Fabric Oncology Panels

Translating genomic insights into targeted cancer therapies

Enabling precision medicine by leveraging Fabric’s proprietary annotation and comprehensive clinical interpretation engine.

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Rapid 
Turnaround Time

Drug and Trial Matching

Sequence to 
Clinical Report

Testimonial

We enable laboratories around the world to detect biomarkers for the diagnosis and treatment of cancer. [Our partnership] offers clinical laboratories everything they need to conduct tumor profiling, from tumor DNA to report, and can be up and running and ready to begin validation in under a week.

WOLFGANG DAUM, President and CEO, TOMA Biosciences

Enabling personalized cancer treatment decisions by combining a robust bioinformatics and reporting platform with actionable clinical content.

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Rapid Turnaround Time

Reduce the time you spend identifying actionable cancer aberrations by accessing clinically actionable information inside the Fabric system. With configurable workflows and lab-specific roles, labs can average less than 30 minutes turnaround time for pre-curated panels.

Drug and Trial Matching

Match cancer genomic alterations to regularly updated targeted therapies, clinical trials, and clinical guideline information in order to generate physician-ready clinical reports. A single, seamless application provides access to clinically actionable information for SNVs, InDels, and structural variants across solid tumor and hematology panels.

Sequence to Clinical Report

With a secondary analysis pipeline optimized for somatic cancer variants, start with a FASTQ file and easily review QC metrics. Cancer-specific annotation and curation inside efficient SOP-based workflows enable rapid generation of physician-ready clinical reports.

Partners

Discover how Fabric Genomics can help your lab succeed 
with NGS testing