Additional file 1: of RNA-seq of eight different poplar clones reveals conserved up-regulation of gene expression in response to insect herbivory

Table S1. Number of RNA-seq reads and percentage of uniquely mapped reads. Table S2. Differential expression results from DESeq2. Table S3. Genes forming the co-expression module shown in Fig. 3. Table S4. PFAM enrichment analysis of the genes forming the co-expression module shown in Fig. 3. Table S5. Most strongly induced genes, defined as having top 10% adjusted p-values and log2 fold-changes. Data for the genes were extracted via the GeneList utility on popgenie.org . Table S6. Illumina adapter sequences for each RNA-seq sample. (XLSX 2557 kb)

表S1。RNA测序（RNA-seq）读段数及唯一比对读段占比。表S2。基于DESeq2的差异表达分析结果。表S3。构成图3所示共表达模块的基因。表S4。图3所示共表达模块基因的PFAM富集分析结果。表S5。最强诱导基因，定义为校正后P值与log₂折叠变化排名均处于前10%的基因，相关基因数据通过popgenie.org网站的GeneList工具提取。表S6。各RNA-seq样本的Illumina接头序列。（XLSX 2557 kb）