Results 21 - 40 of 47 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 | |||||||
19246 | 5' | -54.4 | NC_004684.1 | + | 24106 | 0.66 | 0.787626 |
Target: 5'- uCGC-GCGGcAUcGCCAAGGACgUGGUGc -3' miRNA: 3'- -GCGuUGCUcUAcCGGUUCCUG-ACCAC- -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 24898 | 0.66 | 0.79735 |
Target: 5'- gGCuACGAGAUGGCCGccgccgcgaucAGcGcGCUGGg- -3' miRNA: 3'- gCGuUGCUCUACCGGU-----------UC-C-UGACCac -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 25054 | 0.75 | 0.309684 |
Target: 5'- gGCGAUGuAGGUGGCCAGGGcgGCcggguUGGUGg -3' miRNA: 3'- gCGUUGC-UCUACCGGUUCC--UG-----ACCAC- -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 25959 | 0.66 | 0.787626 |
Target: 5'- aCGC--CGAGcUGGCCAA--GCUGGUGc -3' miRNA: 3'- -GCGuuGCUCuACCGGUUccUGACCAC- -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 28008 | 0.69 | 0.628752 |
Target: 5'- aCGCggUGAucgGGCCGuacaAGGGCUGGUu -3' miRNA: 3'- -GCGuuGCUcuaCCGGU----UCCUGACCAc -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 29389 | 0.67 | 0.736818 |
Target: 5'- gGC-ACcAGAUGGCCGAGGACaaGGc- -3' miRNA: 3'- gCGuUGcUCUACCGGUUCCUGa-CCac -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 29425 | 0.68 | 0.717813 |
Target: 5'- gGCAACGAuggccuccaggacGAUGGCCuccaccgcgucgagcAGGGcgugcauGCUGGUGa -3' miRNA: 3'- gCGUUGCU-------------CUACCGG---------------UUCC-------UGACCAC- -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 34430 | 0.66 | 0.777741 |
Target: 5'- gGCGGCGAGGuUGGCCAgcgcgAGcGcCUGGa- -3' miRNA: 3'- gCGUUGCUCU-ACCGGU-----UC-CuGACCac -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 39005 | 0.66 | 0.787626 |
Target: 5'- aCGCGuacgGCGAGAggaUGGCCAgcucccAGGACacccGGUa -3' miRNA: 3'- -GCGU----UGCUCU---ACCGGU------UCCUGa---CCAc -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 42186 | 0.72 | 0.459408 |
Target: 5'- gCGCggUGAGcagugGGCCGuGGAgCUGGUGg -3' miRNA: 3'- -GCGuuGCUCua---CCGGUuCCU-GACCAC- -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 42412 | 0.68 | 0.694222 |
Target: 5'- aCGCGcCGAcGcgGGCCAagguaugggcAGGACUGGc- -3' miRNA: 3'- -GCGUuGCU-CuaCCGGU----------UCCUGACCac -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 43821 | 0.66 | 0.806903 |
Target: 5'- gCGCAGCGAGGUcGCCAGGuACUcGUc -3' miRNA: 3'- -GCGUUGCUCUAcCGGUUCcUGAcCAc -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 43850 | 0.67 | 0.736817 |
Target: 5'- cCGCGACc-GAUGccGCCGAGGuuggugagcagGCUGGUGa -3' miRNA: 3'- -GCGUUGcuCUAC--CGGUUCC-----------UGACCAC- -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 48961 | 0.72 | 0.469374 |
Target: 5'- gGCgGGCGGGGUGGCCGGGGcgggcGCgucGGUGc -3' miRNA: 3'- gCG-UUGCUCUACCGGUUCC-----UGa--CCAC- -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 49540 | 0.68 | 0.694222 |
Target: 5'- gGCGguguGCGcGGUGGCCGAcuucGGGCUGGc- -3' miRNA: 3'- gCGU----UGCuCUACCGGUU----CCUGACCac -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 51585 | 0.7 | 0.595919 |
Target: 5'- gGCGGCGAccgGGUGGuCCAAGGuCUccaGGUGu -3' miRNA: 3'- gCGUUGCU---CUACC-GGUUCCuGA---CCAC- -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 51969 | 0.68 | 0.694222 |
Target: 5'- aGCAGCaGGGUGGCCAcGGugUcGGc- -3' miRNA: 3'- gCGUUGcUCUACCGGUuCCugA-CCac -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 54268 | 0.66 | 0.787626 |
Target: 5'- uGCGugGAGAagcugccgcgcUGGCCGguGGGGCgGcGUGc -3' miRNA: 3'- gCGUugCUCU-----------ACCGGU--UCCUGaC-CAC- -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 55083 | 0.68 | 0.672522 |
Target: 5'- aCGCugUGGGAacaGGCCAAGGAgCcGGUGc -3' miRNA: 3'- -GCGuuGCUCUa--CCGGUUCCU-GaCCAC- -5' |
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19246 | 5' | -54.4 | NC_004684.1 | + | 55249 | 0.73 | 0.42072 |
Target: 5'- uGCGG-GAGAUGGaaGAGGAgCUGGUGg -3' miRNA: 3'- gCGUUgCUCUACCggUUCCU-GACCAC- -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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