We are trailblazers, tenaciously deciphering human biology.
Fabric Genomics is working to ensure precision medicine is the standard of care for all patients
Our tools enable scientists to quickly and accurately process and analyze whole genomes, exomes and gene panels. Fabric Genomics’ cutting-edge genomic data processing and advanced algorithmic tools have been licensed by over 1,000 academic institutions and clinical laboratories around the world.
Fabric Genomics can complete genetic analysis of whole genomes in less than 1 hour. Leading organizations have achieved causative candidate yields of up to 54%. Fabric Genomics’ core customers are commercial clinical laboratories, hospital core labs, country sequencing programs, and research institutions.
Timeline
Ensuring Precision Healthcare Becomes a Standard Clinical Practice
2009
Fabric Genomics founded by Martin Reese, Edward Kiruluta, John Stuelpnagel & Paul Billings
December 2013
Fabric Genomics raises $8.3M Series A round of financing and transitions focus from research to clinical market
July 2015
Fabric Genomics is selected as a primary genomic interpretation and clinical reporting provider in the UK's 100,000 Genomes Project (Genomics England)
June 2016
Fabric Genomics raises $23M Series B round of financing from renowned strategic investors
November 2017
Fabric Genomics announces expanded oncology capabilities
April 2019
Fabric Genomics launches
ACE, its scalable AI variant classification engine
Leadership
Board
In addition to Martin Reese, Fabric Genomics’ board members are:
Scientific & Medical Advisory Board
Geoffrey S. Ginsburg, MD, PhD
Duke Center for Applied Genomics and Precision Medicine & Global Genomic Medicine Collaborative