Can Rapid Nanopore Sequencing Bring Genomic Testing to the Bedside?
Author:
Affiliation:
1. Victorian Clinical Genetics Services, Murdoch Children’s Research Institute , Melbourne, Victoria , Australia
2. University of Melbourne , Melbourne , Australia
3. Australian Genomics , Melbourne , Australia
Publisher
Oxford University Press (OUP)
Subject
Biochemistry (medical),Clinical Biochemistry
Link
https://academic.oup.com/clinchem/article-pdf/68/12/1484/47615813/hvac111.pdf
Reference5 articles.
1. Integrating genomics into healthcare: a global responsibility;Stark;Am J Hum Genet,2019
2. Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing;Goenka
3. Ultrarapid nanopore genome sequencing in a critical care setting;Gorzynski;N Engl J Med,2022
4. Rapid genomic testing for critically ill children: time to become standard of care?;Stark;Eur J Hum Genet,2022
5. Feasibility of ultra-rapid exome sequencing in critically ill infants and children with suspected monogenic conditions in the Australian public health care system;Lunke;JAMA,2020
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