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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...
Autores principales: | Doig, Kenneth D., Love, Christopher G., Conway, Thomas, Seleznev, Andrei, Ma, David, Fellowes, Andrew, Blombery, Piers, Fox, Stephen B. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
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 |
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