Rapid whole-genome sequencing in critically Ill children: shifting from unease to evidence, education, and equitable implementation
Abstract
In his editorial, Lantos incorrectly claimed poor protocol adherence because many eligible patients were not enrolled.1Lantos J.D. Sources of unease about the use of genome sequencing for diagnosing rare diseases in children.J Pediatr. 2021; 237: 13-15Abstract Full Text Full Text PDF PubMed Scopus (1) Google Scholar Project Baby Bear was a quality improvement project implementing rapid whole-genome sequencing (rWGS) in infants receiving Medicaid...
Paper Details
Title
Rapid whole-genome sequencing in critically Ill children: shifting from unease to evidence, education, and equitable implementation
Published Date
Nov 1, 2021
Journal
Volume
238
Pages
343 - 343
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Notes
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