Missing coverage evidence... | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 696467–696506 | 696578–696542 | 37–112 | 6 [5] | [4] 6 | [glnX]–[glnV] | [glnX],[glnV] |
AATGCCGGAATCAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACAAATTGGTT > NC_000913/696571‑696627 | aaTGCCGGAATCAGAATCCGGTGCCTTACCGCTTGGCGATACCCcaaca < 1:478238/49‑1 (MQ=32) tGCCGGAATCAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACaaa < 1:687161/49‑1 (MQ=38) ccGGAATCAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACAAAt < 1:1664743/48‑1 (MQ=40) ggAATCAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACAAATTgg > 1:621946/1‑49 (MQ=255) aaTCAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACAAATTGGtt > 1:1199658/1‑49 (MQ=255) aaTCAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACAAATTGGtt < 1:1207746/49‑1 (MQ=255) | AATGCCGGAATCAGAATCCGGTGCCTTACCGCTTGGCGATACCCCAACAAATTGGTT > NC_000913/696571‑696627 |
Alignment Legend |
---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |