Results 1 - 20 of 75 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 | |||||||
19542 | 5' | -60.8 | NC_004685.1 | + | 39252 | 0.68 | 0.40938 |
Target: 5'- aCGgCGCgaacGGCGUCGGGcaACGCCUCGc -3' miRNA: 3'- gGCgGCG----CCGUAGCUCc-UGCGGAGCu -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 52520 | 0.69 | 0.343587 |
Target: 5'- gCGCCGCGGCGaaCGccGACGCCaUCa- -3' miRNA: 3'- gGCGGCGCCGUa-GCucCUGCGG-AGcu -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 30217 | 0.69 | 0.351382 |
Target: 5'- gCGCCGCGGcCAUCuGGGcGACGCacaagcugUCGGa -3' miRNA: 3'- gGCGGCGCC-GUAG-CUC-CUGCGg-------AGCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 8175 | 0.69 | 0.359301 |
Target: 5'- gCCGCCGCgcacgaggccGGguUCGAGGAgGgCUCc- -3' miRNA: 3'- -GGCGGCG----------CCguAGCUCCUgCgGAGcu -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 50344 | 0.69 | 0.359301 |
Target: 5'- uUCGCCGCGGCGcaucUUGccGAuCGUCUCGGc -3' miRNA: 3'- -GGCGGCGCCGU----AGCucCU-GCGGAGCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 32973 | 0.69 | 0.359301 |
Target: 5'- cCCGCCGUGGCAgcagaUCGAgcagaaGGGCGCaaCGc -3' miRNA: 3'- -GGCGGCGCCGU-----AGCU------CCUGCGgaGCu -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 14560 | 0.69 | 0.367345 |
Target: 5'- aCCGCCGCcacugcuggauuGGCGUCGcAGG-CGaCgUCGAc -3' miRNA: 3'- -GGCGGCG------------CCGUAGC-UCCuGC-GgAGCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 8776 | 0.69 | 0.375511 |
Target: 5'- gCCGUCGUGGC-UUGAGGgcuugaagcucACGCCgCGGu -3' miRNA: 3'- -GGCGGCGCCGuAGCUCC-----------UGCGGaGCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 31486 | 0.69 | 0.383799 |
Target: 5'- cCCGCCGUGGgugcaugcgAUCGAGGACauCUUCGGc -3' miRNA: 3'- -GGCGGCGCCg--------UAGCUCCUGc-GGAGCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 16006 | 0.69 | 0.343587 |
Target: 5'- cCCGCCGUGGCuggucaacGUCGAgcugaagaaGGGCGCgCgccgCGAa -3' miRNA: 3'- -GGCGGCGCCG--------UAGCU---------CCUGCG-Ga---GCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 13380 | 0.7 | 0.335917 |
Target: 5'- cUCGCCuCGGcCAUCGAGGACuGUC-CGGu -3' miRNA: 3'- -GGCGGcGCC-GUAGCUCCUG-CGGaGCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 30836 | 0.7 | 0.328374 |
Target: 5'- -gGCUcaGUGGCAggUCGAGGACGCCaaGGu -3' miRNA: 3'- ggCGG--CGCCGU--AGCUCCUGCGGagCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 14428 | 0.79 | 0.077593 |
Target: 5'- uCCGCCGCgaagcgcucGGCAUCuGGGACGCCagCGAg -3' miRNA: 3'- -GGCGGCG---------CCGUAGcUCCUGCGGa-GCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 9806 | 0.74 | 0.188716 |
Target: 5'- gCCGCCGCGGC---GAGGugGUCcCGGc -3' miRNA: 3'- -GGCGGCGCCGuagCUCCugCGGaGCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 40358 | 0.74 | 0.190624 |
Target: 5'- -gGgCGCGGCAuccggcagaucauccUCGAGGACGCCUgCGc -3' miRNA: 3'- ggCgGCGCCGU---------------AGCUCCUGCGGA-GCu -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 42024 | 0.72 | 0.241693 |
Target: 5'- aCGCUGaCGGCAaCGAGGugGCgCgCGAg -3' miRNA: 3'- gGCGGC-GCCGUaGCUCCugCG-GaGCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 59302 | 0.71 | 0.279093 |
Target: 5'- cCCaCCGCGGCGUCGAuGGcgGCGUCgCGGg -3' miRNA: 3'- -GGcGGCGCCGUAGCU-CC--UGCGGaGCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 43070 | 0.71 | 0.291861 |
Target: 5'- cUCGCCGCGGUcggcugggcgcacAUgUGGGGAUGCC-CGAu -3' miRNA: 3'- -GGCGGCGCCG-------------UA-GCUCCUGCGGaGCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 12652 | 0.7 | 0.299459 |
Target: 5'- gCGCCGCGGCA-CGcGGcCGCUgUCGGa -3' miRNA: 3'- gGCGGCGCCGUaGCuCCuGCGG-AGCU- -5' |
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19542 | 5' | -60.8 | NC_004685.1 | + | 58441 | 0.7 | 0.320956 |
Target: 5'- aC-CCGCGGCGUgcAGGAUGuCCUCGGu -3' miRNA: 3'- gGcGGCGCCGUAgcUCCUGC-GGAGCU- -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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