Results 21 - 40 of 70 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 | |||||||
7849 | 3' | -57.8 | NC_001973.1 | + | 3173 | 0.67 | 0.817853 |
Target: 5'- --aCGAGGcGCuGCGGCUcgugucggaggucgCGGCCGCCg -3' miRNA: 3'- cuaGCUCCuCG-CGUCGGa-------------GCUGGUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 64728 | 0.67 | 0.814451 |
Target: 5'- cGUUGAGGAugGUGC-GCCUCGugCAg- -3' miRNA: 3'- cUAGCUCCU--CGCGuCGGAGCugGUgg -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 109290 | 0.67 | 0.814451 |
Target: 5'- --gCGAGGAcCGCuucguGCCgcacCGACCGCUg -3' miRNA: 3'- cuaGCUCCUcGCGu----CGGa---GCUGGUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 153970 | 0.67 | 0.814451 |
Target: 5'- uGGUCGAGcgcgaguuGAGUcCGGCgCgcgCGACCGCCg -3' miRNA: 3'- -CUAGCUC--------CUCGcGUCG-Ga--GCUGGUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 2312 | 0.67 | 0.814451 |
Target: 5'- --gCGAGGAGUcCAGCUgaagcCGGCgACCg -3' miRNA: 3'- cuaGCUCCUCGcGUCGGa----GCUGgUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 48978 | 0.67 | 0.805834 |
Target: 5'- aAUCGAGGGcaCGC-GUCUCGACCaguggACCa -3' miRNA: 3'- cUAGCUCCUc-GCGuCGGAGCUGG-----UGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 121666 | 0.67 | 0.804964 |
Target: 5'- cGGUcCGAGGucaccugcucgacGGCGCGcGCCaggUCGGCCGCg -3' miRNA: 3'- -CUA-GCUCC-------------UCGCGU-CGG---AGCUGGUGg -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 66399 | 0.67 | 0.797067 |
Target: 5'- uGUCGuGGAGCGUguacacgggcgAGCCgggCGACacgGCCu -3' miRNA: 3'- cUAGCuCCUCGCG-----------UCGGa--GCUGg--UGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 36724 | 0.67 | 0.788155 |
Target: 5'- -cUCGAGcGAGCuGCAcGCCgacgUGGCgGCCg -3' miRNA: 3'- cuAGCUC-CUCG-CGU-CGGa---GCUGgUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 45512 | 0.67 | 0.779109 |
Target: 5'- ----uGGGAGCGCGGCUaCGAgaaCCACUa -3' miRNA: 3'- cuagcUCCUCGCGUCGGaGCU---GGUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 43563 | 0.67 | 0.779109 |
Target: 5'- --cCGAGGGcCGUaucaugauGGCUUUGGCCGCCg -3' miRNA: 3'- cuaGCUCCUcGCG--------UCGGAGCUGGUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 20981 | 0.67 | 0.779109 |
Target: 5'- cAUCGcGGAcGCGCAGCgUC-ACCugCu -3' miRNA: 3'- cUAGCuCCU-CGCGUCGgAGcUGGugG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 25120 | 0.68 | 0.769935 |
Target: 5'- ---aGAGcGGGCGCGGCgaUGGCgCGCCa -3' miRNA: 3'- cuagCUC-CUCGCGUCGgaGCUG-GUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 98639 | 0.68 | 0.769011 |
Target: 5'- --cCGAGGAGCGCgacgugcGGCUgcgCGACgACg -3' miRNA: 3'- cuaGCUCCUCGCG-------UCGGa--GCUGgUGg -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 134479 | 0.68 | 0.767159 |
Target: 5'- aGUCGcGGGcgaucacggccaccAGCGgaaccuugcaGGCCUCGACCGCCu -3' miRNA: 3'- cUAGC-UCC--------------UCGCg---------UCGGAGCUGGUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 83402 | 0.68 | 0.760643 |
Target: 5'- -uUCGAGcGAGCGUucGagUUGGCCACCg -3' miRNA: 3'- cuAGCUC-CUCGCGu-CggAGCUGGUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 26193 | 0.68 | 0.760643 |
Target: 5'- -cUUGGGcuggcaGAGCacGCAGCCUCGGCCGUCg -3' miRNA: 3'- cuAGCUC------CUCG--CGUCGGAGCUGGUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 101987 | 0.68 | 0.760643 |
Target: 5'- aGGUgGAGGuGCGCAacgugugccGCUUCGugCuGCCg -3' miRNA: 3'- -CUAgCUCCuCGCGU---------CGGAGCugG-UGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 40109 | 0.68 | 0.760643 |
Target: 5'- -uUUGucGAGCGCGGUCUgcaCGGCgGCCa -3' miRNA: 3'- cuAGCucCUCGCGUCGGA---GCUGgUGG- -5' |
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7849 | 3' | -57.8 | NC_001973.1 | + | 29860 | 0.68 | 0.741738 |
Target: 5'- -uUCGAGG-GCGUgccccuugAGcCCUCG-CCGCCu -3' miRNA: 3'- cuAGCUCCuCGCG--------UC-GGAGCuGGUGG- -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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