Hospitals - Fabric Genomics

Interpretation and reporting solutions for In-house clinical NGS testing

Precision medicine starts here

Schedule a Demo

Fabric Genomics enables hospitals and health systems to
offer comprehensive precision medicine for all stages of life

Hereditary
Risk Screening
Happy pregnant woman holding her belly on Fabric Genomics
Diagnostic Constitutional
Panel Testing
Smiling boy holding a potted plant of flowers on Fabric Genomics

Rare Disease

Cancer patient looking into the camera smiling on Fabric Genomics

Oncology

Green pattern background on Fabric Genomics

Benefits of in-house testing

Green clock icon on Fabric Genomics

Reduce Turnaround Time

Process samples 1-2 weeks faster than send out

Green magnifying glass icon on Fabric Genomics

Increase Diagnostic Yields

Use intimate patient knowledge to improve diagnosis

Full Data Ownership

Retain genomic data for simple re-analysisand longitudinal care

Generate Revenue

Keep reimbursements payments in-house

Why
Fabric?

  • Best-in-class clinical review time for WGS/WES
  • Best-in-class diagnostics yields for rare disease
  • Single platform for panels, WGS, and WES
  • Clinical services to help you get started
Schedule a Demo

Sucess stories from leaders in precision medicine

Intermountain Healthcare has been leveraging Fabric Enterprise since 2018 for in house genomic data analysis allowing them to demonstrate a leading commitment to precision medicine:

  • Inhera family of clinical tests for BRCA1/2, breast and gynecological cancer, lynch, and colorectal cancer
  • 105 gene Heredigene Population Study

At Intermountain, Genomic data and clinical reporting are seamlessly integrated into the EMR for access by clinicians, and genetic counselors are available via telehealth to promptly assist patients with their results. 

Contact Us

Rady Children’s Hospital has been using Fabric Enterprise to improve outcomes for NICU patients since 2016. Their accomplishments include:

Record setting turnaround time: 

  • < 20 hours for rapid WGS-from blood draw to diagnosis
  • < 1 hour interpretation turnaround time
  • Project Baby Bear: 43% of patients receive a diagnosis and 31% had a change in care plan 
  • Cost saving, fewer surgeries and invasive procedures, and an average savings of ~3 hospital days per baby

 

Download Case Study

Ready to get started?

Fabric Can Support All NGS Testing

What shape does your testing take?

NGS panel testing icon

Panels

Learn More
Icon - exomes

Genomes & Exomes

Learn More