CancerVar: A New Bioinformatics Tool Developed for Clinical Interpretation of Cancer Mutations
XTalks
MAY 10, 2022
CancerVar will help researchers standardize and automate clinical interpretations for 13 million somatic mutations from 1,911 cancer census genes. Millions of somatic cancer variants have been identified due to precision medicine and next-generation sequencing (NGS). What is CancerVar? Why Was CancerVar Developed?
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