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. 2019 Dec 3;20:90. doi: 10.1186/s12863-019-0789-x

Fig. 6.

Fig. 6

Comparison between quantitative RT-PCR data and RNA-seq data. Relative expression of the 11 selected ItfWRKYs was analysed by qRT-PCR. The GAPDH transcript levels were used for normalisation. The y-axis represents the relative expression of the fold. Error bars indicate standard deviation. RNA-seq and qRT-PCR data are represented by black and grey bars, respectively