Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_002947 | 4210744 | 4210885 | 142 | 2 [0] | [1] 2 | PP_3692 | hypothetical protein |
GCGAACTGAAGCGTGCTATGAGCCAAGTCGCATGAAATTTGTGTCGGCACTCATCGCCACTGCCGATGCCGTCA > NC_002947/4210670‑4210743 | gCGAACTGAAGCGTGCTATGAGCCAAGTCGCATGAAATTTGTGTCGGCACTCATCGCCACTGCCGATGCCGTCa < 1:521924/74‑1 (MQ=255) gCGAACTGAAGCGTGCTATGAGCCAAGTCGCATGAAATTTGTGTCGGCACTCATCGCCACTGCCGATGCCGTCa > 2:521924/1‑74 (MQ=255) | GCGAACTGAAGCGTGCTATGAGCCAAGTCGCATGAAATTTGTGTCGGCACTCATCGCCACTGCCGATGCCGTCA > NC_002947/4210670‑4210743 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |