotype data. In this study, we consider the additive effects whole-genome regression model and adopt ridge regression estimation for marker effects in the GS model. The resulting GS model is then employed to predict genomic estimated breeding values (GEBVs) for the individuals of the test set, which have been genotyped only. We propose a new optimality criterion to determine the required training set, which is derived directly from Pearson's correlation between GEBVs and phenotypic values of the test set. Pearson's correlation is the standard measure for prediction accuracy of a GS model. Our proposed methods can be applied to data with the varying degree of population structure. All the R functions for implementing our training set determination algorithms are available from the R package TSDFGS. The algorithms are illustrated with two datasets which have strong (rice genome dataset) and mild (wheat genome dataset) population structures. Our methods are shown to be advantageous over existing ones, mainly because they fully use the genomic relationship between the test set and the training set by taking into account both the variance and bias for predicting GEBVs.

Indexed as

AlgorithmsQuantitative Trait LociSelection, GeneticGenomicsGenotypeModels, GeneticOryzaPhenotypePlant BreedingTriticum

Identifiers

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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.