ArticlePlants (Basel, Switzerland)2021
Development of SSR Databases Available for Both NGS and Capillary Electrophoresis in Apple, Pear and Tea.
Article in Plants (Basel, Switzerland), 2021. 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, 12 citations in OpenAlex.
- Pear scab resistance gene Rvn1 from Ussurian pear is located in a cluster of receptor-like protein ethylene-inducing Xylanase (EIX) genes.BMC plant biology · 2025Article
- First Assembly of a Draft Genome of the Critically Endangered Northern Muriqui (Ecology and evolution · 2025Article
- Simple Sequence Repeat-Based Genetic Diversity Analysis of Alfalfa Varieties.International journal of molecular sciences · 2025Article
- Power of Short Tandem Repeat (STR) Analysis for Analysis of Genetic Differences and Genotype Identification.Methods in molecular biology (Clifton, N.J.) · 2025Article
- Simple Sequence Repeat Fingerprint Identification of Essential-Oil-BearingBiomolecules · 2023Article
- Multiple-Genome-Based Simple Sequence Repeat Is an Efficient and Successful Method in Genotyping and Classifying Different Jujube Germplasm Resources.Plants (Basel, Switzerland) · 2023Article
- Rapid and easy construction of a simplified amplicon sequencing (simplified AmpSeq) library for marker-assisted selection.Scientific reports · 2023Article
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Developing new varieties in fruit and tea breeding programs is very costly and labor-intensive. Thus, establishing a variety discrimination system is important for protecting breeders' rights and producers' profits. Simple sequence repeat (SSR) databases that can be utilized for both next-generation sequencing (SSR-GBS) and polymerase chain reaction-capillary electrophoresis (PCR-CE) would be very useful in variety discrimination. In the present study, SSRs with tri-, tetra- and pentanucleotide repeats were examined in apple, pear and tea. Out of 37 SSRs that showed clear results in PCR-CE, 27 were suitable for SSR-GBS. Among the remaining markers, there was allele dropout for some markers that caused differences between the results of PCR-CE and SSR-GBS. For the selected 27 markers, the alleles detected by SSR-GBS were comparable to those detected by PCR-CE. Furthermore, we developed a computational pipeline for automated genotyping using SSR-GBS by setting a value "α" for each marker, a criterion whether a genotype is homozygous or heterozygous based on allele frequency. The set of 27 markers contains 10, 8 and 9 SSRs for apple, pear and tea, respectively, that are useful for both PCR-CE and SSR-GBS and suitable for automation. The databases help researchers discriminate varieties in various ways depending on sample size, markers and methods.
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