Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | minE | 153705 | 153712 | 8 | 5 [0] | [0] 5 | [hemL] | [hemL] |
GTTCCTGATTCGTAGAAAAAGTGAATGGCTGCTATTCTA > minE/153713‑153751 | gTTCCTGATTCGTAGAAAAAGTGAATGGCTGCTATTCTa > 1:102036/1‑39 (MQ=255) gTTCCTGATTCGTAGAAAAAGTGAATGGCTGCTATTCTa > 1:176881/1‑39 (MQ=255) gTTCCTGATTCGTAGAAAAAGTGAATGGCTGCTATTCTa > 1:189748/1‑39 (MQ=255) gTTCCTGATTCGTAGAAAAAGTGAATGGCTGCTATTCTa > 1:358301/1‑39 (MQ=255) gTTCCTGATTCGTAGAAAAAGTGAATGGCTGCTATTCTa > 1:93523/1‑39 (MQ=255) | GTTCCTGATTCGTAGAAAAAGTGAATGGCTGCTATTCTA > minE/153713‑153751 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 21 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |