Additional file 2: Table S1. of Unraveling the early molecular and physiological mechanisms involved in response to phenanthrene exposure

Transcriptome data obtained for each performed comparison. Table S2. Genes found to be differentially expressed in all the comparisons between PHN-treated and control plants (hybridizations 5–9). Table S3. Genes found to be differentially expressed in all the comparisons between PHN-treated and control plants (hybridizations 5–9), selected after ANOVA analysis. Table S4. The 467 DEGs found to be differentially expressed in all the comparisons between PHN-treated and control plants (hybridizations 5–9), selected after ANOVA analysis. Table S5. Biological pathways with significantly over-represented genes. Table S6. Primers used for quantitative RT-PCR. (XLSX 17507 kb)

本研究针对所有已开展的比较组获取的转录组（transcriptome）数据。
表S2：所有经PHN处理与对照植物的比较组（杂交实验5~9）中鉴定得到的差异表达基因。
表S3：所有经PHN处理与对照植物的比较组（杂交实验5~9）中，经方差分析（ANOVA）筛选得到的差异表达基因。
表S4：经方差分析筛选后，在所有PHN处理与对照植物的比较组（杂交实验5~9）中鉴定得到的467个差异表达基因（DEGs，differentially expressed genes）。
表S5：存在显著富集基因的生物学通路。
表S6：定量实时逆转录聚合酶链式反应（qRT-PCR，quantitative reverse transcription polymerase chain reaction）所用引物。
（XLSX格式，文件大小17507 kb）