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Copy Number Variation
Whole genome copy number variation studies are performed on Illumina's iScan System using their BeadArray® technology. HD BeadChips offer researchers the flexibility to profile samples with 300,000 to 4.3 million markers in high-throughput format, and deliver dense genome-wide coverage with the most up-to-date content available from the scientific community. Strategically selected probes provide sensitive copy number variation analysis and target high-value regions of the genome associated with disease.