Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinic

Abstract Background Diagnosis of rare genetic diseases can be a long, expensive and complex process, involving an array of tests in the hope of obtaining an actionable result. Long-read sequencing platforms offer the opportunity to make definitive molecular diagnoses using a single assay capable of...

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Detalhes bibliográficos

Principais autores:	Stephanie U. Greer, Jacquelin Botello, Donna Hongo, Brynn Levy, Premal Shah, Matthew Rabinowitz, Danny E. Miller, Kate Im, Akash Kumar
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMC 2023-06-01
coleção:	Journal of Translational Medicine
Assuntos:	Long-read sequencing Oxford Nanopore Technologies Adaptive sampling Copy number variants Neurodevelopmental disorders Clinical testing
Acesso em linha:	https://doi.org/10.1186/s12967-023-04243-y
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