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Ioncopy: an R Shiny app to call copy number alterations in targeted NGS data
BACKGROUND: Somatic copy number alterations (CNAs) contribute to the clinically targetable aberrations in the tumor genome. For both routine diagnostics and biomarkers research, CNA analysis in a single assay together with somatic mutations is highly desirable. RESULTS: Ioncopy is a validated method...
Autores principales: | Budczies, Jan, Pfarr, Nicole, Romanovsky, Eva, Endris, Volker, Stenzinger, Albrecht, Denkert, Carsten |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921540/ https://www.ncbi.nlm.nih.gov/pubmed/29699497 http://dx.doi.org/10.1186/s12859-018-2159-5 |
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