Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NZ_CP009273 | 1030569 | 1030582 | 14 | 2 [0] | [1] 3 | hyaC | Ni/Fe‑hydrogenase b‑type cytochrome subunit |
GGTGCGTTAACAGCGAAGGAGAATCATCATGCAACAGAAAAGCGACAACGTTGTCAGCCACTATGTCTTTGAAGC > NZ_CP009273/1030494‑1030568 | ggTGCGTTAACAGCGAAGGAGAATCATCATGCAACAGAAAAGCGACAACGTTGTCAGCCACTATGTCTTTGAAgc < 1:115660/75‑1 (MQ=255) ggTGCGTTAACAGCGAAGGAGAATCATCATGCAACAGAAAAGCGACAACGTTGTCAGCCACTATGTCTTTGAAgc > 2:115660/1‑75 (MQ=255) | GGTGCGTTAACAGCGAAGGAGAATCATCATGCAACAGAAAAGCGACAACGTTGTCAGCCACTATGTCTTTGAAGC > NZ_CP009273/1030494‑1030568 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |