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        <identifier>oai:meral.edu.mm:recid/69</identifier>
        <datestamp>2021-12-13T02:19:50Z</datestamp>
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          <dc:title>Development of SSR markers to study diversity in the genus Cymbidium</dc:title>
          <dc:creator>Moe Kyaw Thu</dc:creator>
          <dc:creator>Weiguo Zhao</dc:creator>
          <dc:creator>Hong-Seon Song</dc:creator>
          <dc:creator>You-Hyen Kim</dc:creator>
          <dc:creator>Jong-Wook Chung</dc:creator>
          <dc:creator>Young-Il Cho</dc:creator>
          <dc:creator>Pue Hee Park</dc:creator>
          <dc:creator>Ha-Seung Park</dc:creator>
          <dc:creator>Soo-Cheon Chae</dc:creator>
          <dc:creator>Yong-Jin Park</dc:creator>
          <dc:description>Cymbidium spp. are important potted flowers with extremely high ornamental and&#13; economic value. The present study reports the development of 14 new simple sequence&#13; repeat (SSR) markers through the construction of an enriched Cymbidium goeringii library&#13; and cross-amplification in Cymbidium sinensis and Cymbidium hybridium. Of 525, 322&#13; (61.33%) clones had SSR motifs and among motifs di-nucleotides were predominant and&#13; followed by tri-nucleotide and tetra-nucleotide type. In polymorphic analysis using 14&#13; newly developed SSRs, a total of 201 alleles across 96 Cymbidium accessions were detected&#13; with an average of 14.4 per locus. The average heterozygosity was 0.394. The average gene&#13; diversity and polymorphism information content values were 0.394 and 0.639, respectively.&#13; The mean genetic similarity coefficient was 0.4297, indicating a wide genetic variation&#13; among the Cymbidium accessions. These newly developed SSRs will be useful tools&#13; for genotype identification, germplasm conservation, molecular breeding, and assessments&#13; of genetic diversity and population structure in Cymbidium.</dc:description>
          <dc:date>2010-07</dc:date>
          <dc:identifier>http://hdl.handle.net/20.500.12678/0000000069</dc:identifier>
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