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Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/609
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dc.contributor.authorSiju, S-
dc.contributor.authorDhanya, K-
dc.contributor.authorSyamkumar, S-
dc.contributor.authorSasikumar, B-
dc.contributor.authorSheeja, T E-
dc.contributor.authorBHAT, A I-
dc.contributor.authorPARTHASARATHY, V A-
dc.date.accessioned2017-10-09T05:47:39Z-
dc.date.available2017-10-09T05:47:39Z-
dc.date.issued2010-02-
dc.identifier.citationMol Biotechnol, February 2010, Volume 44, Issue 2, pp 140–147en_US
dc.identifier.urihttp://hdl.handle.net/123456789/609-
dc.description.abstractExpressed sequence tags (ESTs) from turmeric (Curcuma longa L.) were used for the screening of type and frequency of Class I (hypervariable) simple sequence repeats (SSRs). A total of 231 microsatellite repeats were detected from 12,593 EST sequences of turmeric after redundancy elimination. The average density of Class I SSRs accounts to one SSR per 17.96 kb of EST. Mononucleotides were the most abundant class of microsatellite repeat in turmeric ESTs followed by trinucleotides. A robust set of 17 polymorphic EST–SSRs were developed and used for evaluating 20 turmeric accessions. The number of alleles detected ranged from 3 to 8 per loci. The developed markers were also evaluated in 13 related species of C. longa confirming high rate (100%) of cross species transferability. The polymorphic microsatellite markers generated from this study could be used for genetic diversity analysis and resolving the taxonomic confusion prevailing in the genus.en_US
dc.subjectCross species amplificationen_US
dc.subjectCurcuma longa Len_US
dc.subjectExpressed sequence tagsen_US
dc.subjectMicrosatellite markersen_US
dc.subjectTurmericen_US
dc.titleDevelopment, Characterization and Cross Species Amplification of Polymorphic Microsatellite Markers from Expressed Sequence Tags of Turmeric (Curcuma longa L.)en_US
dc.typeArticleen_US
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