Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | minE | 1699907 | 1699921 | 15 | 22 [0] | [1] 2 | hcaT | predicted 3‑phenylpropionic transporter |
CGCCAGTTCTGGCGAACCAGCGCCAACCACGCAGACCAACCGGTGCTCTCCTGCTGGCGACTTGCCCCTTGTG > minE/1699916‑1699988 | cgcCAGTTCTGGCGAACCAGCGCCAACCACGCAGACCAACCGGTGCTCTCCTGCTGGCGACTTGccc > 1:1558044/1‑67 (MQ=255) ttCTGGCGAACCAGCGCCAACCACGCAGACCAACCGGTGCTCTCCTGCTGGCGACTTGCCCCTtgtg > 1:2046253/1‑67 (MQ=255) | CGCCAGTTCTGGCGAACCAGCGCCAACCACGCAGACCAACCGGTGCTCTCCTGCTGGCGACTTGCCCCTTGTG > minE/1699916‑1699988 |
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: ‑ |