ArticleGenetics, selection, evolution : GSE2024
Confidence intervals for validation statistics with data truncation in genomic prediction.
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 7 papers.
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Who cites it
7 citing papers in PubMed, 9 citations in OpenAlex.
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- The multi-target protective effects of quercetin in cerebrovascular diseases: a dietary strategy for endothelial repair and neuroprotection.Frontiers in nutrition · 2026Review
- Semi-parametric validation of genomic predictions and polygenic risk scores with the Blupf90 software suite.G3 (Bethesda, Md.) · 2025Article
- Genotyping strategies for single-step genomic predictions in a simulated sheep population under different scenarios of pedigree error types.Frontiers in genetics · 2025Article
- Comment on: "Hematological Toxicity of PARP Inhibitors in Metastatic Prostate Cancer Patients with Mutations of BRCA or HRR Genes: A Systematic Review and Safety Meta‑analysis".Targeted oncology · 2024Article
- Combining large broiler populations into a single genomic evaluation: dealing with genetic divergence.Journal of animal science · 2024Article
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
Abstract
backgroundValidation by data truncation is a common practice in genetic evaluations because of the interest in predicting the genetic merit of a set of young selection candidates. Two of the most used validation methods in genetic evaluations use a single data partition: predictivity or predictive ability (correlation between pre-adjusted phenotypes and estimated breeding values (EBV) divided by the square root of the heritability) and the linear regression (LR) method (comparison of "early" and "late" EBV). Both methods compare predictions with the whole dataset and a partial dataset that is obtained by removing the information related to a set of validation individuals. EBV obtained with the partial dataset are compared against adjusted phenotypes for the predictivity or EBV obtained with the whole dataset in the LR method. Confidence intervals for predictivity and the LR method can be obtained by replicating the validation for different samples (or folds), or bootstrapping. Analytical confidence intervals would be beneficial to avoid running several validations and to test the quality of the bootstrap intervals. However, analytical confidence intervals are unavailable for predictivity and the LR method.
resultsWe derived standard errors and Wald confidence intervals for the predictivity and statistics included in the LR method (bias, dispersion, ratio of accuracies, and reliability). The confidence intervals for the bias, dispersion, and reliability depend on the relationships and prediction error variances and covariances across the individuals in the validation set. We developed approximations for large datasets that only need the reliabilities of the individuals in the validation set. The confidence intervals for the ratio of accuracies and predictivity were obtained through the Fisher transformation. We show the adequacy of both the analytical and approximated analytical confidence intervals and compare them versus bootstrap confidence intervals using two simulated examples. The analytical confidence intervals were closer to the simulated ones for both examples. Bootstrap confidence intervals tend to be narrower than the simulated ones. The approximated analytical confidence intervals were similar to those obtained by bootstrapping.
conclusionsEstimating the sampling variation of predictivity and the statistics in the LR method without replication or bootstrap is possible for any dataset with the formulas presented in this study.
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