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...

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Detalles Bibliográficos
Autores principales: Ramesh, Rebecca G., Bigdeli, Ashkan, Rushton, Chase, Rosenbaum, Jason N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Original Research Article
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

Internet

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

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