VHVT: An ultra-sensitive somatic mutation detection and performance assessment program
Journal of Clinical Oncology, pp. 1588-1588, 2017.
1588Background: NGS as a high throughput technique is particular valuable for cancer given its ability to detect multiple driver mutations. While reads contain SNVs and short InDels can be mapped to the right position using gatk-like programs, a program designed for germline mutation detection, reads contain long InDels such as EGFR EX19 ...More
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