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Analyze actionable mutations in the EGFR pathway Cell3™ Target: Actionable Mutation panel (EGFR) Detect low frequency variants in key oncogenes of the Epidermal Growth Factor Receptor (EGFR) pathway using genomic DNA (gDNA) or cell-free DNA (cfDNA) from primary tumors or liquid biopsies. Request a quote Product Datasheet Clinically relevant content A highly focused panel covering…

Terms and Conditions When we do business with you, the standard terms and conditions below are an important part of the contract between you, the customer, and Nonacus. They set out each of our legal rights and responsibilities, and other information required by law. Some important points are: Purchase orders must quote the relevant design…

Careers at Nonacus Formed by a dedicated group of biotechnology professionals, Nonacus understands the need for laboratories to continually deliver progress. This understanding forms the basis of all our products and drives our innovation. View Current Roles Why Nonacus? Our core values stem from being patient and customer centric, collaborative and innovative in our approach.…

Panel Design Tool Create custom next generation sequencing (NGS) panels online in minutes. Start your design Your design in your hands Complete design control Our online software means you can create a panel design, get target coverage information and request a quote in minutes. Flexible input files From BED files, gene lists or genomic coordinates,…

Custom NGS panels for rare variant detection Cell3™ Target: Custom Oncology Panels Targeted resequencing using innovative Cell3 Target technology to convert cell-free DNA (cfDNA), genomic (gDNA) and formalin fixed paraffin embedded (FFPE) DNA into libraries for next generation sequencing (NGS). Request a quote Product datasheet Validated for FFPE and ctDNA samples Developed for and validated…

Carrier Screening for pediatric recessive disorders Cell3™ Target: Carrier Screening panel Accurately analyze carrier status of 448 inherited childhood disorders using a single workflow. Request a quote Comprehensive content Designed to enrich for genes with high clinical significance in a broad range of rare, highly penetrant recessive childhood disorders. Streamlined workflow Consolidate multiple technology workflows…