PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories

BACKGROUND: The increasing affordability of DNA sequencing has allowed it to be widely deployed in pathology laboratories. However, this has exposed many issues with the analysis and reporting of variants for clinical diagnostic use. Implementing a high-throughput sequencing (NGS) clinical reporting...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:Genome Med
Main Authors: Doig, Kenneth D., Fellowes, Andrew, Bell, Anthony H., Seleznev, Andrei, Ma, David, Ellul, Jason, Li, Jason, Doyle, Maria A., Thompson, Ella R., Kumar, Amit, Lara, Luis, Vedururu, Ravikiran, Reid, Gareth, Conway, Thomas, Papenfuss, Anthony T., Fox, Stephen B.
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2017
Assuntos:
Software
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5404673/
https://ncbi.nlm.nih.gov/pubmed/28438193
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-017-0427-z
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares