Fig. 8From: De novo sequencing and comparative transcriptome analysis of the male and hermaphroditic flowers provide insights into the regulation of flower formation in andromonoecious Taihangia rupestris Validation of 16 randomly selected differentially expressed genes (DEGs) derived from RNA-seq using Real-time quantitative RT-PCR. Quantitative gene expression data represented as the mean ± SD are shown on the left. The EF1α and UBQ were used as reference genes. Statistically significant differences of relative expression derived from one-way ANOVA at the level of P < 0.05 were marked as different lowercase letters. The normalized FPKM, transformed by log2 (1+ FPKM), were indicated on the rightBack to article page