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.

补充文件1：附表S1。按分子诊断阳性与阴性状态分类的已测序RCHSD病例的临床诊断频次。附表S2：按分子诊断阳性与阴性状态分类的已测序犹他州NeoSeq病例的主要临床诊断。附表S3：RCHSD队列患者的个体MPSE评分。附表S4：犹他州NeoSeq队列患者的个体MPSE评分。