Home | Fabric Genomics

Turning odysseys
into answers

Genomic Interpretation
software that unlocks diagnosis

Partners & Customers

Clinical interpretation, not just data analysis

Most NGS interpretation platforms go from sequencing data to variant lists.

Fabric Enterprise automates the whole review process, recommending just
1 or a few causative variants

90%
Faster
clinical review
15min
WGS/WES
analysis
94.6%
Pathogenic variant classification for panels

Speeding up diagnostics across key clinical applications

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

NICU / PICU

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

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

Dr. Stephen Kingsmore headshot

Accuracy, usability and speed are critical in the applicaiton of genetic interpertation, which is why we chose to work with [Fabric Genomics] as a key partner in the process.

Dr. Stephen Kingsmore, President and CEO, Rady Children’s Institute for Genomic Medicine

Ready to get started?

Company updates

News

Events

ACMG 2021 Virtual Meeting

April 13-16th – Join us for this year’s ACMG Annual Clinical Genetics Meeting in a fully virtual format and watch our Product Theaters presentation.

Stay in the loop

Follow us on social media for updates