Results 21 - 40 of 140 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 | |||||||
13969 | 5' | -54.4 | NC_003521.1 | + | 144898 | 0.69 | 0.909396 |
Target: 5'- uGCuGCgGgcccacgGCAUGccggUGGCCGAGGAGUu -3' miRNA: 3'- -CGuCGaCa------CGUGCa---ACUGGCUCCUCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 238696 | 0.77 | 0.563386 |
Target: 5'- gGCGGCcGUGgGaCGUUGACCaGAGGAGg -3' miRNA: 3'- -CGUCGaCACgU-GCAACUGG-CUCCUCg -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 35468 | 0.72 | 0.805826 |
Target: 5'- cGCAGgUcGUGCACGgcGcagcugccgccGCCGAGGAGg -3' miRNA: 3'- -CGUCgA-CACGUGCaaC-----------UGGCUCCUCg -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 100129 | 0.72 | 0.814431 |
Target: 5'- cGCGGCUGgcgGUccuGCGggaaGGCCGuGGGGCu -3' miRNA: 3'- -CGUCGACa--CG---UGCaa--CUGGCuCCUCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 127595 | 0.72 | 0.822876 |
Target: 5'- aGUAGCUGUGCGCGaaGGCCaGuAGGcuGCg -3' miRNA: 3'- -CGUCGACACGUGCaaCUGG-C-UCCu-CG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 137921 | 0.71 | 0.831155 |
Target: 5'- cGUGGCUG-GCGgGUcgcgguucccUGcCCGAGGAGCc -3' miRNA: 3'- -CGUCGACaCGUgCA----------ACuGGCUCCUCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 74632 | 0.71 | 0.847183 |
Target: 5'- aCAGCggggugGUGCGCGg-GACCcuGGAGCg -3' miRNA: 3'- cGUCGa-----CACGUGCaaCUGGcuCCUCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 57285 | 0.71 | 0.847183 |
Target: 5'- aGCAGCaggucgGUGCGCGgcGACUGGuGGAuaaGCg -3' miRNA: 3'- -CGUCGa-----CACGUGCaaCUGGCU-CCU---CG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 148800 | 0.71 | 0.851848 |
Target: 5'- cGCGGCUgcggacguucaucGUGCGCGgcGaccgccugcccucgGCCGAGGuGCg -3' miRNA: 3'- -CGUCGA-------------CACGUGCaaC--------------UGGCUCCuCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 215450 | 0.71 | 0.854919 |
Target: 5'- gGguGCUG-GCGCca-GGCCGAgGGAGCc -3' miRNA: 3'- -CguCGACaCGUGcaaCUGGCU-CCUCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 232569 | 0.71 | 0.862462 |
Target: 5'- gGCuGCUGUGUgg--UGAgCGGGGGGCg -3' miRNA: 3'- -CGuCGACACGugcaACUgGCUCCUCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 137310 | 0.71 | 0.862462 |
Target: 5'- cGCGGCUGcUGCGCGgcGACCcc-GAGUu -3' miRNA: 3'- -CGUCGAC-ACGUGCaaCUGGcucCUCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 60688 | 0.71 | 0.862462 |
Target: 5'- uGCGGCc--GCGCGgggGACCcGGGGGCg -3' miRNA: 3'- -CGUCGacaCGUGCaa-CUGGcUCCUCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 31711 | 0.7 | 0.876941 |
Target: 5'- gGCAGCaUGUGCGCGU--GCUG-GGAcGCc -3' miRNA: 3'- -CGUCG-ACACGUGCAacUGGCuCCU-CG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 151250 | 0.7 | 0.876941 |
Target: 5'- cGCGGcCUG-GgACGgcGACgaCGAGGAGCg -3' miRNA: 3'- -CGUC-GACaCgUGCaaCUG--GCUCCUCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 155297 | 0.7 | 0.88992 |
Target: 5'- cGCGGCUGUuccucucGCAC----GCCGAGGuGCa -3' miRNA: 3'- -CGUCGACA-------CGUGcaacUGGCUCCuCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 120926 | 0.7 | 0.890581 |
Target: 5'- uGCGGCUGccCGCGgcGGCggcuccggCGAGGGGCa -3' miRNA: 3'- -CGUCGACacGUGCaaCUG--------GCUCCUCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 154644 | 0.7 | 0.890581 |
Target: 5'- uCAGCaa-GCACGUgccgcUGGCCGAGGccGGCa -3' miRNA: 3'- cGUCGacaCGUGCA-----ACUGGCUCC--UCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 91525 | 0.69 | 0.909396 |
Target: 5'- -gAGgUGgGCggaGCGUcGACCGGGGAGCc -3' miRNA: 3'- cgUCgACaCG---UGCAaCUGGCUCCUCG- -5' |
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13969 | 5' | -54.4 | NC_003521.1 | + | 121825 | 0.69 | 0.911752 |
Target: 5'- gGUAGUgGUGCACGUUGAugUCGGGcacguucaccaucuuGAGCg -3' miRNA: 3'- -CGUCGaCACGUGCAACU--GGCUC---------------CUCG- -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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