Results 81 - 100 of 232 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 | |||||||
30220 | 3' | -50 | NC_006273.1 | + | 126852 | 0.7 | 0.987527 |
Target: 5'- gCCugCAg---CAGCGgcgUAugUGCGUCg -3' miRNA: 3'- -GGugGUaguaGUCGCa--AUugACGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 127506 | 0.7 | 0.987527 |
Target: 5'- aUCAaCGUCAcCAGCGcgUAGCUGUGCg -3' miRNA: 3'- -GGUgGUAGUaGUCGCa-AUUGACGCGg -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 70694 | 0.69 | 0.991508 |
Target: 5'- aCACCGUUGUacGCGU--GCUGCGaCCg -3' miRNA: 3'- gGUGGUAGUAguCGCAauUGACGC-GG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 41489 | 0.69 | 0.991953 |
Target: 5'- -gGCCGUggaaggauugacaggCGUCGGCGUgaggaUGGCaGCGCCg -3' miRNA: 3'- ggUGGUA---------------GUAGUCGCA-----AUUGaCGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 189888 | 0.69 | 0.992584 |
Target: 5'- aCCGCCGggCAUCGcCGUcGGCUGCGaCg -3' miRNA: 3'- -GGUGGUa-GUAGUcGCAaUUGACGCgG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 233641 | 0.69 | 0.993457 |
Target: 5'- gCCACCGUCGUgccggcccaccgcCGGCGc-AGCUcccguccgaGCGCCg -3' miRNA: 3'- -GGUGGUAGUA-------------GUCGCaaUUGA---------CGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 75926 | 0.69 | 0.993549 |
Target: 5'- gCCAUgGUCAUgGGCGaaGACacgGUGCCu -3' miRNA: 3'- -GGUGgUAGUAgUCGCaaUUGa--CGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 188027 | 0.7 | 0.98416 |
Target: 5'- -uGCUAUCGUCgccgguuucgGGCGaUGACaGCGCCg -3' miRNA: 3'- ggUGGUAGUAG----------UCGCaAUUGaCGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 46796 | 0.7 | 0.98416 |
Target: 5'- aCCGgCGUuaagcccgaggaCAUCAGCGUgcACcuggGCGCCg -3' miRNA: 3'- -GGUgGUA------------GUAGUCGCAauUGa---CGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 227106 | 0.71 | 0.982238 |
Target: 5'- aCCGCCcacggCGGCGUggguaUGCGCCg -3' miRNA: 3'- -GGUGGuaguaGUCGCAauug-ACGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 64977 | 0.71 | 0.972766 |
Target: 5'- gUCACCGUCAaCu-CGUUGGCgcGCGCCg -3' miRNA: 3'- -GGUGGUAGUaGucGCAAUUGa-CGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 162893 | 0.71 | 0.972766 |
Target: 5'- aCCACCAUCAUCAccaccauaacGcCGUgacgGACgugGcCGCCg -3' miRNA: 3'- -GGUGGUAGUAGU----------C-GCAa---UUGa--C-GCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 64520 | 0.71 | 0.972766 |
Target: 5'- cCCGCCGgcucgaCAUCGGUGUcc-CUGcCGCCg -3' miRNA: 3'- -GGUGGUa-----GUAGUCGCAauuGAC-GCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 131256 | 0.71 | 0.972766 |
Target: 5'- aUCGCCgcGUCGggucUCGGCGUgcGC-GCGCCg -3' miRNA: 3'- -GGUGG--UAGU----AGUCGCAauUGaCGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 52817 | 0.71 | 0.977874 |
Target: 5'- cUCACCGUCAauuacgccaugUUGGCGgcgUAACcgGUGCCg -3' miRNA: 3'- -GGUGGUAGU-----------AGUCGCa--AUUGa-CGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 103732 | 0.71 | 0.977874 |
Target: 5'- gCGCCG-CGUCAGCGUcguaAGCcaccacGCGCCg -3' miRNA: 3'- gGUGGUaGUAGUCGCAa---UUGa-----CGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 122045 | 0.71 | 0.980145 |
Target: 5'- aCACCAggAUCAGCGagGGCUG-GCUc -3' miRNA: 3'- gGUGGUagUAGUCGCaaUUGACgCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 77152 | 0.71 | 0.980145 |
Target: 5'- aCCGCCGUCGcCGGCc--GACgcGCGCCc -3' miRNA: 3'- -GGUGGUAGUaGUCGcaaUUGa-CGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 152439 | 0.71 | 0.980145 |
Target: 5'- gCCGCCA-CGUacaAGCGgaugUGcuugccgcgcaGCUGCGCCu -3' miRNA: 3'- -GGUGGUaGUAg--UCGCa---AU-----------UGACGCGG- -5' |
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30220 | 3' | -50 | NC_006273.1 | + | 1802 | 0.69 | 0.993549 |
Target: 5'- gCCGCCAaccugUCGUCAccuuacUGUUGGC-GCGCCa -3' miRNA: 3'- -GGUGGU-----AGUAGUc-----GCAAUUGaCGCGG- -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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