Confirming variants discovered by Next Generation Sequencing (NGS) with Sanger sequencing using innovative bioinformatics tools

被引：0
|
作者：
Schreiber, E. [1 ]
Berosik, S. [1 ]
Wenz, M. [1 ]
Chang, S. [1 ]
Jackson, S. [1 ]
Zhai, J. [1 ]
Schneider, S. [1 ]
Brzoska, P. [1 ]
机构：
[1] Thermo Fisher Sci, Div Genet Sci, San Francisco, CA USA
来源：
EUROPEAN JOURNAL OF CANCER | 2016年 / 61卷
关键词：
D O I：
10.1016/S0959-8049(16)61054-7
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
136
引用
收藏
页码：S19 / S19
页数：1
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