aCNViewer: Comprehensive genome-wide visualization of absolute copy number and copy neutral variations

MOTIVATION: Copy number variations (CNV) include net gains or losses of part or whole chromosomal regions. They differ from copy neutral loss of heterozygosity (cn-LOH) events which do not induce any net change in the copy number and are often associated with uniparental disomy. These phenomena have...

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Detalles Bibliográficos
Autores principales: Renault, Victor, Tost, Jörg, Pichon, Fabien, Wang-Renault, Shu-Fang, Letouzé, Eric, Imbeaud, Sandrine, Zucman-Rossi, Jessica, Deleuze, Jean-François, How-Kit, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736239/
https://www.ncbi.nlm.nih.gov/pubmed/29261730
http://dx.doi.org/10.1371/journal.pone.0189334

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736239/
https://www.ncbi.nlm.nih.gov/pubmed/29261730
http://dx.doi.org/10.1371/journal.pone.0189334

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