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...

Descripción completa

Detalles Bibliográficos
Autores principales: Budczies, Jan, Pfarr, Nicole, Romanovsky, Eva, Endris, Volker, Stenzinger, Albrecht, Denkert, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Software
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

Internet

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

Ejemplares similares