Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 1800114 | 1800203 | 90 | 2 [1] | [1] 2 | infC | translation initiation factor IF‑3 |
TTGCAAATCGTCTTTCACGCGATTAAGCACTTCCATACCGATTTGCTGGTGCGCCATCTCACGACCGCGGAAACGCAGCGTGATTTTGGCTTTATCACCCTCTTCGAGAAAGCGAATCAGGCTGCGGAGTTTTACCTGATAGTCGCCTTCATC > NC_000913/1800180‑1800332 | ttGCAAATCGTCTTTCACGCGATTAAGCACTTCCATACCGATTTGCTGGTGCGCCCTCTCACGACCGCGGAAACGCAGCGGGATTTTGGCTTTATCACCCCTTTCGAGAAAGCGAACAAGGCTGCgggg > 1:347190/1‑127 (MQ=255) aaGCACTTCCATACCGATTTGCTGGTGCGCCATCTCACGACCGCGGAAACGCAGCGTGATTTTGGCTTTATAACCCTCTTCGAGAAAGCGAATCCGGATGCGGGGTTTTACCTGATGTGCGCCTTCAtt > 1:350622/1‑128 (MQ=255) | TTGCAAATCGTCTTTCACGCGATTAAGCACTTCCATACCGATTTGCTGGTGCGCCATCTCACGACCGCGGAAACGCAGCGTGATTTTGGCTTTATCACCCTCTTCGAGAAAGCGAATCAGGCTGCGGAGTTTTACCTGATAGTCGCCTTCATC > NC_000913/1800180‑1800332 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 8 ≤ ATCG/ATCG < 9 ≤ ATCG/ATCG < 20 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |