Deliver actionable information from your NGS analysis based on a highly curated evidence-based knowledge base. NAVIFY® Mutation Profiler helps labs accurately and efficiently interpret the clinical significance of mutations, empowering clinicians to deliver more personalized healthcare.
Confidently, clearly, and efficiently interpret the clinical significance of mutations
Discover all treatment options, based on publicly available information, medical guidelines, and clinical trial outcomes
Easily identify clinical trial opportunities based on genomic alterations of an individual patient
Precision medicine requires precision in clinical interpretation and reporting. With NAVIFY® Mutation Profiler, our lab has access to the most clinically relevant and up-to-date information, drastically reducing our curation time. The intuitive software produces concise, actionable reports that accelerate our clinicians’ ability to deliver the best treatment options for our patients.
Institute for hematopathology Hamburg
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Matthias Bodmer
Disease Area Manager Oncology
