Evidence map›Paper›PMID 35069614›Full record

ArticleFrontiers in plant science2021

Genomic Selection for Wheat Blast in a Diversity Panel, Breeding Panel and Full-Sibs Panel.

Philomin Juliana, Xinyao He, Felix Marza, Rabiul Islam, Babul Anwar, Jesse Poland, Sandesh Shrestha, Gyanendra P Singh, Aakash Chawade, Arun K Joshi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in plant science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.8field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Reinforced Defenses:International journal of molecular sciences · 2025
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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

12 authors at 8 institutions in 5 countries.

Philomin JulianaBorlaug Institute for South Asia (BISA), Ludhiana, India.
Xinyao HeInternational Maize and Wheat Improvement Center (CIMMYT), Mexico, Mexico.
Felix MarzaInstituto Nacional de Innovación Agropecuaria y Forestal (INIAF), La Paz, Bolivia.
Rabiul IslamBangladesh Wheat and Maize Research Institute (BWMRI), Dinajpur, Bangladesh.
Babul AnwarBangladesh Wheat and Maize Research Institute (BWMRI), Dinajpur, Bangladesh.
Jesse PolandDepartment of Plant Pathology, Wheat Genetics Resource Center, Kansas State University, Manhattan, KS, United States.
Sandesh ShresthaDepartment of Plant Pathology, Wheat Genetics Resource Center, Kansas State University, Manhattan, KS, United States.
Gyanendra P SinghIndian Council of Agricultural Research (ICAR)-Indian Institute of Wheat and Barley Research, Karnal, India.
Aakash ChawadeDepartment of Plant Breeding, Swedish University of Agricultural Sciences, Alnarp, Sweden.
Arun K JoshiBorlaug Institute for South Asia (BISA), Ludhiana, India.
Ravi P SinghInternational Maize and Wheat Improvement Center (CIMMYT), Mexico, Mexico.
Pawan K SinghInternational Maize and Wheat Improvement Center (CIMMYT), Mexico, Mexico.
Centro Internacional de Mejoramiento de Maíz Y Trigo · MXBangladesh Wheat and Maize Research Institute · BDKansas State University · USBorlaug Institute for South Asia · INIndian Council of Agricultural Research · INInstituto Nacional de Innovación Agropecuaria y ForestalInternational Maize and Wheat Improvement Center · INSwedish University of Agricultural Sciences · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wheat blast is an emerging threat to wheat production, due to its recent migration to South Asia and Sub-Saharan Africa. Because genomic selection (GS) has emerged as a promising breeding strategy, the key objective of this study was to evaluate it for wheat blast phenotyped at precision phenotyping platforms in Quirusillas (Bolivia), Okinawa (Bolivia) and Jashore (Bangladesh) using three panels: (i) a diversity panel comprising 172 diverse spring wheat genotypes, (ii) a breeding panel comprising 248 elite breeding lines, and (iii) a full-sibs panel comprising 298 full-sibs. We evaluated two genomic prediction models (the genomic best linear unbiased prediction or GBLUP model and the Bayes B model) and compared the genomic prediction accuracies with accuracies from a fixed effects model (with selected blast-associated markers as fixed effects), a GBLUP + fixed effects model and a pedigree relationships-based model (ABLUP). On average, across all the panels and environments analyzed, the GBLUP + fixed effects model (0.63 ± 0.13) and the fixed effects model (0.62 ± 0.13) gave the highest prediction accuracies, followed by the Bayes B (0.59 ± 0.11), GBLUP (0.55 ± 0.1), and ABLUP (0.48 ± 0.06) models. The high prediction accuracies from the fixed effects model resulted from the markers tagging the 2NS translocation that had a large effect on blast in all the panels. This implies that in environments where the 2NS translocation-based blast resistance is effective, genotyping one to few markers tagging the translocation is sufficient to predict the blast response and genome-wide markers may not be needed. We also observed that marker-assisted selection (MAS) based on a few blast-associated markers outperformed GS as it selected the highest mean percentage (88.5%) of lines also selected by phenotypic selection and discarded the highest mean percentage of lines (91.8%) also discarded by phenotypic selection, across all panels. In conclusion, while this study demonstrates that MAS might be a powerful strategy to select for the 2NS translocation-based blast resistance, we emphasize that further efforts to use genomic tools to identify non-2NS translocation-based blast resistance are critical.

Indexed as

blast diseasegenomic selection (GS)genotyping-by sequencingMagnaporthe oryzaemarker-assisted selectionpedigree selectionwheat

Identifiers

PMID35069614
PMCPMC8782147
OpenAlexW4205279474

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.