global platform for clinical genomics
Fabric Genomics empowers
clinical labs with
comprehensive genomic
insights for hereditary
disease
and oncology
News & Events
Satellite Workshop:
Accurate and Rapid Genome Interpretation in Clinical Care
June 17, 15:00–16:30 hrs
(Amber 1)
Booth #364. For Meetings, Contact:
info@fabricgenomics.com
Fabric at Work
Investigating Genetic Variants on a Large Scale in Large Population Studies and Country Genome Projects
The Genomics England’s 100,000 Genomes Project is a ground-breaking, country sequencing program that focuses on cancer and rare diseases. It is the largest and most prestigious population genome sequencing project of its kind. Fabric’s Genomics’ Clinical tool …
Learn More 
Rapid Whole Genome Interpretation of Pediatric Patients in the NICU/PICU
Rady Children’s Institute for Genomic Medicine in San Diego (RCIGM) uses Fabric Genomics’ software for clinical interpretation and reporting of disease-causing variants in critically-ill children admitted to neonatal and pediatric intensive care units (NICU/PICU). Stephen Kingsmore, …
Learn More 
Flexible Platform for Genome Analysis
Laboratory Corporation of America® Holdings (LabCorp®) uses Fabric Genomics’ platform for its clinical trials sequencing services. LabCorp’s broad menu of testing services, combined with Fabric Genomics’ flexible, powerful, and easy-to-use genome analysis platform, will allow the companies …
Learn More 
Partnering with Researchers on Case-Control and Cohort Studies
Fabric’s robust variant classification software relies on publicly available algorithms and also our proprietary algorithms such as VAAST (The Variant Annotation, Analysis & Search Tool) and Phevor (Phenotype Driven Variant Ontological Re-ranking tool), which were co-developed by …
Learn MoreClinical-grade Data Analysis with Unprecedented Speed and Quality
Up to 54%
causative candidate yield
Industry-leading data insights to improve clinical decision-making
<2 hours
turnaround time
Whole genome interpretation and reporting with Premium “STAT” service for clinical cases
>25,000
clinical cases interpreted
Best-in-class clinical-grade software
for clinical interpretation
+1,000
research and clinical licenses
Leading genomic data analysis software and advanced algorithmic tools used globally
Partners
Leading the Way to a Healthier World
Oncology
8.2 million people worldwide die annually from cancer (World Health Organization). Inherited genetic mutations play a major role in 5 to 10 percent of all cancers. Genomic data analysis for both somatic and hereditary cancer is available using Fabric Genomics’ tools.
Reference: NIH: National Cancer InstitutePediatrics
~33% of infants admitted to NICU have an underlying genetic disease. Fabric Genomics’ STAT pediatric clinical genome offering provides a 1-hour turnaround time for clinicians, patients, and their families.
Reference: Infant DNA test Speeds Diagnosis of Rare Diseases, New York Times, October 3, 2012, 4 Saunders et al, Science Translational Medicine, 2012, 4(154);1-13Women's Health
~50% of women with BRCA1/2 mutations will develop breast cancer by the age of 70. Fabric Genomics’ automated panel reporting tools deliver critical insights for clinical labs and oncologists.
Reference: CDC KnowYourBRCACardio & Metabolic
17.5 million people worldwide die annually from cardiovascular disease. In certain populations, 5-8% of babies are born with a genetic or partly genetic disease and up to 30% are born with genetically-driven metabolic disease. Fabric Genomics is working with scientists within country genome programs to build anonymized patient cohorts to mine genotype and phenotype data for discovery purposes.
Reference: World Health Organization and ScienceNeurology
1 in 4 people worldwide will be affected by neurological disorders (World Health organization). In Western countries, it’s estimated that about five to seven people per 100,000 are affected by Huntington’s Disease. Fabric Genomics works with partners to perform whole genome analysis to support research in precision medicine.
Reference: World Health OrganizationRegulatory Compliance & Security
