Additional file 1 of Reprogramming of RNA silencing triggered by cucumber mosaic virus infection in Arabidopsis

Additional file 1: Supplementary tables. Table S1. Libraries used in this study. Table S2. miRNA accumulation (RPM) in mock and CMV-infected sRNA libraries. Table S3. 21-nt mRNA-derived sRNA accumulation (RPM) in mock and CMV-infected sRNA libraries. Table S4. 21-nt TE-derived sRNA accumulation (RPM) in mock and CMV-infected sRNA libraries. Table S5. vsiRNA-targeted genes identified by PARE sequencing. Table S6. Primers used in this study.

附加文件1：补充表格。表S1：本研究使用的测序文库。表S2：模拟接种与黄瓜花叶病毒（Cucumber Mosaic Virus, CMV）侵染的小RNA（small RNA, sRNA）文库中，微小RNA（microRNA, miRNA）的丰度（每百万比对读段数，Reads Per Million mapped reads, RPM）。表S3：模拟接种与CMV侵染的sRNA文库中，源自信使RNA（messenger RNA, mRNA）的21nt长度小RNA的丰度（RPM）。表S4：模拟接种与CMV侵染的sRNA文库中，源自转座因子（Transposable Element, TE）的21nt长度小RNA的丰度（RPM）。表S5：经PARE测序（Parallel Analysis of RNA Ends sequencing）鉴定得到的病毒来源小干扰RNA（virus-derived small interfering RNA, vsiRNA）靶向基因。表S6：本研究使用的引物。