Additional file 1 of A large-scale genome and transcriptome sequencing analysis reveals the mutation landscapes induced by high-activity adenine base editors in plants

Additional file 1: Supplementary tables. Table S1, Summary of plants with ABEs. Table S2, Mapping statistics of whole-genome sequencing. Table S3, Summary of sgRNA-dependent on-target and off-target loci. Table S4, Summary of all the homozygous SNVs. Table S5, Summary of all the homozygous indels. Table S6, Summary of genomic SNVs detected through WGS. Table S7, Summary of the overlapping SNVs between each of the plants with whole-genome sequencing. Table S8, Mapping statistics of whole-transcriptome sequencing. Table S9, Summary of all the transcriptomic SNVs. Table S10, Summary of clustered A>G DNA SNVs. Table S11, Primers used to verify DNA SNVs by Sanger sequencing. Table S12, Primers used to verify RNA SNVs by Sanger sequencing.

附加文件1：补充附表。表S1：携带腺嘌呤碱基编辑器（Adenine Base Editor, ABE）的植物汇总表；表S2：全基因组测序（whole-genome sequencing, WGS）比对统计结果；表S3：依赖单引导RNA（single guide RNA, sgRNA）的靶位点与脱靶位点汇总表；表S4：所有纯合单核苷酸变异（single nucleotide variant, SNV）汇总表；表S5：所有纯合插入缺失（insertion-deletion, indel）汇总表；表S6：通过全基因组测序检测到的基因组单核苷酸变异汇总表；表S7：每株接受全基因组测序的植株间重叠单核苷酸变异汇总表；表S8：全转录组测序（whole-transcriptome sequencing, WTS）比对统计结果；表S9：所有转录组单核苷酸变异汇总表；表S10：成簇A>G型DNA单核苷酸变异汇总表；表S11：用于通过桑格（Sanger）测序验证DNA单核苷酸变异的引物；表S12：用于通过桑格测序验证RNA单核苷酸变异的引物。