New junction evidence | |||||||||||
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seq id | position | reads (cov) | reads (cov) | score | skew | freq | annotation | gene | product | ||
* | ? | NC_002947 | = 1816168 | 54 (0.950) | 7 (0.130) | 6/250 | NT | 11.0% | coding (40/750 nt) | surE | 5'‑nucleotidase SurE |
? | NC_002947 | = 1816211 | 61 (1.120) | coding (83/750 nt) | surE | 5'‑nucleotidase SurE |
TCCCGAGCCTGATATCCTGCAACTGGAATTCGTCCTGCCGGCCGGATGCTTCGCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCGCAC‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑ > NC_002947/1816018‑1816168 ‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑cgcacTCGGCATAATCCGCCAGCGCAGCGTGCAGCGCGGCGATGCCAGGTGCGGTAACACCGTCGTCATTCGAAATCAGAATACGCATGGGCTGTCCGTCTGCCCTGCCGACACCAGATCCACGACTTCACGCACCACCACGGTGGCGAA < NC_002947/1816211‑1816067 TCCCGAGCCTGATATCCTGCAACTGGAATTCGTCCTGCCGGCCGGATGCTTCGCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCG < 3:206042/148‑1 TCCCGAGCCTGATATCCTGCAACTGGAATTCGTCCTGCCGGCCGGATGCTTCGCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCG > 5:333861/1‑148 CCGAGCCTGATATCCTGCAACTGGAATTCGTCCTGCCGGCCGGATGCTTCGCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCGCAC > 7:79514/1‑149 TGCAACTGGAATTCGTCCTGCCGGCCGGATGCTTCGCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCGCACTCGGCATAATCCGC > 5:203947/1‑148 CTGGAATTCGTCCTGCCGGCCGGATGCTTCGCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCGCACTCGGCATAATCCGCCAGCG > 5:190332/1‑148 TGCTTCGCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCGCACCTGGCAT‑‑‑‑CGCCAGCGCAGCGTGCAGCGCGGCGATGCCAGGTGCG < 4:65913/149‑1 CTTCGCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCGCACTCGGCATAATCCGCCAGCGCAGCGTGCAGCGCGGCGATGCCAGGTG < 6:203947/149‑1 TCGCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCGCACTCGGCATAATCCGCCAGCGCAGCGTGCAGCGCGGCGATGCCAGGTGCG > 1:317548/1‑149 CGCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCGCACTCGGCATAATCCGCCAGCGCAGCGTGCAGCGCGGCGATGCCAGGTGCG < 6:190332/148‑1 GCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCGCACTCGGCATAATCCGCCAGCGCAGCGTGCAGCGCGGCGATGCCAGGTGCGGT < 2:317548/149‑1 GCACTCGGCATAATCCGCCAGCGCAGCGTGCAGCGCGGCGATGCCAGGTGCGGTAACACCGTCGTCATTCGAAATCAGAATACGCATGGGCTGTCCGTCTGCCCTGCCGACACCAGATCCACGACTTCACGCACCACCACGGTGGCGAA < 2:181441/149‑1 TCCCGAGCCTGATATCCTGCAACTGGAATTCGTCCTGCCGGCCGGATGCTTCGCCACCGTGGTGGTGCGTGAAGTCGTGGATCTGGTGTCGGCAGGGCAGACGGACAGCCCATGCGTATTCTGATTTCGAATGACGACGGTGTTACCGCAC‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑ > NC_002947/1816018‑1816168 ‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑cgcacTCGGCATAATCCGCCAGCGCAGCGTGCAGCGCGGCGATGCCAGGTGCGGTAACACCGTCGTCATTCGAAATCAGAATACGCATGGGCTGTCCGTCTGCCCTGCCGACACCAGATCCACGACTTCACGCACCACCACGGTGGCGAA < NC_002947/1816211‑1816067 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |
Reads not counted as support for junction |
read_name Not counted due to insufficient overlap past the breakpoint. |
read_name Not counted due to not crossing MOB target site duplication. |