PSCC: Sensitive and Reliable Population-Scale Copy Number Variation Detection Method Based on Low Coverage Sequencing

BACKGROUND: Copy number variations (CNVs) represent an important type of genetic variation that deeply impact phenotypic polymorphisms and human diseases. The advent of high-throughput sequencing technologies provides an opportunity to revolutionize the discovery of CNVs and to explore their relatio...

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Detalles Bibliográficos
Autores principales: Li, Xuchao, Chen, Shengpei, Xie, Weiwei, Vogel, Ida, Choy, Kwong Wai, Chen, Fang, Christensen, Rikke, Zhang, Chunlei, Ge, Huijuan, Jiang, Haojun, Yu, Chang, Huang, Fang, Wang, Wei, Jiang, Hui, Zhang, Xiuqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897425/
https://www.ncbi.nlm.nih.gov/pubmed/24465483
http://dx.doi.org/10.1371/journal.pone.0085096

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897425/
https://www.ncbi.nlm.nih.gov/pubmed/24465483
http://dx.doi.org/10.1371/journal.pone.0085096

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