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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Detalhes bibliográficos
Publicado no:Comput Struct Biotechnol J
Main Authors: Zhang, Mucheng, Liu, Deli, Tang, Jie, Feng, Yuan, Wang, Tianfang, Dobbin, Kevin K., Schliekelman, Paul, Zhao, Shaying
Formato: Artigo
Idioma:Inglês
Publicado em: Research Network of Computational and Structural Biotechnology 2018
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6154469/
https://ncbi.nlm.nih.gov/pubmed/30258547
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.csbj.2018.09.001
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