Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 3315203 | 3315232 | 30 | 2 [1] | [1] 2 | infB | translation initiation factor IF‑2 |
ACGCGCTGCTTTCGCGTTACG‑ACCACGGCCACGGCCGCCTTCGACTTCACGATCGCTTTCGTCTTCTGCCTGGCGAGCATGTTGAGAAGTAGTGACGTGATAATCGCTGGAATCTTCAGTCGGTTCCG > NC_000913/3315232‑3315359 | gcgcgCTTCTTTCCCGTTTCGCCCCCCGGCCA‑GGGCGCCTTCCGCTTTACGATCCCTTTCGGCTTCTGCCTGGCGAGCATGTTGAGAAGTAGTGACGTGATAATCGCTGGAATCTTCAGTCGGTTCcg < 1:348589/127‑1 (MQ=255) aCGCGCTGCTTTCGCGTTACG‑ACCACGGCCACGGCCGCCTTCGACTTCACGATCGCTTTCGTCTTCTGCCTGGCGAGCATGTTGAGAAGTATTGACTTGTAAATGGCTGGAATCTTCAGTGGGTTcc > 1:386917/1‑127 (MQ=255) | ACGCGCTGCTTTCGCGTTACG‑ACCACGGCCACGGCCGCCTTCGACTTCACGATCGCTTTCGTCTTCTGCCTGGCGAGCATGTTGAGAAGTAGTGACGTGATAATCGCTGGAATCTTCAGTCGGTTCCG > NC_000913/3315232‑3315359 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 7 ≤ ATCG/ATCG < 8 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |