Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_012967 | 2031681–2031702 | 2054967–2054947 | 23246–23287 | 2 [0] | [1] 2 | [cpsG]–[cpsG] | [cpsG],ECB_RS10255,ECB_RS10260,wbbD,ECB_RS10270,wzy,ECB_RS10280,ECB_RS10285,vioB,vioA,wzx,rfbC,rfbA,rfbD,rfbB,galF,wcaM,wcaL,wcaK,wzxC,wcaJ,[cpsG] |
CGGGGTGCGCCAGTTTGCTGTTGATCTCACCGCTTG > NC_012967/2031645‑2031680 | cGGGGTGCGCCAGTTTGCTGTTGATCTCACCGCTTg > 1:809513/1‑36 (MQ=255) cGGGGTGCGCCAGTTTGCTGTTGATCTCACCGCTTg < 2:117141/36‑1 (MQ=255) | CGGGGTGCGCCAGTTTGCTGTTGATCTCACCGCTTG > NC_012967/2031645‑2031680 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 20 ≤ ATCG/ATCG < 29 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |