A Single Cell Level Based Method for Copy Number Variation Analysis by Low Coverage Massively Parallel Sequencing

Copy number variations (CNVs), a common genomic mutation associated with various diseases, are important in research and clinical applications. Whole genome amplification (WGA) and massively parallel sequencing have been applied to single cell CNVs analysis, which provides new insight for the fields...

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Detalhes bibliográficos
Main Authors: Zhang, Chunlei, Zhang, Chunsheng, Chen, Shengpei, Yin, Xuyang, Pan, Xiaoyu, Lin, Ge, Tan, Yueqiu, Tan, Ke, Xu, Zhengfeng, Hu, Ping, Li, Xuchao, Chen, Fang, Xu, Xun, Li, Yingrui, Zhang, Xiuqing, Jiang, Hui, Wang, Wei
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3553135/
https://ncbi.nlm.nih.gov/pubmed/23372689
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0054236
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