ReviewThe plant genome2026
Molecular polymorphisms that underlie trait variation in crops: Lessons learned from soybean.
Review in The plant genome, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Molecular polymorphisms that underlie trait variation in crops: Lessons learned from soybean.The plant genome · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Genetic variation within a germplasm is important in crop improvement, providing a foundation for breeders to develop new varieties. Traits of agronomic and economic importance are often mapped to identify the genetic basis of observed phenotypes, oftentimes using quantitative trait locus (QTL) analysis. While some mapped QTLs can be directly utilized in breeding programs, others benefit from a deeper understanding of the causal genes and sequence polymorphisms for effective deployment. In this review, we examine the factors that differentiate QTL where causal DNA sequence polymorphisms can be readily identified from those where causation remains difficult to resolve. We present a case study for soybean (Glycine max (L.) Merr.), in which we surveyed the literature to find the sequence variants underlying QTL in this crop. We cataloged causal variants by type, including variations within coding and regulatory regions, transposable element insertions and deletions, epigenetic modifications, and gene content variants (e.g., copy number variants). Additionally, we discuss the impediments to gene discovery, including challenges in phenotyping, the nature of sequence polymorphisms, and the difficulty of functional validation. Finally, we highlight future opportunities in the field of gene discovery, emphasizing how advances in high-resolution mapping, near-gapless genome assemblies, pangenome resources, and genome engineering will help overcome existing barriers and accelerate the discovery of causal genes and variants underlying complex traits.
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Registered trials
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.