Publication:
A rapid whole-genome sequencing service for infants with rare diseases in the United Arab Emirates

Loading...
Thumbnail Image

Date

2023

Journal Title

Journal ISSN

Volume Title

Publisher

Research Projects

Organizational Units

Journal Issue

Abstract

Introduction: A large body of evidence now supports use of rapid whole-genome sequencing (rWGS) as a cost-effective tool for timely diagnosis and tailored management of critically ill children with rare diseases. However, efficacy has so far been demonstrated only in high-income settings, which has led to disparate implementation of and variable access to rWGS.

Description

Keywords

Whole-Genome Sequencing, Whole-Genome Sequencing Service, Rare Diseases, Infants, United Arab Emirates

Citation