DeAnnCNV: a tool for online detection and annotation of copy number variations from whole-exome sequencing data

With the decrease in costs, whole-exome sequencing (WES) has become a very popular and powerful tool for the identification of genetic variants underlying human diseases. However, integrated tools to precisely detect and systematically annotate copy number variations (CNVs) from WES data are still i...

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Detalles Bibliográficos
Autores principales: Zhang, Yuanwei, Yu, Zhenhua, Ban, Rongjun, Zhang, Huan, Iqbal, Furhan, Zhao, Aiwu, Li, Ao, Shi, Qinghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Web Server issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489280/
https://www.ncbi.nlm.nih.gov/pubmed/26013811
http://dx.doi.org/10.1093/nar/gkv556

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489280/
https://www.ncbi.nlm.nih.gov/pubmed/26013811
http://dx.doi.org/10.1093/nar/gkv556

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