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...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
הוצא לאור ב: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.
פורמט: Artigo
שפה:Inglês
יצא לאור: BioMed Central 2017
נושאים:
Software
גישה מקוונת: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
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