CUSTOM-SEQ: a prototype for oncology rapid learning in a comprehensive EHR environment.
As targeted cancer therapies and molecular profiling become widespread, the era of "precision oncology" is at hand. However, cancer genomes are complex, making mutation-specific outcomes difficult to track. We created a proof-of-principle, CUSTOM-SEQ: Continuously Updating System for Tracking Outcome by Mutation, to Support Evidence-based Querying, to automatically calculate and display mutation-specific survival statistics from electronic health record data.
Author(s): Warner, Jeremy L, Wang, Lucy, Pao, William, Sosman, Jeffrey A, Atreya, Ravi V, Carney, Pam, Levy, Mia A
DOI: 10.1093/jamia/ocw008