I need rapid, actionable genomic testing without the data analysis bottlenecks.

Fabric Genomics’ AI-driven software platform enables clinical labs to uncover critical and timely genomic insights that reduce costs and save lives



Speeding up diagnostics across key clinical applications



Diagnostic Odyssey

Combine genotype and phenotype data to identify and prioritize rare disease-causing variants using machine learning

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Accelerate analysis to deliver timely, critical diagnoses for acutely ill infants

Hereditary Panels


Hereditary Panels

Leverage AI and a proprietary variant database to generate customized hereditary reports



Oncology Panels

Match cancer variants with treatments and clinical trials for physician-ready oncology reports

You're in good company

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Hospitals need to diagnose life-threatening genetic illnesses quickly and efficiently. NGS data interpretation is a critical bottleneck.

Every minute counts

In genomic testing applications, such as pediatrics, rare disease diagnosis, and oncology, time is of the essence. The sooner you can detect a problem, the more likely you’ll be able to stop it before it’s too late.

The cost of delayed detection

Slow turnaround times and diagnostic yields can have grave consequences. Undetected genetic illnesses lead to poor outcomes for your patients and substantial healthcare costs.


Powered by AI, Fabric Enterprise enables clinical genomic testing at scale for faster diagnosis and treatment


Undiagnosed genetic illnesses have significant costs for both patients and providers. Fabric Enterprise enables labs to achieve the highest diagnostic yield and the fastest turn-around times to improve patient outcomes and reduce healthcare costs.

One platform. Any test.

Leverage a single comprehensive platform to analyze any NGS test — genomes, exomes, and panels.

Automated workflows.

Reduce turn-around time and labor costs with streamlined workflows for annotating, interpreting, reporting generation, and sign-off

Higher diagnostic yields.

Identify the causative variant quickly and accurately with diagnostic yields of up to 50%, versus industry average of 25-30%

Sequence to physician-ready reports.

Deliver customizable clinical reports ready to sign out in less than 2hrs for whole genome tests.

Ready to get started?

Company updates


Implementation of Whole-Exome and Virtual Panel Testing for Rare Disease at a Children’s Hospital

Register now for this March 9th GenomeWeb webinar on lessons learned from successful clinical implementation of NGS panel testing at Cincinnati Children’s Hospital Medical Center

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Achieving Success With Next-Generation Sequencing: AI-Driven Scale and a Strong Reimbursement Strategy

Join us in this November 12th webinar with XIFIN, Inc. Learn best practices to implement and scale NGS panel testing in your lab.

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Fabric Genomics to Co-market Comprehensive Sample-to-Genomic Analysis Sequencing Solutions for Hereditary Genetics

In a step toward the full realization of genomic medicine, Fabric Genomics, a leader in AI-based genomic analysis and interpretation, has announced a co-marketing agreement that will provide translational researchers around the world with integrated sample prep to reporting workflows. Combining Roche’s newly released KAPA HyperExome Probes (RUO) with the Fabric Enterprise bioinformatics and analysis …

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AMP 2020 Virtual Meeting & Expo

November 16-20th – Join us for this year’s Association for Molecular Pathology (AMP) Virtual Education and Networking Experience. Watch the Corporate Workshop on-demand here

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American Society of Human Genetics (ASHG) 2020

October 27-30th – Visit Fabric Genomics at the world’s largest online gathering of human genetics and genomics professionals.

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Join us at the Frontiers in Pediatric Genomic Medicine Conference

September 24-25th – Visit our virtual booth and learn from international genomics leaders. See how we partnered with Rady Children’s Hospital to achieve world-record diagnostic speed in the PICU.

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TranslationalDx: Advances in Multi-omic Oncology Virtual Summit

Register now for the upcoming Translational Dx summit and see our presentation “Avoiding the common mistakes labs make when launching hereditary cancer panel tests“ Wednesday, September 23rd, 2020. 9AM-Noon PST

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