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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...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:BMC Bioinformatics
Päätekijät: Budczies, Jan, Pfarr, Nicole, Romanovsky, Eva, Endris, Volker, Stenzinger, Albrecht, Denkert, Carsten
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2018
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5921540/
https://ncbi.nlm.nih.gov/pubmed/29699497
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-018-2159-5
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