Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_002947 | 5004754 | 5004917 | 164 | 2 [1] | [0] 2 | PP_4409 | site‑specific recombinase |
GCAGCAACAAATGCGCGCAATTCTGAAGCTGATCAAATACTGTGGCGCGACATAAACTTCACATCACGAGAAGTTTTTCTTGTCAACCCCCAT > NC_002947/5004918‑5005010 | gcagcaACAAATGCGCGCAATTCTGAAGCTGATCAAATACTGTGGCGCGACATAAACTTCACATCACGAGAAGTTTTTCTTGTCAACCCCCAt > 1:163056/1‑93 (MQ=255) gcagcaACAAATGCGCGCAATTCTGAAGCTGATCAAATACTGTGGCGCGACATAAACTTCACATCACGAGAAGTTTTTCTTGTCAACCCCCAt < 2:163056/93‑1 (MQ=255) | GCAGCAACAAATGCGCGCAATTCTGAAGCTGATCAAATACTGTGGCGCGACATAAACTTCACATCACGAGAAGTTTTTCTTGTCAACCCCCAT > NC_002947/5004918‑5005010 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 21 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |