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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Comput Struct Biotechnol J
Asıl Yazarlar: Zhang, Mucheng, Liu, Deli, Tang, Jie, Feng, Yuan, Wang, Tianfang, Dobbin, Kevin K., Schliekelman, Paul, Zhao, Shaying
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Research Network of Computational and Structural Biotechnology 2018
Konular:
Research Article
Online Erişim: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
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller