Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_002947 | 4209912 | 4210286 | 375 | 2 [0] | [1] 2 | [PP_3692] | [PP_3692] |
CCTGGGGCGGTCGTGATCAGCCTTTGGTCGTGCTTATCGCAAAACTCTTTTTCCTAGCCCTGCCAGCCAACATGATTGT > NC_002947/4209833‑4209911 | ccTGGGGCGGTCGTGATCAGCCTTTGGTCGTGCTTATCGCAAAACTCTTTTTCCTAGCCCTGCCAGCCAACATGATtgt < 1:252667/79‑1 (MQ=255) ccTGGGGCGGTCGTGATCAGCCTTTGGTCGTGCTTATCGCAAAACTCTTTTTCCTAGCCCTGCCAGCCAACATGATtgt > 2:252667/1‑79 (MQ=255) | CCTGGGGCGGTCGTGATCAGCCTTTGGTCGTGCTTATCGCAAAACTCTTTTTCCTAGCCCTGCCAGCCAACATGATTGT > NC_002947/4209833‑4209911 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 15 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |