Press Releases August 24, 2022 Novel Newborn Screening System Uses Rapid Whole Genome Sequencing and Acute Management Guidance to Screen and Diagnosis Genetic Diseases Study demonstrates feasibility of NBS-rWGS prototype to rapidly screen for several hundred genetic diseases with effective interventions
Press Releases July 26, 2022 Study Supports Potential of Genome-to-Treatment (GTRx™) to Guide Physicians in the Management of 500 Treatable Genetic Diseases
Media Coverage July 25, 2022 The earlier the better: New consortium leverages infant screening to accelerate treatment PharmaVoice PHARMAVOICE: Newborn screening is gaining prominence across the biopharma and healthcare industries amid efforts to detect and treat disease as early as possible.
Press Releases June 14, 2022 RCIGM Launches Program to Advance Newborn Screening for Treatable Genetic Diseases
Media Coverage October 21, 2021 Artificial Intelligence Can Rapidly Diagnose Rare Genetic Diseases Medscape
Media Coverage October 14, 2021 Study Shows Fabric’s GEM AI Improves Rare Disease Diagnosis Clinical OMICs
Press Releases October 14, 2021 Benchmark Genome Study Demonstrates Accuracy of Artificial Intelligence in Rapidly Diagnosing Rare Diseases in Critically Ill Patients