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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Bibliografiska uppgifter
I publikationen:Comput Struct Biotechnol J
Huvudupphovsmän: Zhang, Mucheng, Liu, Deli, Tang, Jie, Feng, Yuan, Wang, Tianfang, Dobbin, Kevin K., Schliekelman, Paul, Zhao, Shaying
Materialtyp: Artigo
Språk:Inglês
Publicerad: Research Network of Computational and Structural Biotechnology 2018
Ämnen:
Research Article
Länkar: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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