Additional file 2 of Heat-responsive microRNAs participate in regulating the pollen fertility stability of CMS-D2 restorer line under high-temperature stress

Additional file 2: Table S1. Overview of reads from raw data to cleaned sequences in 12 small RNA sequencing (sRNA-seq) libraries. Table S2. Classification statistics of repetitive sequences in total and unique data of 12 sRNA-seq libraries. Table S3. Length distribution of counts of total and unique sRNA sequences in 12 sRNA-seq libraries. Table S4. Detailed summary of identified known and predicted miRNAs and their expression levels in this study. Table S5. Statistics of the number of pre-miRNAs and unique miRNAs in different categories for each sample. Table S6. Length distribution of all identified miRNAs. Table S7. MiFam-based family analysis of identified miRNAs. Table S8. Conservation of the identified miRNAs with other species. Table S9. Conservation profile of the identified miRNA family members. Table S10. The first base preference of mature miRNAs. Table S11. Base preference in different positions of mature miRNAs. Table S12. Identification and expression level analysis of differentially expressed miRNAs. Table S13. Identification and expression level analysis of differentially expressed genes. Table S14. GO functional enrichment analysis of all DEGs. Table S15. KEGG pathway enrichment analysis of all DEGs. Table S16. Overview of degradome sequencing data output for P_NH and P_SH. Table S17. Target gene and predicted cleavage site information validated through degradome sequencing analysis in P_NH and P_SH. Table S18. GO enrichment analysis of the miRNA targets. Table S19. KEGG enrichment analysis of the miRNA targets. Table S20. KEGG enrichment annotation analysis of miRNA targets with negative regulatory relationship under HT stress.