Detecting somatic point mutations in cancer genome sequencing data: a comparison of mutation callers

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作者
Qingguo Wang
Peilin Jia
Fei Li
Haiquan Chen
Hongbin Ji
Donald Hucks
Kimberly Brown Dahlman
William Pao
Zhongming Zhao
机构
[1] Vanderbilt University School of Medicine,Department of Biomedical Informatics
[2] Center for Quantitative Sciences,State Key Laboratory of Cell Biology
[3] Vanderbilt University Medical Center,Department of Thoracic Surgery
[4] Institute of Biochemistry and Cell Biology,Department of Oncology
[5] Shanghai Institutes for Biological Sciences,Department of Cancer Biology
[6] Chinese Academy of Sciences,Department of Medicine/Division of Hematology
[7] Fudan University Shanghai Cancer Center,Oncology
[8] Shanghai Medical College,Department of Psychiatry
[9] Vanderbilt-Ingram Cancer Center,undefined
[10] Vanderbilt University Medical Center,undefined
[11] Vanderbilt University School of Medicine,undefined
[12] Vanderbilt University School of Medicine,undefined
[13] Vanderbilt University School of Medicine,undefined
来源
Genome Medicine | / 5卷
关键词
Normal Sample; Lung Cancer Cell Line; Whole Exome Sequencing; Alternate Allele; Next Generation Sequencing Data;
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