Results 1 - 20 of 39 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 | |||||||
10321 | 3' | -62.3 | NC_002687.1 | + | 253502 | 0.66 | 0.837493 |
Target: 5'- uGGGACaCGGUGGuGACCuGUGugcgcuGACCGu -3' miRNA: 3'- gCCCUG-GUCGCC-CUGGuCACc-----CUGGU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 307858 | 0.66 | 0.829956 |
Target: 5'- uGGGACCAcCaGGcCUGGUGGGGCg- -3' miRNA: 3'- gCCCUGGUcGcCCuGGUCACCCUGgu -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 325436 | 0.66 | 0.829956 |
Target: 5'- uGGGACCGGCuuuGGcACUuguggucgAGgagGGGACCAc -3' miRNA: 3'- gCCCUGGUCGc--CC-UGG--------UCa--CCCUGGU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 45767 | 0.67 | 0.790166 |
Target: 5'- gGGGGaaGGCGcGGACCAGgGGGAg-- -3' miRNA: 3'- gCCCUggUCGC-CCUGGUCaCCCUggu -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 173454 | 0.67 | 0.790166 |
Target: 5'- uGGGACUggaGGUGGGACUggaggcgcaAGUGGaGGCgCAa -3' miRNA: 3'- gCCCUGG---UCGCCCUGG---------UCACC-CUG-GU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 309667 | 0.67 | 0.790166 |
Target: 5'- aCGGGACCcccaagcGCGGGGCUuucGGaaucGGACCAc -3' miRNA: 3'- -GCCCUGGu------CGCCCUGG---UCac--CCUGGU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 316019 | 0.67 | 0.78099 |
Target: 5'- uGGuGCCGGUGGGGaCGGUGGGgacgguggugacaGCCAa -3' miRNA: 3'- gCCcUGGUCGCCCUgGUCACCC-------------UGGU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 308423 | 0.67 | 0.776775 |
Target: 5'- cCGGcGACCccGGCGGGGcgggcgcgcccccucCCGGUGaGACCGg -3' miRNA: 3'- -GCC-CUGG--UCGCCCU---------------GGUCACcCUGGU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 172291 | 0.67 | 0.764832 |
Target: 5'- gGGGAaCGGUGGGGgCgggGGUGGGACa- -3' miRNA: 3'- gCCCUgGUCGCCCUgG---UCACCCUGgu -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 33530 | 0.68 | 0.747446 |
Target: 5'- aGGGGCgGGacgccaGGGAUacaAGUGGGuGCCAa -3' miRNA: 3'- gCCCUGgUCg-----CCCUGg--UCACCC-UGGU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 98142 | 0.68 | 0.747446 |
Target: 5'- uGGuGCCAGCGGuGCCAGcGGuGCCAg -3' miRNA: 3'- gCCcUGGUCGCCcUGGUCaCCcUGGU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 86049 | 0.68 | 0.738624 |
Target: 5'- gCGGGGCCAGaCGGG-CCuGUGucACCc -3' miRNA: 3'- -GCCCUGGUC-GCCCuGGuCACccUGGu -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 231619 | 0.68 | 0.729726 |
Target: 5'- uGGGAgUGGUGGGAgUGGUGGGAgUg -3' miRNA: 3'- gCCCUgGUCGCCCUgGUCACCCUgGu -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 57458 | 0.68 | 0.729726 |
Target: 5'- aCGGGuCUAGCgucGGGGCC-GUcGGACCAc -3' miRNA: 3'- -GCCCuGGUCG---CCCUGGuCAcCCUGGU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 263060 | 0.68 | 0.711727 |
Target: 5'- uCGGGAUCGGCGGGuuucacuaaacGCCAcgacccGUGcaGGGCCGc -3' miRNA: 3'- -GCCCUGGUCGCCC-----------UGGU------CAC--CCUGGU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 307627 | 0.68 | 0.710821 |
Target: 5'- uGGGagacgauguacucGCC-GUGGGACCGGUcGGGACa- -3' miRNA: 3'- gCCC-------------UGGuCGCCCUGGUCA-CCCUGgu -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 304147 | 0.68 | 0.702641 |
Target: 5'- cCGGcGACCAaaaugGUGGGGCU-GUGGGugCGc -3' miRNA: 3'- -GCC-CUGGU-----CGCCCUGGuCACCCugGU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 45719 | 0.69 | 0.665872 |
Target: 5'- gGGGAaaGGCGcGGACCAGgGGGAgaagagccCCAa -3' miRNA: 3'- gCCCUggUCGC-CCUGGUCaCCCU--------GGU- -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 296489 | 0.69 | 0.656607 |
Target: 5'- gCGGGACUAaaUGGGAUCAGUGGaGGCa- -3' miRNA: 3'- -GCCCUGGUc-GCCCUGGUCACC-CUGgu -5' |
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10321 | 3' | -62.3 | NC_002687.1 | + | 281794 | 0.7 | 0.628741 |
Target: 5'- uGGGAaCGGCGGGGgCAGgggccgGGGcGCCAg -3' miRNA: 3'- gCCCUgGUCGCCCUgGUCa-----CCC-UGGU- -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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