PSCC: sensitive and reliable population-scale copy number variation detection method based on low coverage sequencing.

PSCC: sensitive and reliable population-scale copy number variation detection method based on low coverage sequencing.

<h4>Background</h4>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 ex...

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Bibliographic Details
Main Authors: Xuchao Li, Shengpei Chen, Weiwei Xie, Ida Vogel, Kwong Wai Choy, Fang Chen, Rikke Christensen, Chunlei Zhang, Huijuan Ge, Haojun Jiang, Chang Yu, Fang Huang, Wei Wang, Hui Jiang, Xiuqing Zhang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24465483/?tool=EBI

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https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24465483/?tool=EBI

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