Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 3039113 | 3039244 | 132 | 2 [1] | [1] 3 | xerD | site‑specific recombinase |
CAATGACCCGTACCACGCCCTGACGCAGGCTGATATCACTCATTGTCAGTCCGACCAGTTCAGAGACACGCAGCCCGGTAGCATACAACACTTCAAGCAT > NC_000913/3039233‑3039332 | cAATGAGCCGTACCACGCCCTGACGCAGGCTGATATCACTCATTGTCAGTCCGACCAGTTCAGAGACACGc > 1:41194/1‑71 (MQ=255) ccACGCCCTGACGCAGGCTGATATCACTCATTGTCAGTCCGACCAGTTCAGAGACACGCAGCCCGGTAGCATACAACACTTCAAGCAt > 2:13451/1‑88 (MQ=255) ccACGCCCTGACGCAGCCTGATATCACTCATTGTCAGTCCGACCAGTTCAGAGACAAGCAGCCCGGTAGCATACAACACTTCAAGCAt < 1:13451/88‑1 (MQ=255) | CAATGACCCGTACCACGCCCTGACGCAGGCTGATATCACTCATTGTCAGTCCGACCAGTTCAGAGACACGCAGCCCGGTAGCATACAACACTTCAAGCAT > NC_000913/3039233‑3039332 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 16 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |