Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | CP000730 | 1290797 | 1290851 | 55 | 2 [1] | [1] 2 | infB | translation initiation factor IF‑2 |
AATAAACCACAAAATCAACCAGCTGCTCCAAAAGAAATACCATCAAAAGTGACATATCAAGAAGGTATTACAGTAGGCGAATTTGCGGATAAATTAAATGTTGAATCATCAGAAATTATCAAAAAATTATTCTTACTTGGTATTGT > CP000730/1290656‑1290801 | aataaACCACAAAATCAACCAGCTGCTCCAAAAGAAATACCATCAAAAGTGACATATCAAGAAGGTATTACAGTAGGCGAATTTGCGGATAAATTAAATGTTGAATCATCAGAAATTATCAAAAAATTATTCTTACTTGGt < 2:43768/141‑1 (MQ=255) aCCAAAAAATCAACCAGCTGCTCCAATAGAAATACCATCAAAAGTGACATATCAAGAAGGTATTACAGTAGGCGAATTTGAGGATAAATTAAATGTTGAATCATAAAAAAAAAAAAAAAAATTATTCTTACTTGGTAttgt < 2:23937/141‑1 (MQ=255) | AATAAACCACAAAATCAACCAGCTGCTCCAAAAGAAATACCATCAAAAGTGACATATCAAGAAGGTATTACAGTAGGCGAATTTGCGGATAAATTAAATGTTGAATCATCAGAAATTATCAAAAAATTATTCTTACTTGGTATTGT > CP000730/1290656‑1290801 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |