CancerVar: A New Bioinformatics Tool Developed for Clinical Interpretation of Cancer Mutations
XTalks
MAY 10, 2022
Millions of somatic cancer variants have been identified due to precision medicine and next-generation sequencing (NGS). On Saturday, researchers at the Children’s Hospital of Philadelphia (CHOP) have announced that they developed and launched a new bioinformatics software tool called CancerVar (cancer variant interpretation).
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