Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | AM260479 | 1257922 | 1257925 | 4 | 2 [0] | [0] 2 | h16_A1156 | Site‑specific recombinase |
CAGCCAGGAACCTGGCACGGACCGCCGCCACCCCGAGCATGTGCGGCTGCGCTACCTGCTGCAGGTGCTGGAGCGGCATCCCGACTGGGCCGGGC > AM260479/1257926‑1258020 | cAGCCAGGAACCTGGCACGGACCGCCGCCACCCCGAGCATGTGCGGCTGCGCTACCTGCTGCAGGTGCTGGAGCGGCATCCCGACTGGGCCGGGc > 1:599561/1‑95 (MQ=255) cAGCCAGGAACCTGGCACGGACCGCCGCCACCCCGAGCATGTGCGGCTGCGCTACCTGCTGCAGGTGCTGGAGCGGCATCCCGACTGGGCCGGGc < 2:599561/95‑1 (MQ=255) | CAGCCAGGAACCTGGCACGGACCGCCGCCACCCCGAGCATGTGCGGCTGCGCTACCTGCTGCAGGTGCTGGAGCGGCATCCCGACTGGGCCGGGC > AM260479/1257926‑1258020 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |