Approaches to long-read sequencing in a clinical setting to improve diagnostic rate

Over the past decade, advances in genetic testing, particularly the advent of next-generation sequencing, have led to a paradigm shift in the diagnosis of molecular diseases and disorders. Despite our present collective ability to interrogate more than 90% of the human genome, portions of the genome...

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Detalles Bibliográficos
Autores principales: Sanford Kobayashi, Erica, Batalov, Serge, Wenger, Aaron M., Lambert, Christine, Dhillon, Harsharan, Hall, Richard J., Baybayan, Primo, Ding, Yan, Rego, Seema, Wigby, Kristen, Friedman, Jennifer, Hobbs, Charlotte, Bainbridge, Matthew N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548499/
https://www.ncbi.nlm.nih.gov/pubmed/36210382
http://dx.doi.org/10.1038/s41598-022-20113-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548499/
https://www.ncbi.nlm.nih.gov/pubmed/36210382
http://dx.doi.org/10.1038/s41598-022-20113-x

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