2020
DOI: 10.1200/jco.2020.38.15_suppl.e14074
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Ephesus: A curation workflow tool for the clinical interpretation of genomic variants.

Abstract: e14074 Background: Accurate and comprehensive interpretation of genomic variants has become a bottleneck in clinical sequencing applications due to the accelerated implementation of precision oncology and the rapid growth of relevant biomedical findings. We therefore are motivated to build Ephesus, a framework enabling curation of clinical evidence for biomarkers in somatic cancers. Currently Ephesus is the primary content source for Roche NAVIFY Mutation Profiler (NMP). Methods: Ephesus’ data model ensures a… Show more

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