Evaluation of Nine Somatic Variant Callers for Detection of Somatic Mutations in Exome and Targeted Deep Sequencing Data

Next generation sequencing is extensively applied to catalogue somatic mutations in cancer, in research settings and increasingly in clinical settings for molecular diagnostics, guiding therapy decisions. Somatic variant callers perform paired comparisons of sequencing data from cancer tissue and ma...

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Detalles Bibliográficos
Autores principales: Krøigård, Anne Bruun, Thomassen, Mads, Lænkholm, Anne-Vibeke, Kruse, Torben A., Larsen, Martin Jakob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4803342/
https://www.ncbi.nlm.nih.gov/pubmed/27002637
http://dx.doi.org/10.1371/journal.pone.0151664

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4803342/
https://www.ncbi.nlm.nih.gov/pubmed/27002637
http://dx.doi.org/10.1371/journal.pone.0151664

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