Article
A three-caller pipeline for variant analysis of cancer whole-exome sequencing data.
Molecular medicine reports - 1 May 2017
Liu Ze-Kun, Shang Yu-Kui, Chen Zhi-Nan, Bian Huijie
Abstract excerpt
Rapid advancements in next generation sequencing (NGS) technologies, coupled with the dramatic decrease in cost, have made NGS one of the leading approaches applied in cancer research. In addition, it is increasingly used in clinical practice for cancer diagnosis and treatment. Somatic (cancer‑only) single nucleotide variants and small insertions and deletions (indels) are the simplest classes of mutation,...
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