Evidence map›Paper›PMID 24498162›Full record

ArticlePloS one2014

Mixed model methods for genomic prediction and variance component estimation of additive and dominance effects using SNP markers.

Yang Da, Chunkao Wang, Shengwen Wang, Guo Hu

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Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

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52citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

52 citing papers in PubMed.

  1. Impact of scale parameter for marker variance prior in some Bayesian whole-genome regression methods.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yang DaDepartment of Animal Science, University of Minnesota, Saint Paul, Minnesota, United States of America.
Chunkao WangDepartment of Animal Science, University of Minnesota, Saint Paul, Minnesota, United States of America.
Shengwen WangDepartment of Animal Science, University of Minnesota, Saint Paul, Minnesota, United States of America.
Guo HuDepartment of Animal Science, University of Minnesota, Saint Paul, Minnesota, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We established a genomic model of quantitative trait with genomic additive and dominance relationships that parallels the traditional quantitative genetics model, which partitions a genotypic value as breeding value plus dominance deviation and calculates additive and dominance relationships using pedigree information. Based on this genomic model, two sets of computationally complementary but mathematically identical mixed model methods were developed for genomic best linear unbiased prediction (GBLUP) and genomic restricted maximum likelihood estimation (GREML) of additive and dominance effects using SNP markers. These two sets are referred to as the CE and QM sets, where the CE set was designed for large numbers of markers and the QM set was designed for large numbers of individuals. GBLUP and associated accuracy formulations for individuals in training and validation data sets were derived for breeding values, dominance deviations and genotypic values. Simulation study showed that GREML and GBLUP generally were able to capture small additive and dominance effects that each accounted for 0.00005-0.0003 of the phenotypic variance and GREML was able to differentiate true additive and dominance heritability levels. GBLUP of the total genetic value as the summation of additive and dominance effects had higher prediction accuracy than either additive or dominance GBLUP, causal variants had the highest accuracy of GREML and GBLUP, and predicted accuracies were in agreement with observed accuracies. Genomic additive and dominance relationship matrices using SNP markers were consistent with theoretical expectations. The GREML and GBLUP methods can be an effective tool for assessing the type and magnitude of genetic effects affecting a phenotype and for predicting the total genetic value at the whole genome level.

Indexed as

Genetic MarkersGenome, HumanGenomicsGenotypeHumansLikelihood FunctionsModels, GeneticPedigreePhenotypePolymorphism, Single NucleotideQuantitative Trait, HeritableGenetic Markers

Identifiers

PMID24498162
PMCPMC3907568

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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.