Additional file 1 of Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning

Additional file 1: Table S1. Clinical diagnosis frequencies for sequenced RCHSD cases broken down by positive/negative molecular diagnosis status. Table S2. Primary clinical diagnoses for sequenced Utah NeoSeq cases broken down by positive/negative molecular diagnosis status. Table S3. Individual MPSE scores for RCHSD cohort patients. Table S4. Individual MPSE scores for Utah NeoSeq cohort patients.