ArticleThe plant genome2026
Diverse reference genomes detect variants in the US winter wheat.
Article 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.
- Diverse reference genomes detect variants in the US winter wheat.The plant genome · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
The first hexaploid bread wheat reference genome from Chinese Spring was released in 2018 by the International Wheat Genome Sequencing Consortium and is considered as the industry standard reference. To explore the effects of different reference genomes on variant discovery, 29 hexaploid bread wheat (Triticum aestivum L.) cultivars from the Southern Great Plains of the United States with varying whole genome sequencing depth were aligned to three reference genomes. The reference genomes varied in evolutionary similarity to the cohort of the germplasm analyzed: (1) Jagger, a Kansas State University cultivar, a reference with high similarity, (2) Chinese Spring, a Chinese landrace, the current industry standard, (3) Durum-tauschii, an "in silico" hybridization of the reference genomes of tetraploid durum wheat and wild Aegilops tauschii, for an unrepresentative reference. The Jagger reference genome retained more informative variants after filtering. Synteny regions and large introgressions were identified by read alignment coverage, using diverse reference genomes to identify lines containing Aegilops ventricosa (2N
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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.