Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_002947 | 20790 | 20800 | 11 | 2 [0] | [1] 2 | PP_0016 | hypothetical protein |
CGCCGACTCGTTGCCAGCTGACGCGGGATTGGCGGCCCTCACCTACGAACAGTTTCACGAGTTGTCATCGCGTCTCGCTGTCAGAAGTT > NC_002947/20701‑20789 | cGCCGACTCGTTGCCAGCTGACGCGGGATTGGCGGCCCTCACCTACGAACAGTTTCACGAGTTGTCATCGCGTCTCGCTGTCAGAAGtt > 1:116741/1‑89 (MQ=255) cGCCGACTCGTTGCCAGCTGACGCGGGATTGGCGGCCCTCACCTACGAACAGTTTCACGAGTTGTCATCGCGTCTCGCTGTCAGAAGtt < 2:116741/89‑1 (MQ=255) | CGCCGACTCGTTGCCAGCTGACGCGGGATTGGCGGCCCTCACCTACGAACAGTTTCACGAGTTGTCATCGCGTCTCGCTGTCAGAAGTT > NC_002947/20701‑20789 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |