A remark on copy number variation detection methods

Copy number variations (CNVs) are gain and loss of DNA sequence of a genome. High throughput platforms such as microarrays and next generation sequencing technologies (NGS) have been applied for genome wide copy number losses. Although progress has been made in both approaches, the accuracy and cons...

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Detalles Bibliográficos
Autores principales: Li, Shuo, Dou, Xialiang, Gao, Ruiqi, Ge, Xinzhou, Qian, Minping, Wan, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5922522/
https://www.ncbi.nlm.nih.gov/pubmed/29702671
http://dx.doi.org/10.1371/journal.pone.0196226

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