cnvCurator: an interactive visualization and editing tool for somatic copy number variations

BACKGROUND: One of the most important somatic aberrations, copy number variations (CNVs) in tumor genomes is believed to have a high probability of harboring oncotargets. Detection of somatic CNVs is an essential part of cancer genome sequencing analysis, but the accuracy is usually limited due to v...

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Detalles Bibliográficos
Autores principales: Ma, Lingnan, Qin, Maochun, Liu, Biao, Hu, Qiang, Wei, Lei, Wang, Jianmin, Liu, Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608136/
https://www.ncbi.nlm.nih.gov/pubmed/26472134
http://dx.doi.org/10.1186/s12859-015-0766-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608136/
https://www.ncbi.nlm.nih.gov/pubmed/26472134
http://dx.doi.org/10.1186/s12859-015-0766-y

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