Evidence map›Paper›PMID 26564950›Full record

ArticleG3 (Bethesda, Md.)2015

Genomic Prediction Accounting for Residual Heteroskedasticity.

Zhining Ou, Robert J Tempelman, Juan P Steibel, Catherine W Ernst, Ronald O Bates, Nora M Bello

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Better Multi-Breed Genomic Predictions for Tropical Bull Fertility Using a Breed-Adjusted Genomic Relationship Matrix.Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie · 2026
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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

6 authors.

Zhining OuDepartment of Statistics, Kansas State University, Manhattan, Kansas 66506.
Robert J TempelmanDepartment of Animal Science, Michigan State University, East Lansing, Michigan 48824.
Juan P SteibelDepartment of Animal Science, Michigan State University, East Lansing, Michigan 48824 Department of Fisheries and Wildlife, Michigan State University, East Lansing, Michigan 48824.
Catherine W ErnstDepartment of Animal Science, Michigan State University, East Lansing, Michigan 48824.
Ronald O BatesDepartment of Animal Science, Michigan State University, East Lansing, Michigan 48824.
Nora M BelloDepartment of Statistics, Kansas State University, Manhattan, Kansas 66506 nbello@ksu.edu.ORCID http://orcid.org/0000-0002-3902-1533

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whole-genome prediction (WGP) models that use single-nucleotide polymorphism marker information to predict genetic merit of animals and plants typically assume homogeneous residual variance. However, variability is often heterogeneous across agricultural production systems and may subsequently bias WGP-based inferences. This study extends classical WGP models based on normality, heavy-tailed specifications and variable selection to explicitly account for environmentally-driven residual heteroskedasticity under a hierarchical Bayesian mixed-models framework. WGP models assuming homogeneous or heterogeneous residual variances were fitted to training data generated under simulation scenarios reflecting a gradient of increasing heteroskedasticity. Model fit was based on pseudo-Bayes factors and also on prediction accuracy of genomic breeding values computed on a validation data subset one generation removed from the simulated training dataset. Homogeneous vs. heterogeneous residual variance WGP models were also fitted to two quantitative traits, namely 45-min postmortem carcass temperature and loin muscle pH, recorded in a swine resource population dataset prescreened for high and mild residual heteroskedasticity, respectively. Fit of competing WGP models was compared using pseudo-Bayes factors. Predictive ability, defined as the correlation between predicted and observed phenotypes in validation sets of a five-fold cross-validation was also computed. Heteroskedastic error WGP models showed improved model fit and enhanced prediction accuracy compared to homoskedastic error WGP models although the magnitude of the improvement was small (less than two percentage points net gain in prediction accuracy). Nevertheless, accounting for residual heteroskedasticity did improve accuracy of selection, especially on individuals of extreme genetic merit.

Indexed as

Genetic Association StudiesGenomeGenomicsModels, GeneticPhenotypeAlgorithmsAnimalsComputer SimulationQuantitative Trait, HeritableSwinegenomic breeding valuesgenPredheteroskedastic errorshierarchical Bayesian modelshared data resourcewhole-genome prediction

Identifiers

PMID26564950
PMCPMC4704708

What OpenQuestion holds

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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.