Evidence map›Paper›PMID 30455185›Full record

ArticleG3 (Bethesda, Md.)2019

Prediction of Subgenome Additive and Interaction Effects in Allohexaploid Wheat.

Nicholas Santantonio, Jean-Luc Jannink, Mark Sorrells

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.7field-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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. '1347B' module confers durable stripe rust resistance in wheat.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2026
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  4. Harnessing big data for enhanced genome-wide prediction in winter wheat breeding.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 3 institutions in 1 country.

Nicholas SantantonioCornell University, Plant Breeding and Genetics Section, School of Integrated Plant Sciences, College of Agriculture and Life Sciences, 240 Emerson Hall, Ithaca, NY 14853 and ns722@cornell.edu.ORCID 0000-0002-4351-4023
Jean-Luc JanninkCornell University, Plant Breeding and Genetics Section, School of Integrated Plant Sciences, College of Agriculture and Life Sciences, 240 Emerson Hall, Ithaca, NY 14853 and.ORCID 0000-0003-4849-628X
Mark SorrellsCornell University, Plant Breeding and Genetics Section, School of Integrated Plant Sciences, College of Agriculture and Life Sciences, 240 Emerson Hall, Ithaca, NY 14853 and.ORCID 0000-0002-7367-2663
Cornell University · USNew York State College of Agriculture & Life Sciences · USRobert W. Holley Center for Agriculture & Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whole genome duplications have played an important role in the evolution of angiosperms. These events often occur through hybridization between closely related species, resulting in an allopolyploid with multiple subgenomes. With the availability of affordable genotyping and a reference genome to locate markers, breeders of allopolyploids now have the opportunity to manipulate subgenomes independently. This also presents a unique opportunity to investigate epistatic interactions between homeologous orthologs across subgenomes. We present a statistical framework for partitioning genetic variance to the subgenomes of an allopolyploid, predicting breeding values for each subgenome, and determining the importance of inter-genomic epistasis. We demonstrate using an allohexaploid wheat breeding population evaluated in Ithaca, NY and an important wheat dataset from CIMMYT previously shown to demonstrate non-additive genetic variance. Subgenome covariance matrices were constructed and used to calculate subgenome interaction covariance matrices for variance component estimation and genomic prediction. We propose a method to extract population structure from all subgenomes at once before covariances are calculated to reduce collinearity between subgenome estimates. Variance parameter estimation was shown to be reliable for additive subgenome effects, but was less reliable for subgenome interaction components. Predictive ability was equivalent to current genomic prediction methods. Including only inter-genomic interactions resulted in the same increase in accuracy as modeling all pairwise marker interactions. Thus, we provide a new tool for breeders of allopolyploid crops to characterize the genetic architecture of existing populations, determine breeding goals, and develop new strategies for selection of additive effects and fixation of inter-genomic epistasis.

Indexed as

Epistasis, GeneticGenome, PlantPolyploidySoftwareGenomicsTriticumAllopolyploidyEpistasisGenomic predictionHeterosis

Identifiers

PMID30455185
PMCPMC6404612
OpenAlexW2950129738

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.