A survey of somatic genome deletions and HBV DNA insertions in a Hepatocellular Carcinoma (HCC) case
Variation in genome structure is an important source of human genetic polymorphism. The findings from studies of somatic Insertions/deletions promise to provide insights into cancer biology. We can profit by understanding the structural variation in human tumorigenesis. Next-generation sequencing supports the possibility to survey the specific somatic Insertions/deletions on a whole genome scale in tumors.
JunCai
Beijing Institute of Genomics, Chinese Academy of Sciences, China, 100029
国际会议
杭州
英文
23-24
2010-10-01(万方平台首次上网日期,不代表论文的发表时间)