New NGS assay delivers exceptional coverage, providing a rapid and highly sensitive means of investigating MRD in AML samples
Read articleNew NGS assay delivers exceptional coverage, providing a rapid and highly sensitive means of investigating MRD in AML samples
ReadFueled by cutting-edge clinical and genomic data, partnership provides intuitive and fully customizable reporting capabilities for all conditions
ReadCollaboration will enable users to readily and simply interpret variant calls made by OGT’s NGS software via the Intelliseq iFlow™ engine.
ReadEnhanced NGS portfolio includes Interpret Software updates and enables rapid and confident variant detection even in difficult-to-sequence regions.
ReadExpansion of access to clinical support network and market-leading genomic solutions aims to improve patient outcomes.
ReadNew leadership will drive OGT’s mission to improve clinical care by partnering with customers.
ReadCytoCell University offers extensive FISH expertise and reaffirms commitment to customer support and training.
ReadNew integrated website, expanded resources and substantial worldwide support reaffirm partnership and commitment to customers.
ReadIn the workshop users will explain how OGT’s SureSeq™ NGS panels can increase throughput and save time and cost in the detection of a wide variety of aberrations.
ReadLaunch of two NGS panels enables comprehensive detection of genetic abnormalities involved in breast and ovarian cancer, and myeloid disorders.
ReadPaper published in npj Genomic Medicine demonstrates identification of more reportable CNVs with CytoSure v3 vs traditional array design.
ReadAddition of direct-sales territories follows successes across Europe and APAC and provides customers with enhanced local sales and support services.
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