Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | CP000730 | 1693599 | 1693671 | 73 | 2 [1] | [1] 2 | [hemN] | [hemN] |
AAACCTCATTACCTATGACTTTCCCTCTATTTGTAAGTGCAATCACATCGTTCTTTTCTACAATTAATTCCTTCTCTTTTAAATTATTTATTGTTTGACCAAAGACACTTTCAATAGATTGGTCAAACTTCTTTTTGAACCTACTACTAC > CP000730/1693663‑1693812 | aaaCCTCATTACCTATGACTTTCCCTCTATTTGTAAGTGCAATCACATCGTTCTTTTCTACAATTAATTCCTTCTCTTTTAAATTATTTATTGTTTGACCAAAGACACTTTCAATAGATTGGTCAAACTTCTTTTTGAAcc < 2:45269/141‑1 (MQ=255) tACCTATGACTTTCCCTCTATTTGTAAGTGCAATCACATCGTTCTTTTCTACAATTAATTCCTTCTCTTTTAAATTATTTATTGTTTGACCAAAGACACTTTCAATAGATTGGTCAAACTTCTTTTTGAACCtactactac > 1:2763/1‑141 (MQ=255) | AAACCTCATTACCTATGACTTTCCCTCTATTTGTAAGTGCAATCACATCGTTCTTTTCTACAATTAATTCCTTCTCTTTTAAATTATTTATTGTTTGACCAAAGACACTTTCAATAGATTGGTCAAACTTCTTTTTGAACCTACTACTAC > CP000730/1693663‑1693812 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |