Results 1 - 20 of 44 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 | |||||||
11933 | 5' | -62.6 | NC_003278.1 | + | 21627 | 0.66 | 0.24953 |
Target: 5'- gGCCaugcugggCGACC-UGGGCaagAGcGCCGGCg -3' miRNA: 3'- aCGGga------GCUGGuACCCGg--UC-CGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 1308 | 0.67 | 0.202596 |
Target: 5'- aGCCCU-GGCCAcaaGGCCAGGCUu-- -3' miRNA: 3'- aCGGGAgCUGGUac-CCGGUCCGGcug -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 18678 | 0.67 | 0.215811 |
Target: 5'- gGCCaUCGGCC-UGuaaucccuucccgccGGCCcGGCCGGCg -3' miRNA: 3'- aCGGgAGCUGGuAC---------------CCGGuCCGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 2542 | 0.66 | 0.225027 |
Target: 5'- cGCCCa-GGCCAgaucGGCguGGCCGGu -3' miRNA: 3'- aCGGGagCUGGUac--CCGguCCGGCUg -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 20266 | 0.66 | 0.239474 |
Target: 5'- gGCCCUgcucggcaacgcuggCGuCCA-GGGCagcauGGCCGGCa -3' miRNA: 3'- aCGGGA---------------GCuGGUaCCCGgu---CCGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 9854 | 0.66 | 0.24258 |
Target: 5'- gGCCU--GGCC-UGGGCCgagugcgccgcgaAGGUCGACa -3' miRNA: 3'- aCGGGagCUGGuACCCGG-------------UCCGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 6819 | 0.66 | 0.243205 |
Target: 5'- aGCCC-CGGCCAacccGGGCaggugcaaGCCGGCa -3' miRNA: 3'- aCGGGaGCUGGUa---CCCGguc-----CGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 9006 | 0.66 | 0.243205 |
Target: 5'- -aCCCUCGcCCggGcGGCUAuGCCGGCg -3' miRNA: 3'- acGGGAGCuGGuaC-CCGGUcCGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 18967 | 0.66 | 0.24953 |
Target: 5'- aGCCCgaGGCCAccggcaUGGaCCcGGCCGACc -3' miRNA: 3'- aCGGGagCUGGU------ACCcGGuCCGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 2632 | 0.68 | 0.172601 |
Target: 5'- aGCCaucagCG-CC-UGGGCCAGGUCGGu -3' miRNA: 3'- aCGGga---GCuGGuACCCGGUCCGGCUg -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 33892 | 0.69 | 0.159139 |
Target: 5'- cGaCCUCG-CUggGGugacaGCCAGGCCGACa -3' miRNA: 3'- aCgGGAGCuGGuaCC-----CGGUCCGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 12345 | 0.69 | 0.154867 |
Target: 5'- cGCCCUCGcCCGcuUGGcacacauccGCCAGucgaucGCCGACa -3' miRNA: 3'- aCGGGAGCuGGU--ACC---------CGGUC------CGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 8156 | 0.75 | 0.050045 |
Target: 5'- cGCCCUCGcCCGUGuGCCcuGGCUGACc -3' miRNA: 3'- aCGGGAGCuGGUACcCGGu-CCGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 11880 | 0.72 | 0.083863 |
Target: 5'- cUGCCUUgGgcaucGCCGcGGGCCGGcGCCGACc -3' miRNA: 3'- -ACGGGAgC-----UGGUaCCCGGUC-CGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 7806 | 0.7 | 0.11432 |
Target: 5'- gGUCCUCGAggcgaaCCAc-GGCCuGGCCGACc -3' miRNA: 3'- aCGGGAGCU------GGUacCCGGuCCGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 23240 | 0.7 | 0.11432 |
Target: 5'- cGCgCUCG-CCAgGGGCC-GGCCGGa -3' miRNA: 3'- aCGgGAGCuGGUaCCCGGuCCGGCUg -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 3615 | 0.7 | 0.124275 |
Target: 5'- cGCCUUgaagaUGugCGcuUGGGCCuugcuGGCCGACa -3' miRNA: 3'- aCGGGA-----GCugGU--ACCCGGu----CCGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 19959 | 0.69 | 0.135029 |
Target: 5'- gUGCCCagGGCCAguacuuccUGGGCCGcaCCGGCu -3' miRNA: 3'- -ACGGGagCUGGU--------ACCCGGUccGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 22491 | 0.69 | 0.146633 |
Target: 5'- cGCCCUgGACC-UGaccgacaaucgcGGCCucgAGGCCGAUc -3' miRNA: 3'- aCGGGAgCUGGuAC------------CCGG---UCCGGCUG- -5' |
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11933 | 5' | -62.6 | NC_003278.1 | + | 9549 | 0.69 | 0.150699 |
Target: 5'- gGCCCUCGAggccgcccuuucCCGcgagcgccaGGcCCAGGCCGACc -3' miRNA: 3'- aCGGGAGCU------------GGUac-------CC-GGUCCGGCUG- -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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