ArticleBMC plant biology2025
Core construction establishment for Ruchengbaimao tea based on SSR markers.
Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Integrated metabolomic and transcriptomic analysis of Camellia sinensis var. pubilimba 'Rucheng Baimaocha' reveals distinct flavonoid and strictinin biosynthesis.BMC plant biology · 2026Article
- SSR marker development for analysis of the genetic diversity and identification of species and infraspecific ranks in the genus Phyllostachys.BMC plant biology · 2026Article
- Biochemical Profiles, Mineral Accumulation, and Water-Soluble Fluoride Traits of 65 Tea (Plants (Basel, Switzerland) · 2026Article
- Genetic diversity and population structure of wild and cultivated Camellia tetracocca Chang assessed by ILP markers: insights for conservation of an endangered tea species.BMC plant biology · 2026Article
- Integrated analysis of phenotypic and SSR data reveals the genetic structure differentiation of wildFrontiers in plant science · 2026Article
- SSR genotyping of 200 tea (Camellia sinensis) clones obtained by selection and DNA barcoding of 12 varietal registration candidates.BMC plant biology · 2025Article
- Construction of Garlic Core Collections Based on the Agronomic Traits of 366 Germplasm Accessions.Plants (Basel, Switzerland) · 2025Article
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Authors and funding
11 authors.
Funding
Abstract
Germplasm collection and conservation requires many efforts and resources. Core collection construction could both conserve genetic diversity and improve conservation efficiency. This study investigated the genetic diversity of tea plants [Camellia sinensis (L.) O. Kuntze] collected from four regions of Rucheng using 14 simple sequence repeat (SSR) markers and constructed a core collection set. A phylogenetic tree and population structure were conducted. A core set of 28 tea plants, approximately 10% of 279 tea plant individuals, was constructed to capture the samples' maximum genetic diversity. Compared to the original collection, the retention rates of N
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