Results 21 - 40 of 54 are showing below:
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ID | Location | Perfect MFE.* | RefSeq Acc. | strand | Start Position | R_P_ratio# | P value |
Predicted miRNA align pattern | |||||||
14022 | 3' | -52.5 | NC_003521.1 | + | 104831 | 0.71 | 0.901381 |
Target: 5'- aGUGCAGCUGGAucuccucggUGAagGCGUUGUG-GACg -3' miRNA: 3'- -CGUGUCGACCU---------ACU--CGCAGUACuCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 106596 | 0.66 | 0.992701 |
Target: 5'- cGguCGGUgaGGAccgUGAGCaUCGUGGGACg -3' miRNA: 3'- -CguGUCGa-CCU---ACUCGcAGUACUCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 108944 | 0.66 | 0.991643 |
Target: 5'- uGCGCGGCUGucGGUG-GCGUCuAUGAc-- -3' miRNA: 3'- -CGUGUCGAC--CUACuCGCAG-UACUcug -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 116884 | 0.66 | 0.99365 |
Target: 5'- gGCGCGGCUGcGgcGGcGCGcCGgcggGAGACc -3' miRNA: 3'- -CGUGUCGAC-CuaCU-CGCaGUa---CUCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 119593 | 0.66 | 0.992701 |
Target: 5'- cGCugGGCggcGGGUGcAGCGUCucGUGcugcagguGGACg -3' miRNA: 3'- -CGugUCGa--CCUAC-UCGCAG--UAC--------UCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 120398 | 0.69 | 0.953202 |
Target: 5'- gGCACAGa-GGAUGGGUG-CAaaGAGACa -3' miRNA: 3'- -CGUGUCgaCCUACUCGCaGUa-CUCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 122710 | 0.67 | 0.989165 |
Target: 5'- gGCGgGGCUGGA--GGCgGUCGUGgucguGGGCg -3' miRNA: 3'- -CGUgUCGACCUacUCG-CAGUAC-----UCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 124165 | 0.68 | 0.980471 |
Target: 5'- aGCgGCGGCUGGA-GAGCGa---GAGGCc -3' miRNA: 3'- -CG-UGUCGACCUaCUCGCaguaCUCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 124483 | 0.66 | 0.990467 |
Target: 5'- cGgGCGGCUGGucguAGCG-CGUGAGGa -3' miRNA: 3'- -CgUGUCGACCuac-UCGCaGUACUCUg -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 126462 | 0.71 | 0.919437 |
Target: 5'- uGUACAGCaUGGAggccAGCGUCAUGAccGAg -3' miRNA: 3'- -CGUGUCG-ACCUac--UCGCAGUACU--CUg -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 126868 | 0.66 | 0.990467 |
Target: 5'- uCGCGGCaGGccu-GCGUCAgUGAGACg -3' miRNA: 3'- cGUGUCGaCCuacuCGCAGU-ACUCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 128182 | 0.66 | 0.992701 |
Target: 5'- cGUGCAGCaccGGGUGgcacAGCGUCuUGAGcGCg -3' miRNA: 3'- -CGUGUCGa--CCUAC----UCGCAGuACUC-UG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 130013 | 0.66 | 0.991643 |
Target: 5'- cGCGCAacggccGCUGGcuuucAGCGUCAUGgagGGGCa -3' miRNA: 3'- -CGUGU------CGACCuac--UCGCAGUAC---UCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 138719 | 0.71 | 0.907637 |
Target: 5'- gGCGCuGGCUGG-UGGuGCGUCcgGAGGg -3' miRNA: 3'- -CGUG-UCGACCuACU-CGCAGuaCUCUg -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 139936 | 0.66 | 0.994576 |
Target: 5'- gGCACGGCcGGAaggccagcucguccaGGGCGcUCuUGAGGCg -3' miRNA: 3'- -CGUGUCGaCCUa--------------CUCGC-AGuACUCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 141954 | 0.66 | 0.990467 |
Target: 5'- gGCGCccaccuGCUGGGcgacGAGCGUCAgGAGcuGCa -3' miRNA: 3'- -CGUGu-----CGACCUa---CUCGCAGUaCUC--UG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 155616 | 0.68 | 0.972393 |
Target: 5'- gGCGCGGCgccGGGUGAcgcaGUGUCGUacgcgaccgagcaaGGGACg -3' miRNA: 3'- -CGUGUCGa--CCUACU----CGCAGUA--------------CUCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 157041 | 0.68 | 0.967399 |
Target: 5'- gGCGCGGUcGGAgGAGCG-CGgcggGGGGCg -3' miRNA: 3'- -CGUGUCGaCCUaCUCGCaGUa---CUCUG- -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 162243 | 0.74 | 0.800479 |
Target: 5'- gGCGCuGGCgGGGUGGGCGUCAacgGGGGu -3' miRNA: 3'- -CGUG-UCGaCCUACUCGCAGUa--CUCUg -5' |
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14022 | 3' | -52.5 | NC_003521.1 | + | 166222 | 0.69 | 0.957085 |
Target: 5'- uGUACAGCUGGuagaaGAGCGUgAUGccgcccGGCg -3' miRNA: 3'- -CGUGUCGACCua---CUCGCAgUACu-----CUG- -5' |
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Note:
When operating RNAhybrid, the pipeline first calculates the perfect minimum free energy (Perfect mfe *) of a putative miRNA when the entire putative miRNA binds to a perfectly complementary target site, then it calculates the minimum free energy of RNA duplex (mfe of the miRNA/mRNA duplex), abbreviated as Rd_mfe. An alignment for which the Rd_mfe to its correspondent Perfect mfe ratio (R_P_ratio #) is more than 66% is regarded as a positive alignment as described by Krek et al. (21). The P_value is calculated by RNAhybrid.
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