Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | AM260479 | 3950672 | 3950702 | 31 | 2 [0] | [0] 2 | copP2 | putative copper uptake P‑type ATPase |
CTGGCCGTCCACCACGCCGGCAATGCCGCGGCCTGGCAGGGCCTGCACTTCCGTGGCCTGCGGCGC > AM260479/3950703‑3950768 | cTGGCCGTCCACCACGCCGGCAATGCCGCGGCCTGGCAGGGCCTGCACTTCCGTGGCCTgcggcgc > 1:48288/1‑66 (MQ=255) cTGGCCGTCCACCACGCCGGCAATGCCGCGGCCTCGCAGGGCCTGCACTTCCGTGGCCTgcggcgc < 2:48288/66‑1 (MQ=255) | CTGGCCGTCCACCACGCCGGCAATGCCGCGGCCTGGCAGGGCCTGCACTTCCGTGGCCTGCGGCGC > AM260479/3950703‑3950768 |
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 < 27 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |