Results 61 - 80 of 165 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 | |||||||
8985 | 3' | -58.5 | NC_002512.2 | + | 95855 | 0.68 | 0.834159 |
Target: 5'- gGGGGCGG-CGUCcUCCcagggccgcGCGCCGAgGa -3' miRNA: 3'- gCUCCGCCgGCAGaAGG---------UGUGGCUgU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 219433 | 0.68 | 0.826196 |
Target: 5'- gCGGcGGCGGCC-UCcUCCGCGCCcccgugcccGACGg -3' miRNA: 3'- -GCU-CCGCCGGcAGaAGGUGUGG---------CUGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 108195 | 0.66 | 0.884927 |
Target: 5'- -aGGGCGGCCacGUC-UCCuauGCACuCGGCGg -3' miRNA: 3'- gcUCCGCCGG--CAGaAGG---UGUG-GCUGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 217848 | 0.66 | 0.884927 |
Target: 5'- aGAGGCGGCagcggUCUGC-CCGGCGu -3' miRNA: 3'- gCUCCGCCGgcagaAGGUGuGGCUGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 92594 | 0.67 | 0.878246 |
Target: 5'- aGGGGCGGCgGUCccgaggCCGguCgCGACGa -3' miRNA: 3'- gCUCCGCCGgCAGaa----GGUguG-GCUGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 105617 | 0.67 | 0.864292 |
Target: 5'- cCGAGGCaccGGCCGUCgucggucUCCGagacCCGGCc -3' miRNA: 3'- -GCUCCG---CCGGCAGa------AGGUgu--GGCUGu -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 227787 | 0.67 | 0.857029 |
Target: 5'- cCGAGccGCGGCCGUaccgcccgCUcCCGC-CCGGCGu -3' miRNA: 3'- -GCUC--CGCCGGCA--------GAaGGUGuGGCUGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 228105 | 0.67 | 0.852582 |
Target: 5'- gCGAGGaGGgCGUCggCCGCaacgucgugcugggcGCCGACGg -3' miRNA: 3'- -GCUCCgCCgGCAGaaGGUG---------------UGGCUGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 217681 | 0.67 | 0.841957 |
Target: 5'- cCGGGcGCuugGGCUGgcUCUUCCcCGCCGGCGu -3' miRNA: 3'- -GCUC-CG---CCGGC--AGAAGGuGUGGCUGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 116672 | 0.67 | 0.841957 |
Target: 5'- uCGuGGCGGaCCG-CgagCCGCugGCCGACGc -3' miRNA: 3'- -GCuCCGCC-GGCaGaa-GGUG--UGGCUGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 143898 | 0.71 | 0.633611 |
Target: 5'- uCGAGGCuGUCGUCgUCCGagagggcgaacuCGCCGACGa -3' miRNA: 3'- -GCUCCGcCGGCAGaAGGU------------GUGGCUGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 222495 | 0.71 | 0.65306 |
Target: 5'- uGGcGGUGGCCGcCUUCUGCGCCuGGCc -3' miRNA: 3'- gCU-CCGCCGGCaGAAGGUGUGG-CUGu -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 220547 | 0.68 | 0.801376 |
Target: 5'- gCGAgGGCGucacGCCGUCUaCCugGCCGuGCGc -3' miRNA: 3'- -GCU-CCGC----CGGCAGAaGGugUGGC-UGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 166299 | 0.68 | 0.792816 |
Target: 5'- aCGAGGCGGCCGcgUCgcccaaCCugGCCa--- -3' miRNA: 3'- -GCUCCGCCGGC--AGaa----GGugUGGcugu -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 201797 | 0.69 | 0.775311 |
Target: 5'- aCGGGGCGgcgaccucuccGCCGUCUccgCCGCGCCcgggGGCu -3' miRNA: 3'- -GCUCCGC-----------CGGCAGAa--GGUGUGG----CUGu -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 197153 | 0.69 | 0.766381 |
Target: 5'- -aAGGUcgccacGGCCGUCUUCCAC-CCG-CGc -3' miRNA: 3'- gcUCCG------CCGGCAGAAGGUGuGGCuGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 124928 | 0.69 | 0.748205 |
Target: 5'- aCGAGaGacacgaGGCCGgcg-CCGCGCCGACGc -3' miRNA: 3'- -GCUC-Cg-----CCGGCagaaGGUGUGGCUGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 207493 | 0.7 | 0.72027 |
Target: 5'- --cGGCGcCCGUCUccggaUCCGCgACCGACGa -3' miRNA: 3'- gcuCCGCcGGCAGA-----AGGUG-UGGCUGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 220388 | 0.7 | 0.701292 |
Target: 5'- uGGGGcCGGCCGUCgUCUAC-CCGcCGc -3' miRNA: 3'- gCUCC-GCCGGCAGaAGGUGuGGCuGU- -5' |
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8985 | 3' | -58.5 | NC_002512.2 | + | 143741 | 0.7 | 0.701292 |
Target: 5'- gGAGGCGGCCGcggcgucggCUUCCAgGuCCG-CGa -3' miRNA: 3'- gCUCCGCCGGCa--------GAAGGUgU-GGCuGU- -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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