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New Product

Genomic Data Analysis Sofware


For info: 310-414-8100

Illumina’s NGS-based CytoSeq assay extends beyond traditional microarray-based cytogenetics assays for detection of copy number variation (CNV) and absence of heterozygosity (AOH), but also adds the ability to identify single nucleotide variation, all in a single assay. Coupled with BioDiscovery’s NxClinical software for analysis and interpretation of genomic events, this new solution will offer customers a powerful and cost-effective research tool for studying CNVs, AOH, and mutations in genetic disorders. NxClinical software will be offered with the CytoSeq assay, providing an easy-to-use, interactive instrument for visualization and interpretation of genomic events, directly reading CytoSeq results to process sample data and provide results.

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