Results 61 - 80 of 217 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 | |||||||
29042 | 3' | -56.7 | NC_006146.1 | + | 130511 | 0.66 | 0.872535 |
Target: 5'- aGGUcuagGguGCUGuCAGCAGCCacaauCCGGGCa -3' miRNA: 3'- cUCAa---CguCGGU-GUUGUCGG-----GGUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 130477 | 0.7 | 0.672007 |
Target: 5'- ----cGgGGCCGCuGCcGCCCCGGGUg -3' miRNA: 3'- cucaaCgUCGGUGuUGuCGGGGUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 129542 | 0.66 | 0.865099 |
Target: 5'- aGAGccaCGGCCACcACcgccaGGCCCUGGGCc -3' miRNA: 3'- -CUCaacGUCGGUGuUG-----UCGGGGUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 129348 | 0.66 | 0.857452 |
Target: 5'- -cGgaGCGGCCGguucucgAGCAGCCUCAGGa -3' miRNA: 3'- cuCaaCGUCGGUg------UUGUCGGGGUCCg -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 128531 | 0.66 | 0.872535 |
Target: 5'- -cGUUGCGGCuCACGACcGCCacgaagacguCCcGGCu -3' miRNA: 3'- cuCAACGUCG-GUGUUGuCGG----------GGuCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 128274 | 0.74 | 0.443824 |
Target: 5'- uGAGgcccaCGGCgGCGGCcgAGCCCCAGGCu -3' miRNA: 3'- -CUCaac--GUCGgUGUUG--UCGGGGUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 128215 | 0.67 | 0.816279 |
Target: 5'- gGGGgcucUGcCAGCCucaGGCAGCCCaccgCGGGCg -3' miRNA: 3'- -CUCa---AC-GUCGGug-UUGUCGGG----GUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 128186 | 0.69 | 0.742126 |
Target: 5'- cGGGagGCGGCC-CAggggggcgccGCGGCgCCGGGCc -3' miRNA: 3'- -CUCaaCGUCGGuGU----------UGUCGgGGUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 127515 | 0.67 | 0.807509 |
Target: 5'- cGGGgcagagGCAGCCGCuGCuGCCCCc-GCu -3' miRNA: 3'- -CUCaa----CGUCGGUGuUGuCGGGGucCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 127443 | 0.74 | 0.416988 |
Target: 5'- cGAGgagGCuGCCGCuccagauguGGCGGCCCgCAGGCu -3' miRNA: 3'- -CUCaa-CGuCGGUG---------UUGUCGGG-GUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 125358 | 0.68 | 0.751831 |
Target: 5'- gGAGgccaggGCGGCCAagcccaAGgAGgCCCAGGCc -3' miRNA: 3'- -CUCaa----CGUCGGUg-----UUgUCgGGGUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 123499 | 0.71 | 0.57985 |
Target: 5'- uGAGgcugGCccuGGCCACGGuCGaCCCCAGGCg -3' miRNA: 3'- -CUCaa--CG---UCGGUGUU-GUcGGGGUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 123264 | 0.71 | 0.631017 |
Target: 5'- cGGGccGCGGCCAgaGACGGCUCguGGCc -3' miRNA: 3'- -CUCaaCGUCGGUg-UUGUCGGGguCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 123170 | 0.68 | 0.798578 |
Target: 5'- cGAGga--GGCCccggACGACgAGCUCCGGGCg -3' miRNA: 3'- -CUCaacgUCGG----UGUUG-UCGGGGUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 122837 | 0.67 | 0.816279 |
Target: 5'- cGAGUacGUGGaCCGCAcGCuGCCCgGGGCg -3' miRNA: 3'- -CUCAa-CGUC-GGUGU-UGuCGGGgUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 121156 | 0.69 | 0.702434 |
Target: 5'- cGAGcUGCucuaCCugGGCAccGCCCUAGGCg -3' miRNA: 3'- -CUCaACGuc--GGugUUGU--CGGGGUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 120006 | 0.69 | 0.702434 |
Target: 5'- gGAGgcccaGGCCGCAcccGCGGCCaguCCGGGCa -3' miRNA: 3'- -CUCaacg-UCGGUGU---UGUCGG---GGUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 118063 | 0.7 | 0.692339 |
Target: 5'- cGGggGCGGCgGCGGCucGGCCCUccgcauccuGGGCa -3' miRNA: 3'- cUCaaCGUCGgUGUUG--UCGGGG---------UCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 117875 | 0.7 | 0.651543 |
Target: 5'- cGGcgGCGGCCGCGGCcagccgcgugaGGCCCaGGGCc -3' miRNA: 3'- cUCaaCGUCGGUGUUG-----------UCGGGgUCCG- -5' |
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29042 | 3' | -56.7 | NC_006146.1 | + | 117205 | 0.67 | 0.833308 |
Target: 5'- aGAGgugGCAGUCuCAaacuGCuGcCCCCGGGCu -3' miRNA: 3'- -CUCaa-CGUCGGuGU----UGuC-GGGGUCCG- -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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