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Detecting viral sequences in NGS data.
Cantalupo, Paul G; Pipas, James M.
Afiliación
  • Cantalupo PG; Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.
  • Pipas JM; Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA. Electronic address: pipas@pitt.edu.
Curr Opin Virol ; 39: 41-48, 2019 12.
Article en En | MEDLINE | ID: mdl-31465960
ABSTRACT
Next generation sequencing (NGS) technologies provide an increasingly important avenue for detecting known viruses, and for discovering novel viruses present in clinical or environmental samples. Several computational pipelines capable of identifying and classifying viral sequences in NGS data have been developed and used to search for viruses in human or animal samples, microbiomes, and in various environments. In this review we summarize the different approaches used to determine viral presence in sequence data. Strategies for avoiding confounding factors such as physical contamination and computational artifacts that lead to false virus identification are discussed. The application of these methodologies to cancer data sets has led to important insights on viruses both as drivers of and biomarkers for specific tumors.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Virus / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Curr Opin Virol Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Virus / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Curr Opin Virol Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos