NAVIFY® Mutation Profiler*

Extend the power of NAVIFY Mutation Profiler


NAVIFY Clinical Decision Support apps ecosystem makes valuable information easily accessible, enabling clinical lab teams to provide more informed personalized treatment strategies and patient care decisions.

NAVIFY® Mutation Profiler*

Extend the power of NAVIFY Mutation Profiler


NAVIFY Clinical Decision Support apps ecosystem makes valuable information easily accessible, enabling clinical lab teams to provide more informed personalized treatment strategies and patient care decisions.

NAVIFY Therapy Matcher app

Provides clinical significance of detected variants and cancer indications by:

  • Informing treatment options (if applicable) based on publicly available information, such as approved drug labels, medical guidelines and clinical trial outcomes
  • Providing clinical and preclinical evidence supporting clinical significance of the variant based on publicly available information, such as biomedical literature
  • Engaging practitioners managing patient care and/or clinical laboratory members (e.g., molecular geneticists, clinical lab directors)
  • Linking identified mutations to approved treatment options
  • Obtaining treatment options based on clinical implications of variant combinations

NAVIFY Clinical Trial Matcher app**

  • Easily identify clinical trial opportunities based on an individual patient’s genomic alterations
  • Query and present matching trials from ClinicalTrials.gov, as well as other international trial registries and private institutions
  • Filter clinical trials relevant to particular variants, location, gender and desired phase
Software solutions

NAVIFY Mutation Profiler*

Empowering next-generation sequencing
clinical research labs with actionable
information.

Learn more

* Research Use Only in the United States. Not for use in diagnostic procedures.
** Powered by MolecularMatch, Inc.