Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | CP000730 | 1046934 | 1047034 | 101 | 2 [1] | [1] 2 | [menF] | [menF] |
TTGCTGATATTGATTACTCATTGAATACAAAACCTCTTTAAATCATATTTTTTATAACAAAGATATTTTAATAGAAAGTAGCATAAAGGTCAATTGACGTGAAAAATTGCAAGATAAGTTTAAGCAATTCTTGTAACACAATTATCCAAAAATGATACAATATAATAATGAGTGAAAAAAGACGAAGAAAGAAGTGAAA > CP000730/1046793‑1046991 | ttGCTGATATTGATTACTCATTGAATACAAAACCTCTTTAAATCATATTTTTTATAACAAAGATATTTTAATAGAAAGTAGCATAAAGGTCAATTGACGTGAAAAATTGCAAGATAAGTTTAAGCAATTCTTGTAACACaa < 2:15825/141‑1 (MQ=255) aaaGATATTTTAATAGAAAGTAGCATAAAGGTCAATTGACGTGAAAAATTGCAAGATAAGTTTAAGCAATTCTTGTAACACAATTATCCAAAAATGATACAATATAATAATGAGTGAAAAAAGACGAAGAAAGAAGTGaaa > 2:8608/1‑141 (MQ=255) | TTGCTGATATTGATTACTCATTGAATACAAAACCTCTTTAAATCATATTTTTTATAACAAAGATATTTTAATAGAAAGTAGCATAAAGGTCAATTGACGTGAAAAATTGCAAGATAAGTTTAAGCAATTCTTGTAACACAATTATCCAAAAATGATACAATATAATAATGAGTGAAAAAAGACGAAGAAAGAAGTGAAA > CP000730/1046793‑1046991 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |