 Unique CNV Array with Whole Chromosome Uniparental Disomy (UPD) Detection from OGT
07 Sep 2010 The groundbreaking CytoSure™ ISCA UPD 4 x 180k array from Oxford Gene Technology offers the ability, for the first time, to simultaneously detect DNA copy number variation (CNV) using OGT’s ISCA consortium endorsed 4 x 180k aCGH array, along with whole chromosome uniparental disomy (UPD) using SNP probes, on a single array. The array format, ease-of-use and intuitive data interpretation via the complimentary CytoSure Interpret Software, also make the CytoSure ISCA UPD array ideal for the next stage in cytogenetic research. OGT’s unique UPD detection capability (patent pending) has been enabled by multiple rounds of SNP probe selection and validation, targeting over 6000 SNPs with evenly distributed probes, resulting in highly informative content that allows confident detection of whole chromosome UPD. Furthermore, the combined ISCA-UPD ...
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