Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 2068563 | 2068598 | 36 | 5 [3] | [2] 4 | yoeH/yoeA | pseudogene, CP4‑44 putative prophage remnant;Phage or Prophage Related/CP4‑44 prophage; putative disrupted hemin or colicin receptor;Phage or Prophage Related; interrupted by IS2 and C‑terminal deletion |
TATCATTACAGTAATCATTTGTACTTTGTATTAATGAGGGATGAAATGTTATATAATATACCTTGTCGA > NC_000913/2068590‑2068658 | tATCATTACAGTAATCATTTGTACTTTGTATTAATGAGGGATGAAATGTTATATAATATACCTTGTCg > 1:510000/1‑68 (MQ=255) aTCATTACAGTAATCATTTGTACTTTGTATTAATGAGGGATGAAATGTTATATAATATACCTTGTCGa > 2:15533/1‑68 (MQ=255) aGTAATCATTTGTACTTTGTATTAATGAGGGATGAAATGt > 1:703893/1‑40 (MQ=255) aGTAATCATTTGTACTTTGTATTAATGAGGGATGAAATGt < 2:703898/40‑1 (MQ=255) | TATCATTACAGTAATCATTTGTACTTTGTATTAATGAGGGATGAAATGTTATATAATATACCTTGTCGA > NC_000913/2068590‑2068658 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |