Results 1 - 20 of 193 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 | |||||||
23776 | 3' | -63.4 | NC_005261.1 | + | 88972 | 0.79 | 0.093732 |
Target: 5'- cUCGGGGGCUaCCUCUGCgacaacuuucUCCCCGGCg -3' miRNA: 3'- -GGCCUCCGG-GGAGGCGau--------AGGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 24864 | 0.79 | 0.098541 |
Target: 5'- -gGGAGGCCCCUCCcacggcCUGUCCCCgcccccuugcccGGCg -3' miRNA: 3'- ggCCUCCGGGGAGGc-----GAUAGGGG------------CCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 15233 | 0.77 | 0.122589 |
Target: 5'- gCCGGcguugAGGCCCCgcucgcagugggCCGCgaucgCCCCGGCg -3' miRNA: 3'- -GGCC-----UCCGGGGa-----------GGCGaua--GGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 640 | 0.77 | 0.129403 |
Target: 5'- gCGGcGGCCgCCagcgCCGC-GUCCCCGGCg -3' miRNA: 3'- gGCCuCCGG-GGa---GGCGaUAGGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 33861 | 0.77 | 0.1359 |
Target: 5'- gCCGGgaGGGCCCCccgCCGCccgCCuCCGGCg -3' miRNA: 3'- -GGCC--UCCGGGGa--GGCGauaGG-GGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 82443 | 0.76 | 0.157226 |
Target: 5'- cCCGGccGGCCCCgcgccgCCGUUGccgcCCCCGGCc -3' miRNA: 3'- -GGCCu-CCGGGGa-----GGCGAUa---GGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 78111 | 0.76 | 0.157606 |
Target: 5'- cCCGGccccGGCCCCaCCGCUcgccacccccgccgCCCCGGCg -3' miRNA: 3'- -GGCCu---CCGGGGaGGCGAua------------GGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 75984 | 0.76 | 0.161062 |
Target: 5'- cCCGGGcgcGGCcgCCCUCgCGCUGgacgCCCUGGCg -3' miRNA: 3'- -GGCCU---CCG--GGGAG-GCGAUa---GGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 72650 | 0.75 | 0.168988 |
Target: 5'- cCUGGGGGCCgCCUCgGgcccCCCCGGCg -3' miRNA: 3'- -GGCCUCCGG-GGAGgCgauaGGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 106029 | 0.75 | 0.185893 |
Target: 5'- aCCGGAGGCaCgCCaCCGCgcUgCCCGGCc -3' miRNA: 3'- -GGCCUCCG-G-GGaGGCGauAgGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 32512 | 0.75 | 0.190346 |
Target: 5'- gCGGGGGgUCCgcgCCGCgcccggCCCCGGCc -3' miRNA: 3'- gGCCUCCgGGGa--GGCGaua---GGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 28198 | 0.74 | 0.199534 |
Target: 5'- gCCGGcGGCCUCgccgCCGCUG-CCgCGGCc -3' miRNA: 3'- -GGCCuCCGGGGa---GGCGAUaGGgGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 35709 | 0.74 | 0.219072 |
Target: 5'- gCCGGGGGCUCggUgGCgg-CCCCGGCc -3' miRNA: 3'- -GGCCUCCGGGgaGgCGauaGGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 15976 | 0.73 | 0.224205 |
Target: 5'- -gGGAGGgCCCgggCCGCUcaCCCgGGCa -3' miRNA: 3'- ggCCUCCgGGGa--GGCGAuaGGGgCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 133676 | 0.73 | 0.228385 |
Target: 5'- uCCGGcgccaacGGCUCgCUCCGCUGggagcugcgcgaCCCCGGCg -3' miRNA: 3'- -GGCCu------CCGGG-GAGGCGAUa-----------GGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 121279 | 0.73 | 0.22944 |
Target: 5'- gCGGccGCCCCggccUCGCUcucguccccGUCCCCGGCu -3' miRNA: 3'- gGCCucCGGGGa---GGCGA---------UAGGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 29271 | 0.73 | 0.245766 |
Target: 5'- gCUGGAGGgCCCgCUGCUGacgccCUCCGGCg -3' miRNA: 3'- -GGCCUCCgGGGaGGCGAUa----GGGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 83057 | 0.73 | 0.245766 |
Target: 5'- -aGGGGGCuCCCUgCGCgccCCCgCGGCg -3' miRNA: 3'- ggCCUCCG-GGGAgGCGauaGGG-GCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 43413 | 0.73 | 0.245766 |
Target: 5'- gCCGGGGGCggCCUCCGC---CgCCGGCg -3' miRNA: 3'- -GGCCUCCGg-GGAGGCGauaGgGGCCG- -5' |
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23776 | 3' | -63.4 | NC_005261.1 | + | 124928 | 0.73 | 0.245766 |
Target: 5'- gCGGAGGCUCCgCCGCgcgcgcugUgCCGGCg -3' miRNA: 3'- gGCCUCCGGGGaGGCGaua-----GgGGCCG- -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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