HBOS-CNV: A New Approach to Detect Copy Number Variations From Next-Generation Sequencing Data

Copy number variation (CNV) is a genomic mutation that plays an important role in tumor evolution and tumor genesis. Accurate detection of CNVs from next-generation sequencing (NGS) data is still a challenging task due to artifacts such as uneven mapped reads and unbalanced amplitudes of gains and l...

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Detalles Bibliográficos
Autores principales: Guo, Yang, Wang, Shuzhen, Yuan, Xiguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215577/
https://www.ncbi.nlm.nih.gov/pubmed/34163521
http://dx.doi.org/10.3389/fgene.2021.642473

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215577/
https://www.ncbi.nlm.nih.gov/pubmed/34163521
http://dx.doi.org/10.3389/fgene.2021.642473

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