Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 3423703–3424234 | 3426803–3424238 | 5–3101 | 7 [2] | [3] 4 | [rrfD]–rrlD | [rrfD],rrlD |
TCACTTCAGAGTTGCGAAAATTTGAGAGACTCACGAACAACTTTCGTTGTT > NC_000913/3426802‑3426852 | tCACTTCAGAGTTGCGAAAATTTGAGAGACTCACGAACAACTTTCgttg > 1:1695522/1‑49 (MQ=38) tCACTTCAGAGTTGCGAAAATTTGAGAGACTCACGAACAACTTTCgttg > 1:2315063/1‑49 (MQ=38) cACTTCAGAGTTGCGAAAATTTGAGAGACTCACGAACAACTTTCgttg < 1:1763275/48‑1 (MQ=38) aCTTCAGAGTTGCGAAAATTTGAGAGACTCACGAACAACTTTCgttgtt < 1:746011/49‑1 (MQ=38) | TCACTTCAGAGTTGCGAAAATTTGAGAGACTCACGAACAACTTTCGTTGTT > NC_000913/3426802‑3426852 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |