Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 696473–696506 | 696584–696542 | 37–112 | 4 [3] | [3] 5 | [glnX]–[glnV] | [glnX],[glnV] |
TGCCGGAATCAGAATCCGGT‑GCCTTACCGCTTGGCGATACCCCAACAAATTGGTTTTGAAT > NC_000913/696573‑696633 | tGCCGGAATCAGAATCCGGT‑GCCTTACCGCTTGGCGATACCCCAACaaa < 1:634677/49‑1 (MQ=38) cGGAATCAGAATCCGGT‑GCCTTACCGCTTGGCGATACCCCAACAAATTg < 1:1182177/49‑1 (MQ=255) cAGAATCCGGT‑GCCTTACCGCTTGGCGATACCCCAACAAATTGGtttt > 1:510555/1‑48 (MQ=255) aaTCCGGT‑GCCTTACCGCTTGGCGATACCCCAACAAATTGGTTTTGAAt > 1:1873447/1‑49 (MQ=255) aaTCCCGTGGCCTTCCCG‑TTGGCGATACCCCAACAAATTGGTTTTGAAt < 1:1758668/49‑1 (MQ=21) | TGCCGGAATCAGAATCCGGT‑GCCTTACCGCTTGGCGATACCCCAACAAATTGGTTTTGAAT > NC_000913/696573‑696633 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 17 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |