Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_002947 | 557838 | 557868 | 31 | 2 [0] | [0] 2 | [rpsH] | [rpsH] |
CCGATCTGCCGAAAGTACGTGGCGGTCTGGGCGTGTCTATCGTCTCCACCAACAAAGGTGTGATGACTGATCGCGCTGCGCGCGCTGCCGGTGTCGGCGGC > NC_002947/557737‑557837 | ccGATCTGCCGAAAGTACGTGGCGGTCTGGGCGTGTCTATCGTCTCCACCAACAAAGGTGTGATGACTGATCGCGCTGCGCGCGCTGCCGGTGTCggcggc > 1:3406/1‑101 (MQ=255) ccGATCTGCCGAAAGTACGTGGCGGTCTGGGCGTGTCTATCGTCTCCACCAACAAAGGTGTGATGACTGATCGCGCTGCGCGCGCTGCCGGTGTCggcggc < 2:3406/101‑1 (MQ=255) | CCGATCTGCCGAAAGTACGTGGCGGTCTGGGCGTGTCTATCGTCTCCACCAACAAAGGTGTGATGACTGATCGCGCTGCGCGCGCTGCCGGTGTCGGCGGC > NC_002947/557737‑557837 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |