Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 3401559 | 3403360 | 1802 | 2 [1] | [1] 2 | [csrD] | [csrD] |
TAACTCCGATAGTGAGGAAGCGGGCATACTAGCAAATCAGATTTATCTCGCAATTTATTGCGCTTCATCGGCTTTGCTTTTCCATTAGCGAGTATAGTCTTCAGAAATTATTTTCCAATCCATCATGCACATGAGGACCACTTATGCAG > NC_000913/3403341‑3403489 | tAACTCCGATAGTGAGGAAGCGGGCATACTAGCAAATCAGATGTATCTCGCAATTTATTGCGCTTCATCGGCTTTGCTTTGCCATTAGCGATTATAGTCGGCAGAAATTATTTTCCAATCCATCATGCACATGAGGACCACTTATGCAg < 1:265722/149‑1 (MQ=255) cGGGCATACTAGCAAATCAGATTTATCTCGCAATTTATTGCGCTTCATCGGCTTTGCTTTTCCATTAGCGAGTATAGTCTTCAGAAATTATTTTCCAATCCATCATGCACATGAGGACCACTTATGc > 2:163834/1‑127 (MQ=255) | TAACTCCGATAGTGAGGAAGCGGGCATACTAGCAAATCAGATTTATCTCGCAATTTATTGCGCTTCATCGGCTTTGCTTTTCCATTAGCGAGTATAGTCTTCAGAAATTATTTTCCAATCCATCATGCACATGAGGACCACTTATGCAG > NC_000913/3403341‑3403489 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 16 ≤ ATCG/ATCG < 19 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |