MFCNV: A New Method to Detect Copy Number Variations From Next-Generation Sequencing Data

Copy number variation (CNV) is a very important phenomenon in tumor genomes and plays a significant role in tumor genesis. Accurate detection of CNVs has become a routine and necessary procedure for a deep investigation of tumor cells and diagnosis of tumor patients. Next-generation sequencing (NGS)...

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Detalles Bibliográficos
Autores principales: Zhao, Haiyong, Huang, Tihao, Li, Junqing, Liu, Guojun, Yuan, Xiguo
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/PMC7243272/
https://www.ncbi.nlm.nih.gov/pubmed/32499814
http://dx.doi.org/10.3389/fgene.2020.00434

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243272/
https://www.ncbi.nlm.nih.gov/pubmed/32499814
http://dx.doi.org/10.3389/fgene.2020.00434

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