Additional file 1 of Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applications

Additional file 1: Table S1. Experimentally validated variants from SpliceVarDB used to train and test Introme. Table S2. Variants experimentally validated using RT-PCR for splice-altering changes by SA Pathology. Table S3. Features in Introme. Table S4. Variants used for allele frequency assessment.

附加文件1：表S1。收录有来自SpliceVarDB的经实验验证的变异体，用于Introme的训练与测试。
表S2。收录有由SA病理研究所（SA Pathology）采用逆转录聚合酶链式反应（Reverse Transcription Polymerase Chain Reaction）对剪接改变变异体进行实验验证得到的变异体。
表S3。收录有Introme所使用的特征。
表S4。收录有用于等位基因频率评估的变异体。