Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 1730614 | 1730744 | 131 | 2 [1] | [1] 2 | lhr | putative ATP‑dependent helicase Lhr |
AAACCG‑TTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGCCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGC > NC_000913/1730486‑1730614 | aaaCCC‑TTGCCGCCGGGGCGATGGGTGCATTACAGGTAGCAGAATGGTACTCCCGCGGACGCCGTGCCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCggg < 1:552562/128‑1 (MQ=255) aaCCGTTTGCCCCCG‑GGGGATTGATGCATTAACGGTGAACCGATGGTACCCCCGCGTACGCCGGGCCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGgc < 1:267464/128‑1 (MQ=255) | AAACCG‑TTGCCGCCGCGGCGATGGATGCATTACAGGTAGACGAATGGTACTCCCGCGTACGCCGTGCCGCACCGTGGAAAGATCTGCCAAGACGTGTTTTTGACGCCACGCTGGATATGCTTTCCGGGC > NC_000913/1730486‑1730614 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 8 ≤ ATCG/ATCG < 9 ≤ ATCG/ATCG < 17 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |