Findings from precision oncology in the clinic: rare, novel variants are a significant contributor to scaling molecular diagnostics

BACKGROUND: Next generation sequencing for oncology patient management is now routine in clinical pathology laboratories. Although wet lab, sequencing and pipeline tasks are largely automated, the analysis of variants for clinical reporting remains largely a manual task. The increasing volume of seq...

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Detalles Bibliográficos
Autores principales: Doig, Kenneth D., Love, Christopher G., Conway, Thomas, Seleznev, Andrei, Ma, David, Fellowes, Andrew, Blombery, Piers, Fox, Stephen B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962530/
https://www.ncbi.nlm.nih.gov/pubmed/35346197
http://dx.doi.org/10.1186/s12920-022-01214-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962530/
https://www.ncbi.nlm.nih.gov/pubmed/35346197
http://dx.doi.org/10.1186/s12920-022-01214-y

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