<p>Relative expression levels of genes determined by RNAseq to be differentially expressed <i>in vivo</i> compared to A. <i>in vitro</i> mid-log cultures and B. <i>in vitro</i> stationary phase cultures. Relative expression was assessed using the 2(-Delta Delta C(T)) method, error bars represent standard deviation of three independent biological replicates.</p
<p>Validation of 12 randomly chosen, differentially expressed genes was performed with qPCR using th...
<p>Expression levels of 26 randomly selected genes in the four samples used in this study were detec...
<p>Data from qPCR are shown as means ± standard error (SE) of three replicates. RPKM from RNA-seq ar...
<p>Twenty-five genes that whose expression was significantly different in the control and treatment ...
<p>Expression of eight genes, showing varied expression patterns in RNA-sequencing experiment, were ...
<p>Gene expression differences analyzed by qRT-PCR and RNA-seq are both exhibited. For qRT-PCR, erro...
a<p>RNA for qRT-PCR validation was obtained from independent biological samples.</p>b<p>Differential...
<p>Twenty-two genes were arbitrary selected, from highly up-regulated to highly down-regulated conti...
The grey-scale bars represent relative gene expression in control (dark grey) and treated plants (li...
<p>Eight genes were selected, and their transcript levels were quantified by Q-RT-PCR. Results of Q-...
a<p>Fold difference for each gene was calculated by FPKM value of PHF-DPCs and SHF-DPCs.</p>b<p>Usin...
<p>Note: The validation of the accuracy of RNA-seq data was carried out by comparing of RPKM and the...
<p>Validation of the expression profile between RNA-Seq and RT-qPCR for selected genes.</p
<p>(A) Close correlation (r<sup>2</sup> = 0.80) of 12 selected genes between two approaches. (B) Com...
Five genes were selected to verify RNA-Seq results using qRT-PCR. Graphs on the left (A, C, E, G, I,...
<p>Validation of 12 randomly chosen, differentially expressed genes was performed with qPCR using th...
<p>Expression levels of 26 randomly selected genes in the four samples used in this study were detec...
<p>Data from qPCR are shown as means ± standard error (SE) of three replicates. RPKM from RNA-seq ar...
<p>Twenty-five genes that whose expression was significantly different in the control and treatment ...
<p>Expression of eight genes, showing varied expression patterns in RNA-sequencing experiment, were ...
<p>Gene expression differences analyzed by qRT-PCR and RNA-seq are both exhibited. For qRT-PCR, erro...
a<p>RNA for qRT-PCR validation was obtained from independent biological samples.</p>b<p>Differential...
<p>Twenty-two genes were arbitrary selected, from highly up-regulated to highly down-regulated conti...
The grey-scale bars represent relative gene expression in control (dark grey) and treated plants (li...
<p>Eight genes were selected, and their transcript levels were quantified by Q-RT-PCR. Results of Q-...
a<p>Fold difference for each gene was calculated by FPKM value of PHF-DPCs and SHF-DPCs.</p>b<p>Usin...
<p>Note: The validation of the accuracy of RNA-seq data was carried out by comparing of RPKM and the...
<p>Validation of the expression profile between RNA-Seq and RT-qPCR for selected genes.</p
<p>(A) Close correlation (r<sup>2</sup> = 0.80) of 12 selected genes between two approaches. (B) Com...
Five genes were selected to verify RNA-Seq results using qRT-PCR. Graphs on the left (A, C, E, G, I,...
<p>Validation of 12 randomly chosen, differentially expressed genes was performed with qPCR using th...
<p>Expression levels of 26 randomly selected genes in the four samples used in this study were detec...
<p>Data from qPCR are shown as means ± standard error (SE) of three replicates. RPKM from RNA-seq ar...