Company profile

Fabric Genomics

Precision Medicine & Genomics

Company profile

About Fabric Genomics

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

Primary marketPrecision Medicine & Genomics
Commercial modelCommercial information available on request
Company presenceLinkedIn X
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01 · Operating footprint

Where the Company operates

Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.

Clinical focus

  • congenital heart defects
  • genetic disorders in acutely ill infants
  • hereditary disease
  • inherited disease
  • rare idiopathic disease

Who it serves

  • Children's Hospitals
  • Commercial Labs
  • Country Genome Projects
  • Hospital Systems

Deployment & integration

Cloud Saas deployment with recorded integration context.

Geographic context

Marketsglobal · Greece · United Kingdom · United States
Company sourceOfficial website

Company milestones

Platform expansion

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

Recorded partners

  • GeneDx (acquirer)
  • Genomics England
  • Intermountain Primary Children's Hospital
  • Oxford Nanopore
  • PlumCare
  • Rady Children's Institute for Genomic Medicine

02 · Flagship portfolio

Products, workflows, and platform capabilities

Selected source-backed Company products and the available commercial context.

Clinical Interpretation Services

Full-service clinical genomic interpretation and reporting

Service · Cloud SaaSCompany source

Fabric Enterprise Platform

AI-powered genomic interpretation platform for clinical labs and hospitals

Platform · Cloud SaaSCompany source

Long Read rWGS

Oxford Nanopore long-read sequencing integration for pediatric care

Platform · Cloud SaaSCompany source

Panel Interpretation

Hereditary disease panel interpretation with automated ACMG classification

Software · Cloud SaaSCompany source

Rapid NICU/PICU WGS

Ultra-rapid whole genome sequencing for critically ill infants

Software · Cloud SaaSCompany source

WGS/WES Interpretation

Whole genome and exome sequencing interpretation for rare disease diagnosis

Software · Cloud SaaSCompany source

03 · Research intelligence

Research Intelligence evidence

Publications, preprints, clinical validation, and regulatory records in Evidence Position order.

Evidence position

Publications, clinical validation, and regulatory records connected to this Company appear here.

Research

Publications & preprints

No linked records are currently available.

Clinical validation

Clinical-trial records

No linked records are currently available.

Regulatory

Regulatory records

No linked records are currently available.

04 · Company-reported outcomes

Outcomes and case studies

Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.

98% call accuracy in prioritized top 10

Study with Rady Children's Hospital

50% diagnostic yield

Compared to industry average of 25-30%

90% accuracy for #1 candidate identification

GEM algorithm causative variant identification

95% accuracy in top 5 candidates

GEM algorithm causative variant identification

Less than 2 hours

Physician-ready report generation for whole genomes

Genomics England

Diagnostic odyssey cases for rare idiopathic disease using deep phenotype and genotype data

Diagnostic yields up to 50% compared to 25-30% industry average

Intermountain Primary Children's Hospital

Using WGS to revolutionize care for Congenital Heart Defects (CHD)

PlumCare (Greece)

Strategic partnership integrating AI with FirstSteps™ Newborn Genome Screening Program

Rady Children's Institute for Genomic Medicine

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 team

Leadership profiles and professional links from the current Company record.

Stephen Kingsmore

President and CEO

LinkedIn

06 · Company updates

Updates from Fabric Genomics

Recent articles published on Fabric Genomics's official website.

07 · HAIC coverage

Coverage and analysis

Health AI Central reporting that mentions this Company.

No HAIC coverage is currently linked to this Company.

08 · Official presence

Company sources and channels

Curated official destinations from the active Company record.

09 · Market pathway

Additional Companies in this Market

Other active Companies in the same market, selected alphabetically from the HAIC directory.

Market context

Precision Medicine & Genomics

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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10 · Pro research

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Expanded Company research is in development.

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ResearchEvidence analysis

Linked research, clinical, and regulatory source pathways.

CompanyTechnical context

Expanded product, deployment, integration, and partnership research.

MethodSource & review record

Record-level provenance and review context.

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