New junction evidence | |||||||||||
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seq id | position | reads (cov) | reads (cov) | score | skew | freq | annotation | gene | product | ||
* | ? | NC_002947 | 2870849 = | 52 (0.820) | 4 (0.070) | 4/252 | NT | 8.3% | intergenic (+156/‑374) | PP_2522/PP_2524 | transposase/HD domain‑containing protein |
? | NC_002947 | 2870889 = | 39 (0.650) | intergenic (+196/‑334) | PP_2522/PP_2524 | transposase/HD domain‑containing protein |
ATCAGAAAATGGACAACGCCGGATACCCGCTGGTATGGCAGCCCACGCAGCGCCACGGCCACGTTGGTATACGCGTTCTGACCCGCCAAGGCGACGCCTGATTGCCCCTGAGTTCGCTGATCAGAACACCGACCATCCGATCCGCGAACT‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑ < NC_002947/2870998‑2870849 ‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑gcgaactCAGGGGCAATCAGGCGTCGCCTTGGCGGGTCAGAACGCGTATACCAACGTGGCCGTGGCGCTGCGTGGGCTGCCATACCAGCGGGTATCCGGCGTTGTCCATTTTCTGATATCTCGCACCTGCTGTCAGCAAGGTGCTGTCGGTGATG > NC_002947/2870889‑2871036 ATCAGAAAATGGACAACGCCGGATACCCGCTGGTATGGCAGCCCACGCAGCGCCACGGCCACGTTGGTATACGCGTTCTGACCCGCCAAGGCGACGCCTGATTGCCCCTGAGTTCGCTGATCAGAACACCGACCATCCGATCCGCGAAC > 6:10851/1‑149 TCAGAAAATGGACAACGCCGGATACCCGCTGGTATGGCAGCCCACGCAGCGCCACGGCCACGTTGGTATACGCGTTCTGACCCGCCAAGGCGACGCCTGATTGCCCCTGAGTTCGCTGATCAGAACACCGACCATCCGATCCGCGAACT < 2:355562/149‑1 AAATGGACAACGCCGGATACCCGCTGGTATGGCAGCCCACGCAGCGCCACGGCCACGTTGGTATACGCGTTCTGACCCGCCAAGGCGACGCCTGATTGCCCCTGAGTTCGCTGATCAGAACACCGACCATCCGATCCGC < 7:222091/139‑1 AAATGGACAACGCCGGATACCCGCTGGTATGGCAGCCCACGAAGCGCCACGGCCACGTTGGTATACGCGTTCTGACCCGCCAAGGCGACGCCTGATTGCCCCTGAGTTCGCTGATCAGAACACCGACCAACCGATCCGC > 8:222091/1‑139 CCTGAGTTCGCTGATCAGAACACCGACCATCCGATCCGCGAACTCAGGGGCAATCAGGCGTCGCCTTGGCGGGTCAGAACGCGTATACCAACGTGGCCGTGGCGCTGCGTGGGCTGCCATACCAGCGGGTATCCGGCGTTGTCCATTT > 8:309757/1‑148 CTGAGTTCGCTGATCAGAACACCGACCATCCGATCCGCGAACTCAGGGGCAATCAGGCGTCGCCTTGGCGGGTCAGAACGCGTATACCAACGTGGCCGTGGCGCTGCGTGGGCTGCCATACCAGCGG > 5:288018/1‑127 CTGAGTTCGCTGATCAGAACACCGACCATCCGATCCGCGAACTCAGGGGCAATCAGGCGTCGCCTTGGCGGGTCAGAACGCGTATACCAACGTGGCCGTGGCGCTGCGTGGGCTGCCATACCAGCGG < 6:288018/127‑1 CTGATCAGAACACCGACCATCCGATCCTCGAACTCAGGGGCAATCAGGCGTCGCCTTGGCGGGTCAGAACGCGTATACCAACGTGGCCGTGGCGCTGCGTGGGCTGCCATACCAGCGGGTATCCGGCGTTGTCCATTTTCTGATATCTC < 7:309757/149‑1 GCGAACTCAGGGGCAATCAGGCGTCGCCTTGGCGGGTCAGAACGCGTATACCAACGTGGCCGTGGCGCTGCGTGGGCTGCCATACCAGCGGGTATCCGGCGTTGTCCATTTTCTGATATCTCGCACCTGCTGTCAGCAAGGTGCTGTCG < 2:7294/149‑1 TCAGGGGCAATCAGGCGTCGCCTTGGCGGGTCAGAACGCGTATACCAACGTGGCCGTGGCGCTGCGTGGGCTGCCATACCAGCGGGTATCCGGCGTTGTCCATTTTGTTATATCTCGCACCTGCGGTCAGCGAGGTGCTGTCGGTGATG > 5:322344/1‑149 TCAGGGGCAATCAGGCGTCGCCTTGGCGGGTCAGAACGCGTATACCAACGTGGCCGTGGCGCTGCGTGGGCTGCCATACCAGCGGGTATCCGGCGTTGTCCATTTTCTGATATCTCGCACCTGCTGTCAGCAAGGTGCTGTCGGTGATG > 2:189709/1‑149 TCAGGGGCAATCAGGCGTCGCCTTGGCGGGTCAGAACGCGTATACCAACGTGGCCGTGGCGCTGCGTGGGCTGCCATACCAGCGGGTATCCGGCGTTGTCCATTTTCTGATATCTCGCACCTGCTGTCAGCAAGGTGCTGTCGGTGATG > 4:228239/1‑149 ATCAGAAAATGGACAACGCCGGATACCCGCTGGTATGGCAGCCCACGCAGCGCCACGGCCACGTTGGTATACGCGTTCTGACCCGCCAAGGCGACGCCTGATTGCCCCTGAGTTCGCTGATCAGAACACCGACCATCCGATCCGCGAACT‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑ < NC_002947/2870998‑2870849 ‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑‑gcgaactCAGGGGCAATCAGGCGTCGCCTTGGCGGGTCAGAACGCGTATACCAACGTGGCCGTGGCGCTGCGTGGGCTGCCATACCAGCGGGTATCCGGCGTTGTCCATTTTCTGATATCTCGCACCTGCTGTCAGCAAGGTGCTGTCGGTGATG > NC_002947/2870889‑2871036 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 21 ≤ 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. |