Results 1 - 20 of 187 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 | |||||||
14625 | 3' | -60.2 | NC_003521.1 | + | 124999 | 0.81 | 0.155132 |
Target: 5'- gCCAGCGCcuGCUGAgcCACCCGCgccugagCGGCGg -3' miRNA: 3'- -GGUCGCG--CGACUa-GUGGGCGa------GCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 127308 | 0.71 | 0.600475 |
Target: 5'- cCCAGC-CGCUGcgCACgCuCUCGGUGa -3' miRNA: 3'- -GGUCGcGCGACuaGUGgGcGAGCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 122611 | 0.7 | 0.610038 |
Target: 5'- cCCGGCGacgGCggcGGcCGCgCGCUCGGCGg -3' miRNA: 3'- -GGUCGCg--CGa--CUaGUGgGCGAGCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 197863 | 0.66 | 0.865391 |
Target: 5'- gCCGGCGgGUcg--CGCUCGCUgGGCu -3' miRNA: 3'- -GGUCGCgCGacuaGUGGGCGAgCCGc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 205679 | 0.74 | 0.436675 |
Target: 5'- cCgGGCGCGUgGcgCACCCGCgcucagucgCGGCGa -3' miRNA: 3'- -GgUCGCGCGaCuaGUGGGCGa--------GCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 16744 | 0.73 | 0.462366 |
Target: 5'- gCCGGCGCGCg---CGCCCGC-CGGa- -3' miRNA: 3'- -GGUCGCGCGacuaGUGGGCGaGCCgc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 139309 | 0.72 | 0.506859 |
Target: 5'- gCAGCGCcuGCUGGUCGgCCGCgucUGGCc -3' miRNA: 3'- gGUCGCG--CGACUAGUgGGCGa--GCCGc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 21587 | 0.72 | 0.528859 |
Target: 5'- cCCGGCGCuGCUGAccuggguccugcaacUCugCUGCcUGGCGa -3' miRNA: 3'- -GGUCGCG-CGACU---------------AGugGGCGaGCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 172051 | 0.72 | 0.534415 |
Target: 5'- uCUAGCGCGCUGAggauguucugcgUCAggaCCGUcagCGGCGg -3' miRNA: 3'- -GGUCGCGCGACU------------AGUg--GGCGa--GCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 135224 | 0.71 | 0.590931 |
Target: 5'- gCAGCGC-CUGAgcggcugCGCCgGCggCGGCGa -3' miRNA: 3'- gGUCGCGcGACUa------GUGGgCGa-GCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 155146 | 0.71 | 0.562482 |
Target: 5'- gCGGCGCguGCUGGaCGCCgGCUCGGa- -3' miRNA: 3'- gGUCGCG--CGACUaGUGGgCGAGCCgc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 18172 | 0.72 | 0.534415 |
Target: 5'- gCAGCguggagGCGCUGcgCGCCUGC-CGGCc -3' miRNA: 3'- gGUCG------CGCGACuaGUGGGCGaGCCGc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 16083 | 0.78 | 0.236237 |
Target: 5'- cCCGaCGCGCUGGcCGCCUGCgUCGGCGa -3' miRNA: 3'- -GGUcGCGCGACUaGUGGGCG-AGCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 104107 | 0.71 | 0.566256 |
Target: 5'- gCGGCGCGCUGccaguccucggcggcGUCcugcucgggcccGCCCuGCUCGGUGc -3' miRNA: 3'- gGUCGCGCGAC---------------UAG------------UGGG-CGAGCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 19484 | 0.78 | 0.264358 |
Target: 5'- gCCAG-GUGCaGGUgGCCCGCUCGGUGu -3' miRNA: 3'- -GGUCgCGCGaCUAgUGGGCGAGCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 26758 | 0.72 | 0.531635 |
Target: 5'- gUCGGCGCGCUGGgaccucauguucagUUACCUGUcCGGCc -3' miRNA: 3'- -GGUCGCGCGACU--------------AGUGGGCGaGCCGc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 120833 | 0.71 | 0.57193 |
Target: 5'- gCCAGCgGCGCauGUCGCCCgGCUCGuCGa -3' miRNA: 3'- -GGUCG-CGCGacUAGUGGG-CGAGCcGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 167603 | 0.7 | 0.610038 |
Target: 5'- gCGGCGCGCaGAggCGCCgcaggCGCUCGGgGu -3' miRNA: 3'- gGUCGCGCGaCUa-GUGG-----GCGAGCCgC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 198755 | 0.75 | 0.36485 |
Target: 5'- gCCGuGCuCGCUGGUCGCgCCGCUCgugGGCGa -3' miRNA: 3'- -GGU-CGcGCGACUAGUG-GGCGAG---CCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 27770 | 0.72 | 0.506859 |
Target: 5'- gCCgAGCGCGgaGGaagaaaccuacUCcgGCCCGCUCGGCc -3' miRNA: 3'- -GG-UCGCGCgaCU-----------AG--UGGGCGAGCCGc -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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