SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data

BACKGROUND: Targeted next-generation sequencing (NGS) has been widely used as a cost-effective way to identify the genetic basis of human disorders. Copy number variations (CNVs) contribute significantly to human genomic variability, some of which can lead to disease. However, effective detection of...

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Gepubliceerd in:BMC Bioinformatics
Hoofdauteurs: Chen, Yong, Zhao, Li, Wang, Yi, Cao, Ming, Gelowani, Violet, Xu, Mingchu, Agrawal, Smriti A., Li, Yumei, Daiger, Stephen P., Gibbs, Richard, Wang, Fei, Chen, Rui
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2017
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Methodology Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5335817/
https://ncbi.nlm.nih.gov/pubmed/28253855
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1566-3
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