Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_002947 | 2191649 | 2191735 | 87 | 2 [1] | [0] 2 | PP_1937 | helicase |
TCACCTGGCAAGAGGCTTTGGCGAGGGCTTGCGGAGAGCTGCTCGAAAGCGATTGGGCCAAGTCTTATTTGGATTCGTTATTCGAGGCCGATCCGTTAAATCTGTGGCCATCGCAACGCCAAGGCATAGCACAGGC > NC_002947/2191736‑2191871 | tCACCTGGCAAGAGGCTTTGGCGAGGGCTTGCGGAGAGCTGCTCGAAAGCGATTGGGCCAAGTCTTATTTGGATTCGTTATTCGAGGCCGATCCGTTAAATCTGTGGCCATCGCACCGCCAAGGCATAGCACAGgc > 1:437119/1‑136 (MQ=255) tCACCTGGCAAGAGGCTTTGGCGAGGGCTTGCGGAGAGCTGCTCGAAAGCGATTGGGCCAAGTCTTATTTGGATTCGTTATTCGAGGCCGATCCGTTAAATCTGTGGCCATCGCAACGCCAAGGCATAGCACAGgc > 1:165551/1‑136 (MQ=255) | TCACCTGGCAAGAGGCTTTGGCGAGGGCTTGCGGAGAGCTGCTCGAAAGCGATTGGGCCAAGTCTTATTTGGATTCGTTATTCGAGGCCGATCCGTTAAATCTGTGGCCATCGCAACGCCAAGGCATAGCACAGGC > NC_002947/2191736‑2191871 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 21 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |