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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Opis bibliograficzny
Główni autorzy: 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
Format: Artigo
Język:Inglês
Wydane: Public Library of Science 2013
Hasła przedmiotowe:
Research Article
Dostęp online: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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