Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | minE | 1699953 | 1699967 | 15 | 3 [0] | [0] 26 | hcaT | predicted 3‑phenylpropionic transporter |
CAAACGCAGGCCAGAAAGCGCCAGTTCTGGCGAACCAGCGCCAACCACGCAGACC > minE/1699898‑1699952 | caaacGCAGGCCAGAAAGCGCCAGTTCTGGCGAACCAGCGCCAACCACGCAGAcc > 1:1100636/1‑55 (MQ=255) caaacGCAGGCCAGAAAGCGCCAGTTCTGGCGAACCAGCGCCAACCACGCAGAcc > 1:1572317/1‑55 (MQ=255) caaacGCAGGCCAGAAAGCGCCAGTTCTGGCGAACCAGCGCCAACCACGAAGAcc > 1:1006764/1‑55 (MQ=255) | CAAACGCAGGCCAGAAAGCGCCAGTTCTGGCGAACCAGCGCCAACCACGCAGACC > minE/1699898‑1699952 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |