Evidence map›Paper›PMID 34115154›Full record

ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2021

Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments.

Elaheh Vojgani, Torsten Pook, Johannes W R Martini, Armin C Hölker, Manfred Mayer, Chris-Carolin Schön, Henner Simianer

Abstract read
In one paragraph

Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 2021. 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
–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

11 citing papers in PubMed.

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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

7 authors.

Elaheh VojganiCenter for Integrated Breeding Research, Animal Breeding and Genetics Group, University of Goettingen, Goettingen, Germany. vojgani@gwdg.de.ORCID http://orcid.org/0000-0003-4375-3531
Torsten PookCenter for Integrated Breeding Research, Animal Breeding and Genetics Group, University of Goettingen, Goettingen, Germany.
Johannes W R MartiniInternational Maize and Wheat Improvement Center (CIMMYT), Texcoco, State of Mexico, Mexico.
Armin C HölkerPlant Breeding, TUM School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany.
Manfred MayerPlant Breeding, TUM School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany.
Chris-Carolin SchönPlant Breeding, TUM School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany.
Henner SimianerCenter for Integrated Breeding Research, Animal Breeding and Genetics Group, University of Goettingen, Goettingen, Germany.

Funding

BMBF 031B0195
6 · The paper itself

Abstract

key messageThe accuracy of genomic prediction of phenotypes can be increased by including the top-ranked pairwise SNP interactions into the prediction model. We compared the predictive ability of various prediction models for a maize dataset derived from 910 doubled haploid lines from two European landraces (Kemater Landmais Gelb and Petkuser Ferdinand Rot), which were tested at six locations in Germany and Spain. The compared models were Genomic Best Linear Unbiased Prediction (GBLUP) as an additive model, Epistatic Random Regression BLUP (ERRBLUP) accounting for all pairwise SNP interactions, and selective Epistatic Random Regression BLUP (sERRBLUP) accounting for a selected subset of pairwise SNP interactions. These models have been compared in both univariate and bivariate statistical settings for predictions within and across environments. Our results indicate that modeling all pairwise SNP interactions into the univariate/bivariate model (ERRBLUP) is not superior in predictive ability to the respective additive model (GBLUP). However, incorporating only a selected subset of interactions with the highest effect variances in univariate/bivariate sERRBLUP can increase predictive ability significantly compared to the univariate/bivariate GBLUP. Overall, bivariate models consistently outperform univariate models in predictive ability. Across all studied traits, locations and landraces, the increase in prediction accuracy from univariate GBLUP to univariate sERRBLUP ranged from 5.9 to 112.4 percent, with an average increase of 47 percent. For bivariate models, the change ranged from -0.3 to + 27.9 percent comparing the bivariate sERRBLUP to the bivariate GBLUP, with an average increase of 11 percent. This considerable increase in predictive ability achieved by sERRBLUP may be of interest for "sparse testing" approaches in which only a subset of the lines/hybrids of interest is observed at each location.

Indexed as

EnvironmentEpistasis, GeneticModels, GeneticPhenotypeQuantitative Trait LociChromosome MappingChromosomes, PlantPolymorphism, Single NucleotideZea mays

Identifiers

PMID34115154
PMCPMC8354961

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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.