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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Bibliografiske detaljer
Udgivet i:Nucleic Acids Res
Main Authors: Zhang, Yuanwei, Yu, Zhenhua, Ban, Rongjun, Zhang, Huan, Iqbal, Furhan, Zhao, Aiwu, Li, Ao, Shi, Qinghua
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2015
Fag:
Web Server issue
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4489280/
https://ncbi.nlm.nih.gov/pubmed/26013811
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkv556
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