SEG - A Software Program for Finding Somatic Copy Number Alterations in Whole Genome Sequencing Data of Cancer

As next-generation sequencing technology advances and the cost decreases, whole genome sequencing (WGS) has become the preferred platform for the identification of somatic copy number alteration (CNA) events in cancer genomes. To more effectively decipher these massive sequencing data, we developed...

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Detalles Bibliográficos
Autores principales: Zhang, Mucheng, Liu, Deli, Tang, Jie, Feng, Yuan, Wang, Tianfang, Dobbin, Kevin K., Schliekelman, Paul, Zhao, Shaying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154469/
https://www.ncbi.nlm.nih.gov/pubmed/30258547
http://dx.doi.org/10.1016/j.csbj.2018.09.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154469/
https://www.ncbi.nlm.nih.gov/pubmed/30258547
http://dx.doi.org/10.1016/j.csbj.2018.09.001

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