Simplify mutation interpretation
Efficiently assess mutation significance to streamline lab workflows for greater productivity.
Overview
Empowering next-generation sequencing labs with an efficient clinical reporting solution
Interpret the research and clinical significance of mutations accurately and efficiently with navify Mutation Profiler, a CE-IVD* clinical NGS reporting solution. Empower your lab to deliver concise, professional reports that inform oncologists on potential personalized treatment strategies, supporting more personalized healthcare.
Enable personalized treatment insights
Deliver concise reports that help oncologists identify personalized treatment strategies.
Automate NGS reporting workflows
Reduce curation time by up to 75% and support expanded panel and mutation analysis with automation.1
navify® Mutation Profiler
Simplifying NGS research and clinical interpretation.
Making NGS research and clinical interpretation simpler
navify Mutation Profiler enhances NGS workflows with automated reporting, pre-configured variant summaries and therapy insights. Its intuitive design and seamless integrations support labs in delivering consistent, personalized insights for precision oncology.
Automated reporting and streamlined curation
navify Mutation Profiler has been shown to reduce the time needed to draft a curation report by 75%.¹ It increases reproducibility while automating report generation workflows. The solution supports broader gene panels, cancers and mutations with pre-configured clinical and variant summaries, simplifying interpretation and saving time. Centralized annotations enable lab teams to efficiently access and interpret data for faster, more accurate insights.
Comprehensive mutation insights
Gain clear insights into mutations and potential treatment options with simpler, concise reports. navify Mutation Profiler provides research and clinical significance details for thousands of common variants, classified per Association for Molecular Pathology guidelines, plus public annotations for millions more. Labs can access links to actionable therapies supported by regulatory agencies, clinical studies and medical guidelines for informed decision-making.
Intuitive and user-friendly
Developed with lab clinician input, this solution offers a clean, intuitive interface, enhancing the lab experience and enabling clear communication of personalized treatment options in concise reports for researchers and oncologists. It includes comprehensive lab and variant analytics with optional classification-sharing and seamlessly integrates with laboratory information systems and electronic medical records via APIs, streamlining workflows and improving efficiency.
Frequently asked questions about navify Mutation Profiler
If you don’t find answers to your questions here, we’re happy to provide more information and discuss your needs in detail.
Roche Diagnostics
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- Yaung SJ, Pek A. From information overload to actionable insights: digital solutions for interpreting cancer variants from genomic testing. JMP. 2021;2(4):312–318. [DOI: 10.3390/jmp2040027].
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- *navify Mutation Profiler is CE-IVD. In the US, navify Mutation Profiler is Research Use Only (RUO). Not for use in diagnostic procedures or decisions.
- MC-CH-06768