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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...
Tallennettuna:
| Julkaisussa: | BMC Bioinformatics |
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| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2018
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| 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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