Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_000913 | 2066222–2066304 | 2080591 | 14288–14370 | 5 [2] | [0] 40 | insH‑6–[yeeA] | insH‑6,yoeA,insD‑3,insC‑3,yoeA,yeeP,isrC,flu,yeeR,yeeS,yeeT,cbeA,cbtA,yeeW,yoeF,yeeX,[yeeA] |
AGTGGGGAAATTCTTCTCGGCTGACTCAGTCATTTCATTTCTTCATGTTTG > NC_000913/2066173‑2066223 | aGTGGGGAAATTCTTCTCGGCTGACTCAGTCATTTCATTTCTTCATGtt > 1:1289277/1‑49 (MQ=38) aGTGGGGAAATTCTTCTCGGCTGACTCAGTCATTTCATTTCTTCATGtt < 1:2306150/49‑1 (MQ=38) aGTGGGGAAATTCTTCTCGGCTGACTCAGTCATTTCATTTCTTCATGtt > 1:478452/1‑49 (MQ=38) gTGGGGAAATTCTTCTCGGCTGACTCAGTCATTTCATTTCTTCATGttt > 1:517762/1‑49 (MQ=35) tGGGGAAATTCTTCTCGGCTGACTCAGTCATTTCATTTCTTCATGTTTg < 1:2767796/49‑1 (MQ=32) | AGTGGGGAAATTCTTCTCGGCTGACTCAGTCATTTCATTTCTTCATGTTTG > NC_000913/2066173‑2066223 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |