Genome Nexus (1) aggregates variant information from sources that are relevant to cancer research and clinical applications, (2) allows high-performance programmatic access to the aggregated data via ...
Standardize tumor classification and variant annotation for reproducible cohort building with COSMIC
Accurate interpretation of cancer genomics depends on standardized disease classification, tumor characterization and variant annotation. In this joint COSMIC and QIAGEN webinar, we show how these ...
Precision medicine company Saphetor has built the world’s largest community and knowledge base for human genome variant identification, annotation, and interpretation. Through its open access platform ...
Precision Medicine Landscape of Genomic Testing for Patients With Cancer in the National Institutes of Health All of Us Database Using Informatics Approaches To better use genetic testing, which is ...
A MAJOR genomic study has uncovered dozens of previously unknown asthma risk variants, using a combination of large-scale ...
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