CNV-PCC: An efficient method for detecting copy number variations from next-generation sequencing data

Copy number variations (CNVs) significantly influence the diversity of the human genome and the occurrence of many complex diseases. The next-generation sequencing (NGS) technology provides rich data for detecting CNVs, and the read depth (RD)-based approach is widely used. However, low CN (copy num...

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Detalles Bibliográficos
Autores principales: Zhang, Tong, Dong, Jinxin, Jiang, Hua, Zhao, Zuyao, Zhou, Mengjiao, Yuan, Tianting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Bioengineering and Biotechnology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751350/
https://www.ncbi.nlm.nih.gov/pubmed/36532569
http://dx.doi.org/10.3389/fbioe.2022.1000638

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751350/
https://www.ncbi.nlm.nih.gov/pubmed/36532569
http://dx.doi.org/10.3389/fbioe.2022.1000638

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