PATHOLOGY WORKBENCH
Our Pathology Workbench is an end-to-end solution that integrates directly with lab sequencers, annotates detected variants, brings back potential clinical trials, and produces a comprehensive summary report. We help pathology labs scale their test volume through easy variant analysis and comprehensive support for large panels. Our solution is also a process enhancement tool that enables users to go from order entry to QC to variant analysis and reporting easily and quickly.
We help you easily analyze and interpret raw genomic data.
OUR SOLUTION
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
Easy Integration
Our tool has the flexibility to integrate with your current technology infrastructure, including NGS sequencers, laboratory information management systems (LIMS), EHRs, etc.
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Multiple Test Modes
Our tool supports the analysis of multiple test modes including NGS, CNV, Gene Fusions, Cytogenetics, IHC, etc. Our tool can also report and support MSI and TMB results
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Clinical Trial Matching
Our Pathology Workbench enables you to review clinical trials generated from the combination of every “significant” variant including untested biomarkers and variants from all test types/modes.
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Clinical Decision Support
Our Pathology Workbench is integrated with FDA, NCCN, ASCO and Vanderbilt University's My Cancer Genome data in order to provide you with knowledge-driven clinical decision support
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Supports AMP tiers
Our tool is integrated with clinical guidelines and classification tiers from the Association of Molecular Pathologists (AMP) to provide more support for variant interpretations
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Trust but Verify
Our software verifies your BAM files for hotspot regions that may have been missed by a variant caller to provide a second check so that you see a complete list of results within the tool.
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OUR PROCESS
The Pathology Workbench provides you with recommendations to pass or fail a run based on sample level QC metrics defined by your assay validation metrics. This information can be tracked to help comply with CAP guidelines and can be exported for audit purposes.
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The Pathology Workbench presents you with the information required to review variants (read counts, quality info, BAM cartoon, pile-ups, platform recommendation, etc.) while providing relevant clinical interpretations. All information is presented in a single view for a comprehensive and streamlined analysis.
The Pathology Workbench enables flexible template-driven reporting for a variety of different use cases. The final report is fully customizable both in presentation and format. These report can be easily integrated into any EMR/LIS tool for full traceability.
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OUR WORKBENCH IN USE
UNIVERSITY OF
NEBRASKA MEDICINE
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.
PERSONALIS
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 HEALTHCARE
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
