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...

詳細記述

保存先:
書誌詳細
出版年:Comput Struct Biotechnol J
主要な著者: Zhang, Mucheng, Liu, Deli, Tang, Jie, Feng, Yuan, Wang, Tianfang, Dobbin, Kevin K., Schliekelman, Paul, Zhao, Shaying
フォーマット: Artigo
言語:Inglês
出版事項: Research Network of Computational and Structural Biotechnology 2018
主題:
Research Article
オンライン･アクセス: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
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!

類似資料