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CNViz: An R/Shiny Application for Interactive Copy Number Variant Visualization in Cancer
Copy number variants (CNVs) comprise a class of mutation which includes deletion, duplication, or amplification events that range in size from smaller than a single-gene or exon, to the size of a full chromosome. These changes can affect gene expression levels and are thus implicated in disease, inc...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888957/ https://www.ncbi.nlm.nih.gov/pubmed/35251754 http://dx.doi.org/10.1016/j.jpi.2022.100089 |