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A RAPD-based identification system for calla lily cultivars (Zantedeschia spp.) was constructed after screening 60 arbitrary 10-mer primers. Using this method, two or three sequential PCR reactions enable clear identification of 12 cultivars within several days.
Random amplified polymorphic DNA (RAPD) markers were tested for the identification of nine rose cultivars and three clonal plants. All of the cultivars were identified by using only three primers. Moreover, individuals were also distinguished by unique RAPD marker bands.
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