Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 696473–696506 | 696584–696542 | 37–112 | 4 [3] | [3] 5 | [glnX]–[glnV] | [glnX],[glnV] |
TAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATCAGAATC > NC_000913/696425‑696476 | tAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATCAg > 1:2497639/1‑48 (MQ=255) aaTGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATCAGaa > 1:605806/1‑49 (MQ=40) aTGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATCAGAAt < 1:1093937/49‑1 (MQ=38) tgtgGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATCAGAATc > 1:1334178/1‑49 (MQ=35) | TAATGTGGCTGGGGTACGAGGATTCGAACCTCGGAATGCCGGAATCAGAATC > NC_000913/696425‑696476 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 33 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |