Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 1199844 | 1200325 | 482 | 3 [2] | [2] 3 | intE | e14 prophage; putative integrase |
CCAGGAGGTACTTCTCCGTAGTGCTGCGCCTCTTTGAAAACATCAATCAGGACGGAGCGAACTACTTGTGCCATTCTTGGCCGCCCAGCGGCGATATACTCATCAAGCAAT > NC_000913/1200283‑1200393 | ccAGGAGGTACTTCTCCGTAGTGCTGCGCCTCTTTGAAAACATCAATCAGGACGGAGCGAACTACTtg > 1:934704/1‑68 (MQ=255) cgcgcCTCTTTGAAAACATCAATCAGGACGGAGCGAACTACTTGTGCCATTCTTGGCCGCCCAgcggc < 1:753700/67‑1 (MQ=255) caatcaGGACGGAGCGAACTACTAGTGCCATTCTTGGCCGCCCAGCGGCGATATACTCATCAAGCAAt < 2:934708/68‑1 (MQ=255) | CCAGGAGGTACTTCTCCGTAGTGCTGCGCCTCTTTGAAAACATCAATCAGGACGGAGCGAACTACTTGTGCCATTCTTGGCCGCCCAGCGGCGATATACTCATCAAGCAAT > NC_000913/1200283‑1200393 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |