KNNCNV: A K-Nearest Neighbor Based Method for Detection of Copy Number Variations Using NGS Data

Copy number variation (CNV) is a well-known type of genomic mutation that is associated with the development of human cancer diseases. Detection of CNVs from the human genome is a crucial step for the pipeline of starting from mutation analysis to cancer disease diagnosis and treatment. Next-generat...

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Detalles Bibliográficos
Autores principales: Xie, Kun, Liu, Kang, Alvi, Haque A K, Chen, Yuehui, Wang, Shuzhen, Yuan, Xiguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728060/
https://www.ncbi.nlm.nih.gov/pubmed/35004691
http://dx.doi.org/10.3389/fcell.2021.796249

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728060/
https://www.ncbi.nlm.nih.gov/pubmed/35004691
http://dx.doi.org/10.3389/fcell.2021.796249

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