A comprehensive atlas of pig RNA editome across 23 tissues reveals RNA editing affecting interaction mRNA-miRNAs

Figure S1: PCA analysis of all tissues. Figure S2: wild(CFLAR-A) and experimental(CFLAR-G) plasmid by PCR and Sanger sequencing. Figure S3: Validation of RNA editing by PCR and Sanger sequencing. Table S1: Information of all samples. Table S2: The filtering criteria for sites of all tissues. Table S3: Primer information for RNA editing validation. Table S4: Primer information of vector construction. Table S5: Information of all RNA editing sites. Table S6: Information of all RNA-seq expression data. Table S7: Specificity of A-to-I editing sites in skeletal muscle of pigs. Table S8: Specificity of A-to-I editing sites of skeletal muscle with GO annotation. Table S9: The result of the prediction of miRNA target regions by miranda software.补充图S1：所有组织的主成分分析（Principal Component Analysis，PCA）。 补充图S2：野生型（CFLAR-A）与实验型（CFLAR-G）质粒的聚合酶链式反应（Polymerase Chain Reaction，PCR）及桑格测序（Sanger Sequencing）结果。 补充图S3：基于聚合酶链式反应与桑格测序的RNA编辑（RNA editing）验证结果。 补充表S1：所有样本的信息。 补充表S2：所有组织的位点筛选标准。 补充表S3：RNA编辑验证所用引物信息。 补充表S4：载体构建所用引物信息。 补充表S5：所有RNA编辑位点的信息。 补充表S6：所有RNA测序（RNA-seq）表达数据的信息。 补充表S7：猪骨骼肌中A-to-I RNA编辑位点的特异性分析结果。 补充表S8：带有基因本体（Gene Ontology，GO）注释的骨骼肌A-to-I RNA编辑位点特异性分析结果。 补充表S9：通过Miranda软件预测的微小RNA（microRNA，miRNA）靶区域结果。