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...

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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404673/
https://www.ncbi.nlm.nih.gov/pubmed/28438193
http://dx.doi.org/10.1186/s13073-017-0427-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404673/
https://www.ncbi.nlm.nih.gov/pubmed/28438193
http://dx.doi.org/10.1186/s13073-017-0427-z

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