Evidence map›Paper›PMID 35442424›Full record

ArticleG3 (Bethesda, Md.)2022

Average semivariance directly yields accurate estimates of the genomic variance in complex trait analyses.

Mitchell J Feldmann, Hans-Peter Piepho, Steven J Knapp

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. bioRxiv : the preprint server for biology · 2026
    Article
  2. 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
    Article
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  4. A major QTL region associated with powdery mildew resistance in leaves and fruits of the reconstructed garden strawberry.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025
    Article
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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

3 authors at 2 institutions in 2 countries.

Mitchell J FeldmannDepartment of Plant Sciences, University of California, Davis, CA 95616, USA.ORCID 0000-0002-7257-3401
Hans-Peter PiephoBiostatistics Unit, Institute of Crop Science, University of Hohenheim, 70593 Stuttgart, Germany.
Steven J KnappDepartment of Plant Sciences, University of California, Davis, CA 95616, USA.ORCID 0000-0001-6498-5409
University of California, Davis · USUniversity of Hohenheim · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many important traits in plants, animals, and microbes are polygenic and challenging to improve through traditional marker-assisted selection. Genomic prediction addresses this by incorporating all genetic data in a mixed model framework. The primary method for predicting breeding values is genomic best linear unbiased prediction, which uses the realized genomic relationship or kinship matrix (K) to connect genotype to phenotype. Genomic relationship matrices share information among entries to estimate the observed entries' genetic values and predict unobserved entries' genetic values. One of the main parameters of such models is genomic variance (σg2), or the variance of a trait associated with a genome-wide sample of DNA polymorphisms, and genomic heritability (hg2); however, the seminal papers introducing different forms of K often do not discuss their effects on the model estimated variance components despite their importance in genetic research and breeding. Here, we discuss the effect of several standard methods for calculating the genomic relationship matrix on estimates of σg2 and hg2. With current approaches, we found that the genomic variance tends to be either overestimated or underestimated depending on the scaling and centering applied to the marker matrix (Z), the value of the average diagonal element of K, and the assortment of alleles and heterozygosity (H) in the observed population. Using the average semivariance, we propose a new matrix, KASV, that directly yields accurate estimates of σg2 and hg2 in the observed population and produces best linear unbiased predictors equivalent to routine methods in plants and animals.

Indexed as

Models, GeneticMultifactorial InheritanceAllelesAnimalsGenomicsGenotypePhenotypePlant BreedingPolymorphism, Single Nucleotideaverage semivariancegenomic best linear unbiased predictorgenomic heritabilitygenomic relatednessgenomic variancelinear mixed model

Identifiers

PMID35442424
PMCPMC9157152
OpenAlexW4224228027

What OpenQuestion holds

Textmetadata
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.