Evidence map›Paper›PMID 40684039›Full record

ArticleHeredity2025

Machine learning reveals complex genetics of fungal resistance in sorghum grain mold.

Ezekiel Ahn, Louis K Prom, Sunchung Park, Dongho Lee, Jishnu Bhatt, Vishnutej Ellur, Seunghyun Lim, Jae Hee Jang, Dilip Lakshman, Clint Magill

Abstract read
In one paragraph

Article in Heredity, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. A haplotype-layered GWAS identifies a multi-trait grain mold resistance hub on sorghum chromosome 5.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2026
    Article
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

10 authors.

Ezekiel AhnSustainable Perennial Crops Laboratory, Agricultural Research Service, United States Department of Agriculture, Beltsville, MD, USA. ezekiel.ahn@usda.gov.ORCID 0000-0003-4447-4104
Louis K PromInsect Control and Cotton Disease Research, Agricultural Research Service, Southern Plains Agricultural Research Center, United States Department of Agriculture, College Station, TX, USA.
Sunchung ParkSustainable Perennial Crops Laboratory, Agricultural Research Service, United States Department of Agriculture, Beltsville, MD, USA.
Dongho LeeSoybean Genomics & Improvement Laboratory, Agricultural Research Service, United States Department of Agriculture, Beltsville, MD, USA.
Jishnu BhattSustainable Perennial Crops Laboratory, Agricultural Research Service, United States Department of Agriculture, Beltsville, MD, USA.
Vishnutej EllurMolecular Plant Sciences, Washington State University, Pullman, WA, USA.
Seunghyun LimSustainable Perennial Crops Laboratory, Agricultural Research Service, United States Department of Agriculture, Beltsville, MD, USA.
Jae Hee JangSustainable Perennial Crops Laboratory, Agricultural Research Service, United States Department of Agriculture, Beltsville, MD, USA.
Dilip LakshmanMolecular Plant Pathology Laboratory, Agricultural Research Service, United States Department of Agriculture, Beltsville, MD, USA.ORCID 0000-0002-7454-8605
Clint MagillDepartment of Plant Pathology and Microbiology, Texas A&M University, College Station, TX, USA.

Funding

USDA 8042-21000-303-000-DUSDA 8042-21220-258-000-D
6 · The paper itself

Abstract

Plant disease resistance is often a complex, polygenic trait, making its genetic dissection with traditional genome-wide association studies (GWAS) challenging. Grain mold in sorghum, a devastating disease caused by a fungal complex, exemplifies this complexity. We hypothesized that a machine learning (ML)-driven GWAS, employing diverse phenotypic representations from a panel of 306 sorghum accessions, could more effectively unravel the genetic basis of resistance. Phenotypic data, including raw disease scores, a 'difference phenotype' (inoculated vs. control), and principal components, were analyzed using Boosted Tree and Bootstrap Forest models, demonstrating strong explanatory power for phenotypic variance when trained on the entire dataset. This ML-GWAS approach confirmed a highly polygenic architecture for grain mold resistance, identifying numerous SNPs across the sorghum genome. Notably, several SNPs were consistently associated with resistance across multiple analytical models and phenotypic representations. These robustly identified SNPs were frequently located near genes with predicted functions integral to plant defense. Gene ontology (GO) analyses of the candidate gene set confirmed enrichment in categories supporting roles in pathogen recognition, DNA repair, and stress response modulation, indicating a multifaceted defense mechanism. This study provides valuable candidate genes for breeding sorghum with enhanced grain mold resistance and offers a refined methodological framework for dissecting complex traits in this crop. The successful application of this ML-based strategy in sorghum suggests its potential utility for studying similar complex traits in other plant species.

Indexed as

Disease ResistanceMachine LearningPlant DiseasesSorghumGenome-Wide Association StudyMultifactorial InheritancePhenotypePolymorphism, Single Nucleotide

Identifiers

PMID40684039
PMCPMC12317092

What Socratic holds

Textmetadata
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 Socratic graph.