NAVIFY® Mutation Profiler*

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


The emergence of next-generation sequencing (NGS) has played a major role in the shift toward precision medicine. But the amount of patient-specific data that NGS generates and the ever-growing body of knowledge that must be interpreted have proven to be as much of a challenge for healthcare facilities as an opportunity.

NAVIFY® Mutation Profiler*

Empowering next-generation sequencing clinical labs with actionable information


The emergence of next-generation sequencing (NGS) has played a major role in the shift toward precision medicine. But the amount of patient-specific data that NGS generates and the ever-growing body of knowledge that must be interpreted have proven to be as much of a challenge for healthcare facilities as an opportunity.

NAVIFY Mutation Profiler is a clinical NGS reporting solution

NAVIFY Mutation Profiler can help labs accurately and efficiently interpret the clinical significance of mutations, empowering clinicians to deliver more personalized healthcare. It has been shown to reduce the time needed to draft a curation report by 75%*, and increases reproducibility while automating the workflow of report generation¹. With NAVIFY Mutation Profiler, labs are enabled to inform on potential personalized treatment strategies in a concise, professional report for the oncologist.

NAVIFY Mutation Profiler offers:

  • Clear presentation of mutations and potential treatment options
  • Simpler, more concise reports
  • Clinical significance for thousands of the most common variants classified in accordance with Association for Molecular Pathology guidelines
  • Public annotations for millions of additional variants
  • Links to actionable therapy options supported by local drug approval agencies, clinical studies and medical guidelines

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Screen capture of NAVIFY® Mutation Profiler for NGS clinical interpretation

Making NGS clinical interpretation simpler

NAVIFY Mutation Profiler helps reduce curation time and automates report generation, allowing you to support more gene panels, cancers and mutations with:

  • Pre-configured clinical and variant summaries that help reduce the time of interpretation
  • Annotations organized in a single, focused location

Easy to use

A clinical lab workflow based on lab clinician input, NAVIFY Mutation Profiler offers a clean, intuitive user interface and an outstanding user experience.

  • Lab and variant analytics with the option to opt-in for variant classification-sharing
  • Integrations with the laboratory information system and electronic medical record via APIs

Easily communicates potential personalized treatment strategies in a concise, professional report for oncologists

Apps for NAVIFY Mutation Profiler

NAVIFY Therapy Matcher app

Understand treatment options supported by local drug approval agencies, clinical studies and medical guidelines.

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NAVIFY Clinical Trial Matcher app**

Filter and identify clinical trial opportunities based on a patient’s genomic alterations.

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Partial image of white paper cover: Precision medicine requires precision in clinical interpretation and reporting with NAVIFY® Mutation Profiler

Precision medicine requires precision in clinical interpretation and reporting

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An image of clinicians engaged in advanced diagnostics through innovative technology

Driving a better future for patients

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* NAVIFY Mutation Profiler, NAVIFY Therapy Matcher app and NAVIFY Clinical Trial Matcher app are for Research Use Only. Not for use in diagnostic procedures.
** Powered by MolecularMatch, Inc.
¹ Campan et al. (2020). ‘Evaluation of Roche NAVIFY Mutation Profiler for NGS Variant Annotation and Reporting.’ Los Angeles: University of Southern California.