Cargando…
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...
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: | |
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 |
Ejemplares similares
-
Clonal expansion and linear genome evolution through breast cancer progression from pre-invasive stages to asynchronous metastasis
por: Krøigård, Anne Bruun, et al.
Publicado: (2015) -
Identification of metastasis driver genes by massive parallel sequencing of successive steps of breast cancer progression
por: Krøigård, Anne Bruun, et al.
Publicado: (2018) -
Genomic Analyses of Breast Cancer Progression Reveal Distinct Routes of Metastasis Emergence
por: Krøigård, Anne Bruun, et al.
Publicado: (2017) -
Combining calls from multiple somatic mutation-callers
por: Kim, Su Yeon, et al.
Publicado: (2014) -
Comparing somatic mutation-callers: beyond Venn diagrams
por: Kim, Su Yeon, et al.
Publicado: (2013)