Figures & data
Figure 1. Receiver operating characteristic curve for sRNA prediction. Panel A shows the ROC curve for sRNA prediction performance by the PredsRNA program in genic and non-genic category. A total of 1174 sRNA, 5870 genic, and 5870 non-genic non-sRNA sequences were considered to measure the performance. Panel B and C shows the performance of sRNA prediction by PredsRNA and RNAz programs in genic and non-genic categories, respectively. A total of common 334 sRNA, 1670 genic, and 1670 non-genic non-sRNA sequences were considered to measure the performance
![Figure 1. Receiver operating characteristic curve for sRNA prediction. Panel A shows the ROC curve for sRNA prediction performance by the PredsRNA program in genic and non-genic category. A total of 1174 sRNA, 5870 genic, and 5870 non-genic non-sRNA sequences were considered to measure the performance. Panel B and C shows the performance of sRNA prediction by PredsRNA and RNAz programs in genic and non-genic categories, respectively. A total of common 334 sRNA, 1670 genic, and 1670 non-genic non-sRNA sequences were considered to measure the performance](/cms/asset/9280ec40-fa3d-45d9-b685-444afc7afa30/krnb_a_1836455_f0001_oc.jpg)
Figure 2. Prediction of sRNA targets. Panel A demonstrates the sRNA-mRNA target binding region identification protocol (Component I) of PredTAR. The main aim of this protocol is to identify the un-pairing probability of each base from both sRNA and mRNA sequences and utilize this probability information to identify the binding region. Panel B describes the Component II protocol used by PresRAT to identify the sRNA-mRNA target binding region. In this protocol, the energetic value of both sRNA and mRNA secondary structures are taken into account to identify binding regions
![Figure 2. Prediction of sRNA targets. Panel A demonstrates the sRNA-mRNA target binding region identification protocol (Component I) of PredTAR. The main aim of this protocol is to identify the un-pairing probability of each base from both sRNA and mRNA sequences and utilize this probability information to identify the binding region. Panel B describes the Component II protocol used by PresRAT to identify the sRNA-mRNA target binding region. In this protocol, the energetic value of both sRNA and mRNA secondary structures are taken into account to identify binding regions](/cms/asset/1b0fb157-93b1-4391-ae21-fb96b67ab197/krnb_a_1836455_f0002_oc.jpg)
Figure 3. sRNA target finding performance. Panel A shows the frequency distribution of sRNA binding sites in the 91 mRNA sequences. In 98% of the cases, it is found that the sRNA binding site is present within the window of −250 to +100 nucleotides (0 being the translation initiation site) of the target gene. Panel B shows the overlap of correctly predicted target by the PresRAT Component I and II protocols, respectively. Panel C shows the PresRAT sensitivity in predicting the correct sRNA-mRNA target binding regions in 88 samples compared to other programs. Panel D shows the number of true sRNA target gene identification through whole-genome search by PresRAT compared to other existing programs
![Figure 3. sRNA target finding performance. Panel A shows the frequency distribution of sRNA binding sites in the 91 mRNA sequences. In 98% of the cases, it is found that the sRNA binding site is present within the window of −250 to +100 nucleotides (0 being the translation initiation site) of the target gene. Panel B shows the overlap of correctly predicted target by the PresRAT Component I and II protocols, respectively. Panel C shows the PresRAT sensitivity in predicting the correct sRNA-mRNA target binding regions in 88 samples compared to other programs. Panel D shows the number of true sRNA target gene identification through whole-genome search by PresRAT compared to other existing programs](/cms/asset/135ea6f1-e0e4-4689-88d9-f9530833e18b/krnb_a_1836455_f0003_oc.jpg)