Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | CP000730 | 2382641 | 2382677 | 37 | 2 [1] | [1] 2 | swrC | RND superfamily resistance‑nodulation‑cell division acriflavin:proton (H+) antiporter |
CATCTTTGGCTACTTGAACTGTATTGGCATCTTGAGCTTTAGTTATTTGTAGATTAACCGCATCCTTTCCATTCGTTTTAGAAATAGAAGTACGCACATCACCAACTGTAATATCAGCTAAATCTCCTAGTTTCGCTGTCGGCATACCACTT > CP000730/2382667‑2382818 | cATCTTTGGCTACTTGAACTGTATTGGCATCTTGAGCTTTAGTTATTTGTAGATTAACCGCATCCTTTCCATTCGTTTTAGAAATAGAAGTACGCACATCACCAACTGTAATATCAGCTAAATCTCCTAGTTTCGCTGTCg < 1:48318/141‑1 (MQ=255) aCTTGAACTGTATTGGCATCTTGAGCTTTAGTTATTTGTAGATTAACCGCATCCTTTCCATTCGTTTTAGAAATAGAAGTACGCACATCACCAACTGTAATATCAGCTAAATCTCCTAGTTTCGCTGTCGGCATACCACtt > 1:2247/1‑141 (MQ=255) | CATCTTTGGCTACTTGAACTGTATTGGCATCTTGAGCTTTAGTTATTTGTAGATTAACCGCATCCTTTCCATTCGTTTTAGAAATAGAAGTACGCACATCACCAACTGTAATATCAGCTAAATCTCCTAGTTTCGCTGTCGGCATACCACTT > CP000730/2382667‑2382818 |
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: ‑ |