Fabric Enterprise

A single comprehensive platform for NGS data analysis and clinical reporting for hereditary panels, somatic cancer panels, and whole genomes

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The Platform

Fabric Clinical Idiopathic

Combining deep phenotype data with genomic data using proven proprietary algorithms to rapidly and accurately identify disease-causing variants in rare disease patients.

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Fabric Clinical

Combining the benefits of proven variant prioritization algorithms with the latest in cloud computing to enable the accelerated interpretation of genetic tests in time-critical situations.

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Fabric Hereditary Panels

Providing automated, accurate interpretation by leveraging Fabric’s proprietary annotation engine and classified variant knowledge base.

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Fabric Oncology Panels

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

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Enabling precision medicine through algorithm guided assessment of NGS data in inherited disease and oncology.

Fabric Enterprise Key Benefits


Security and Regulatory Compliance

Cloud and on-site hosting options incorporating comprehensive data and network security protocols. Regulatory compliance programs.

  • Industry-standard data encryption
  • HIPAA and SSAE 16
  • ISO 27001
  • FDA 21 CFR part 11 and Part 820
  • CLIA and CAP

Secure and Scalable

A solution that scales with your lab as you launch new assays and grow in test volume.

  • Easily launch targeted panel, exome, and genome based tests
  • High-throughput workflows for every test type that enable your lab to scale

One Platform, Any Test

A single comprehensive platform that can support all of your NGS testing needs–spanning diagnostic and risk-based tests in multiple disease areas.

  • Inherited Cancer Risk
  • Carrier Screening
  • Hereditary Disease Testing
  • Molecular Oncology
  • Rare/Idiopathic Disease

Algorithmic Advantage

Algorithms, technology, and clinical standards to drive scientific accuracy and efficiency.

  • Variant prioritization algorithms for individuals, families, or population cohort analysis
  • Access to an expert network of variant scientists
  • Machine learning methods that leverage our large classified variant database to accelerate interpretation and reporting

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