Evidence map›Paper›PMID 38459504›Full record

ArticleGenetics, selection, evolution : GSE2024

Confidence intervals for validation statistics with data truncation in genomic prediction.

Matias Bermann, Andres Legarra, Alejandra Alvarez Munera, Ignacy Misztal, Daniela Lourenco

Open access · goldAbstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Matias BermannDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA. mbermann@uga.edu.ORCID http://orcid.org/0000-0002-5374-0710
Andres LegarraCouncil on Dairy Cattle Breeding (CDCB), Bowie, MD, 20716, USA.
Alejandra Alvarez MuneraDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA.
Ignacy MisztalDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA.
Daniela LourencoDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA.
University of Georgia · USDairy Management · US

Funding

National Institute of Food and Agriculture 2020-67015-31030
6 · The paper itself

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.

Indexed as

GenomicsModels, GeneticConfidence IntervalsGenotypeHumansPedigreePhenotypeReproducibility of Results

Identifiers

PMID38459504
PMCPMC11234739
OpenAlexW4392592897

What OpenQuestion holds

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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.