Health Systems

Fabric Genomics supports data analysis, interpretation and reporting for panels, exomes, and genomes for both hereditary diseases and somatic cancer. For Health Systems, Fabric Genomics’ tools easily integrate with hospital EMRs to deliver actionable genomic results within physician workflow at point-of-care.

  • Rapid turnaround time
  • Integrated ACMG guideline classification
  • Standard protocols & test workflows
  • API for EMR & LIMS integration
  • Secure & CAP/CLIA compliant programs
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Fabric Genomics' Solutions for Health Systems

Hereditary Disease

  • Launch in-house panel, exome or whole genome testing
  • Accelerate turnaround time with our classified variant database – automatically improves with use
  • Deploy standard lab protocols to ensure accuracy and consistency at scale
  • Use panel builder to quickly create and curate standard panels to speed reporting
  • Analyze FASTQ or BAM files to generate VCFs with our secondary analysis pipeline


  • Fabric Genomics’ oncology solution supports testing for whole gene or hotspot panels, and exomes
  • Report on solid tumor and hematology cases
  • Interpret SNVs and indels as well as structural variants and CNVs
  • Perform molecular and clinical interpretation, with accurate and up-to-date clinical information including approved drugs and clinical trials specific to the patient’s cancer
  • Support molecular tumor board reviews
  • Comply with AMP 2017 classification guidelines

Pediatric Clinical Genomes

  • Automated secondary and tertiary analysis tools for whole genome interpretation and clinical reporting
  • Fabric Genomic’s STAT product yields fully annotated whole genomes within 1 hour, for urgent cases
  • Fabric Genomic’s expert network of clinical genomic scientists available for case interpretation including escalation of difficult cases
  • Structural variant detection for difficult or undiagnosed cases using BioGraph

Storage and Requery

  • Maintain a long-term genomic patient data repository that can be queried and analyzed for on-going patient care
  • Use advanced data compression to encrypt and store BAM and FASTQ data at half of the size of the original BAM file

Key Value to Your Health System


  • EMR and LIMS integration
  • Rapid turnaround times for patient treatment
  • Holistic genetic view of patients
  • Standard workflows and protocols
  • Integrated ACMG guideline classification
  • CAP/CLIA compliant programs
  • HIPAA compliant programs to protect patient privacy

Partnered with World-Class Health Systems

Key Benefits


Achieve cost efficiencies, significantly reduce turnaround time and store genetic data for optimal decision support.

Integrate Patient
Data Easily

Bring genomic data into physician workflow via EMR/LIMS system integrations, securely streamline the sharing and access to hosted patient-level data. Re-query in silico panels as needed for decision support.

Thought Leadership
and Patient Outcomes

Improve patient care and outcomes by establishing hospital or system as precision medicine center. Reduce burden on patients, families, and caregivers by delivering rapid genetic insights.