Results 81 - 100 of 118 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 | |||||||
16002 | 5' | -61.5 | NC_004065.1 | + | 150799 | 0.67 | 0.731712 |
Target: 5'- aUCCGCUggUGCgCGAUGUCCaggcucaCCCCg -3' miRNA: 3'- -AGGCGGagACGgGCUGUAGGga-----GGGG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 152631 | 0.71 | 0.488371 |
Target: 5'- aUCC-CCU-UGCCCGACAUCCCgacgCUCg -3' miRNA: 3'- -AGGcGGAgACGGGCUGUAGGGa---GGGg -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 153285 | 0.66 | 0.793558 |
Target: 5'- gCCGCCg--GCgCCG-CG-CCCgUCCCCg -3' miRNA: 3'- aGGCGGagaCG-GGCuGUaGGG-AGGGG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 154370 | 0.69 | 0.589965 |
Target: 5'- gCCGCCUCg--CCGACcUCcacuuccaccuCCUCCCCg -3' miRNA: 3'- aGGCGGAGacgGGCUGuAG-----------GGAGGGG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 155196 | 0.66 | 0.810197 |
Target: 5'- gCCGCCUCgGuCCCGACccgggCgUCUCCa -3' miRNA: 3'- aGGCGGAGaC-GGGCUGuag--GgAGGGG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 157780 | 0.68 | 0.666187 |
Target: 5'- aUCUGCUUCaccagGUCCGACAUCCacaUCUgCg -3' miRNA: 3'- -AGGCGGAGa----CGGGCUGUAGGg--AGGgG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 158056 | 0.68 | 0.675677 |
Target: 5'- gUCGCCUCcgggcUGCCCGGCuccaccggcggcGUCgCCUCCgaCCa -3' miRNA: 3'- aGGCGGAG-----ACGGGCUG------------UAG-GGAGG--GG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 158475 | 0.72 | 0.453428 |
Target: 5'- -gCGCCUCUcCCCGAacaCGUCCgUCCCg -3' miRNA: 3'- agGCGGAGAcGGGCU---GUAGGgAGGGg -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 160237 | 0.69 | 0.608981 |
Target: 5'- cUCCGCCUC-GCUCuGCAUCCUcuUCUUCa -3' miRNA: 3'- -AGGCGGAGaCGGGcUGUAGGG--AGGGG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 160869 | 0.72 | 0.436473 |
Target: 5'- cUCCGCCUCguccaGCgUCGACAg-CUUCCCCa -3' miRNA: 3'- -AGGCGGAGa----CG-GGCUGUagGGAGGGG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 161724 | 0.69 | 0.599463 |
Target: 5'- aCCGUCUCgaaGUCCGuCGccgagCCCUCCUCg -3' miRNA: 3'- aGGCGGAGa--CGGGCuGUa----GGGAGGGG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 163197 | 0.67 | 0.739924 |
Target: 5'- cUCCGCCUCguaCCGgaaaucaacggacGCGUCCCUCggacgUCCg -3' miRNA: 3'- -AGGCGGAGacgGGC-------------UGUAGGGAG-----GGG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 165105 | 0.69 | 0.618514 |
Target: 5'- gUCGUCUCUGaggCGGCGUCCCgCCCg -3' miRNA: 3'- aGGCGGAGACgg-GCUGUAGGGaGGGg -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 165693 | 0.68 | 0.666187 |
Target: 5'- aUCCcaggGCCUCgugugaGCCCGGCuGUCCCUUgaCCa -3' miRNA: 3'- -AGG----CGGAGa-----CGGGCUG-UAGGGAGg-GG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 166989 | 0.67 | 0.722517 |
Target: 5'- gUCGCCUCgcgcGCCgGACAgCUCUCCg- -3' miRNA: 3'- aGGCGGAGa---CGGgCUGUaGGGAGGgg -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 167284 | 0.71 | 0.524527 |
Target: 5'- aUCGCCUCuUGCUgGA-GUCCCUCCUa -3' miRNA: 3'- aGGCGGAG-ACGGgCUgUAGGGAGGGg -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 168801 | 0.68 | 0.675677 |
Target: 5'- cUCCGcCCUCUGCUCcuucgccauCAUcCCCUCgCCg -3' miRNA: 3'- -AGGC-GGAGACGGGcu-------GUA-GGGAGgGG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 169459 | 0.67 | 0.749869 |
Target: 5'- cCCGCCgugugCgGaCCCGGCGUCUCcgucgUCUCCg -3' miRNA: 3'- aGGCGGa----GaC-GGGCUGUAGGG-----AGGGG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 171266 | 0.67 | 0.740832 |
Target: 5'- gUCGCCUCUuuccaaucggGCCCGcCGUCUCUagUCCUg -3' miRNA: 3'- aGGCGGAGA----------CGGGCuGUAGGGA--GGGG- -5' |
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16002 | 5' | -61.5 | NC_004065.1 | + | 171462 | 0.66 | 0.793558 |
Target: 5'- aUCCGCUggaUC-GCgCCGaACAUCCg-CCCCa -3' miRNA: 3'- -AGGCGG---AGaCG-GGC-UGUAGGgaGGGG- -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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