RKDOSCNV: A Local Kernel Density-Based Approach to the Detection of Copy Number Variations by Using Next-Generation Sequencing Data

Copy number variations (CNVs) are significant causes of many human cancers and genetic diseases. The detection of CNVs has become a common method by which to analyze human diseases using next-generation sequencing (NGS) data. However, effective detection of insignificant CNVs is still a challenging...

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Detalles Bibliográficos
Autores principales: Liu, Guojun, Zhang, Junying, Yuan, Xiguo, Wei, Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673372/
https://www.ncbi.nlm.nih.gov/pubmed/33329705
http://dx.doi.org/10.3389/fgene.2020.569227

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673372/
https://www.ncbi.nlm.nih.gov/pubmed/33329705
http://dx.doi.org/10.3389/fgene.2020.569227

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