A global platform for clinical genomic data analysis

Fabric Genomics (formerly Omicia) delivers a robust set of computational genomic capabilities to clinical labs and population sequencing initiatives in more than 50 countries.

Fabric Genomics delivers clinical-grade data analysis with unprecedented speed and quality

  • Up to 54%

    causative candidate yield

    Industry-leading data insights to improve clinical decision-making

  • 1-Hour

    turnaround time for whole genome annotation

    Premium “STAT” rapid annotation service for clinical cases

  • +1,000

    research and clinical licenses

    Leading genomic data analysis software and advanced algorithmic tools used by academic institutions and clinical laboratories around the world

  • 20-50x

    faster variant calling vs. GATK

    Easy-to-deploy best practice workflow for secondary analysis

Partnered with World-Class Labs, Health Systems & Country Projects

The Latest from Fabric Genomics

Fabric Genomics has partnered with Genomics England’s 100,000 Genomes Project, Rady Children’s Institute for Genomic Medicine (RCIGM), and The Utah Genome Project (UGP), to provide fast and accurate identification of pediatric disease-causing variants to improve the clinical care of children. Fabric Genomics’ Opal™ Clinical is the only genomic interpretation and reporting platform to include the algorithms VAAST and Phevor, two pioneering …

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ASHG 2017

Orlando, FL
October 17-21

Booth #513

Clinical Co-Lab Educational Talk: Wed. Oct. 18

Data Co-Lab Educational Talk: Thurs. Oct. 19

For Meetings, Contact: info@fabricgenomics.com