Ontology highlight
ABSTRACT: Introduction
Rapid genomic sequencing (rGS) in critically ill infants with suspected genetic disorders has high diagnostic and clinical utility. However, rGS has primarily been available at large referral centres with the resources and expertise to offer state-of-the-art genomic care. Critically ill infants from racial and ethnic minority and/or low-income populations disproportionately receive care in safety-net and/or community settings lacking access to state-of-the-art genomic care, contributing to unacceptable health equity gaps. VIrtual GenOme CenteR is a 'proof-of-concept' implementation science study of an innovative delivery model for genomic care in safety-net neonatal intensive care units (NICUs).Methods and analysis
We developed a virtual genome centre at a refe
SUBMITTER: D'Gama AM
PROVIDER: S-EPMC10859977 | biostudies-literature | 2024 Feb
REPOSITORIES: biostudies-literature