Clinical Interpretation Services
Full-service clinical genomic interpretation and reporting
Company profile
Company profile
Fabric Genomics is making precision medicine a reality by facilitating clinical labs, hospital systems, and country-sequencing programs to develop, deploy, and scale genomic testing. The company's flagship Fabric Enterprise platform leverages advanced AI algorithms to automate genomic data interpretation and generate physician-ready clinical reports for any genomic test. Fabric's technology addresses the major bottleneck in genetic testing: interpretation and report generation as test volumes rapidly increase. The platform combines deep phenotype data with genotype data using machine learning to accurately identify and prioritize disease-causing variants in rare idiopathic diseases. Fabric's AI approach includes proprietary algorithms such as GEM, VAAST, Phevor, and VVP that systematically prioritize variants based on severity in conjunction with patient phenotype. The company serves children's hospitals, hospital systems, and commercial laboratories worldwide, supporting applications including hereditary risk screening, rare disease diagnosis, rapid NICU testing, pediatric panels, and country genome projects. Fabric's cloud-based solution can scale from a single test to hundreds of thousands while maintaining high accuracy and rapid turnaround times. The company has achieved diagnostic yields up to 50% compared to the industry average of 25-30%, with the ability to generate clinical reports in less than two hours for whole genome sequence data. In a significant milestone, GeneDx acquired Fabric Genomics to expand decentralized, AI-powered testing at global scale.
Company description Fabric Genomics official website
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01 · Operating footprint
Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.
Cloud Saas deployment with recorded integration context.
Company milestones
GeneDx acquired Fabric Genomics to expand decentralized, AI-powered testing at global scale; Oxford Nanopore and Fabric Genomics launched integrated WGS Pediatric Care Solution for long-read WGS in NICU/PICU applications; PlumCare and Fabric announced strategic partnership integrating AI with FirstSteps newborn genome screening program in Greece
Partnerships
02 · Flagship portfolio
Selected source-backed Company products and the available commercial context.
Full-service clinical genomic interpretation and reporting
AI-powered genomic interpretation platform for clinical labs and hospitals
Oxford Nanopore long-read sequencing integration for pediatric care
Hereditary disease panel interpretation with automated ACMG classification
Ultra-rapid whole genome sequencing for critically ill infants
Whole genome and exome sequencing interpretation for rare disease diagnosis
03 · Research intelligence
Publications, preprints, clinical validation, and regulatory records in Evidence Position order.
Publications, clinical validation, and regulatory records connected to this Company appear here.
Research
No linked records are currently available.
Clinical validation
No linked records are currently available.
Regulatory
No linked records are currently available.
04 · Company-reported outcomes
Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.
Study with Rady Children's Hospital
Compared to industry average of 25-30%
GEM algorithm causative variant identification
GEM algorithm causative variant identification
Physician-ready report generation for whole genomes
Diagnostic odyssey cases for rare idiopathic disease using deep phenotype and genotype data
Diagnostic yields up to 50% compared to 25-30% industry average
Using WGS to revolutionize care for Congenital Heart Defects (CHD)
Strategic partnership integrating AI with FirstSteps™ Newborn Genome Screening Program
Rapid whole genome sequencing for critically ill infants in NICU/PICU to diagnose genetic disorders
98% call accuracy in prioritized top 10 variants, physician-ready reports in less than 2 hours for whole genomes
05 · Leadership
Leadership profiles and professional links from the current Company record.
Stephen Kingsmore
President and CEO
06 · Company updates
Recent articles published on Fabric Genomics's official website.
07 · HAIC coverage
Health AI Central reporting that mentions this Company.
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08 · Official presence
Curated official destinations from the active Company record.
09 · Market pathway
Other active Companies in the same market, selected alphabetically from the HAIC directory.
Market context
Companies using AI to analyze genomic, proteomic, metabolomic, or multi-omics data to provide personalized treatment recommendations, identify genetic risks, or develop targeted therapies. Includes genomic sequencing platforms with AI analysis, preventive medicine based on genetic risk assessment, and longevity care based on molecular and genetic data.
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