Our Pathology Workbench is an end-to-end solution that integrates directly with lab sequencers, annotates detected variants, brings back potential clinical trials and therapies, and produces a comprehensive summary report. We help pathology labs validate their new assays, and scale their test volume through easy variant analysis and comprehensive support for large panels, such as TSO 500. Our solution is also a process enhancement tool that enables users to go from order entry to quality control to variant analysis and reporting, quickly and easily.
We help you easily analyze and interpret raw genomic data.
GenomOncology's Pathology Workbench enables molecular pathology labs to easily process, validate, and report their genomic testing results into actionable information for clinicians.
WHAT WE ENABLE YOU TO DO
OUR WORKBENCH IN USE
In 2015, the Fred & Pamela Buffet Cancer Center at UNMC launched GenomOncology’s Pathology Workbench to streamline its reporting workflow providing easy-to-interpret genomic results to clinicians.
The Pathology Workbench has been integrated with the Personalis ACE Platform, reducing delivery time for clinical reports by several days, and returning potentially actionable results to physicians faster.
Emory is using our Pathology Workbench to enable precision oncology by connecting disparate tools and databases and allowing data to flow end to end to aid case workflow and create actionable reports.