Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | REL606 | 2031674–2031721 | 2054972–2054943 | 23223–23299 | 20 [15] | [15] 16 | [manB]–[cpsG] | 23 genes [manB], manC, insB‑14, insA‑14, wbbD, wbbC, wzy, wbbB, wbbA, vioB, vioA, wzx, rmlC, rfbA, rfbD, rfbB, galF, wcaM, wcaL, wcaK, wzxC, wcaJ, [cpsG] |
TCACCGCTTGCCGGAAACGCCGCCATCCGGTCACGTACCAGTTCG > REL606/2054964‑2055008
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tcACCGCTAGCCCGAAACGCCGCCATCCGGCCACGt > 1:4807470/1‑36 (MQ=14)
cccccGTTTGCCGGAAACGCCGCCATCCGGTCACGt < 1:5381560/33‑1 (MQ=14)
cACCGCTTGCCGGAAACGCAGCCATCCGGTCACGTa > 1:5749071/1‑36 (MQ=255)
aCCGCTTGCCGGAAACGCCGCCATCCGGTCACGTAc > 1:1462581/1‑36 (MQ=255)
ccGCTTCCCGGAAACGCCCCCATCCGGTCACGTAcc < 1:4412754/36‑1 (MQ=25)
ccGCTCGCCGAAAACGCCGCCATCCGGTCACGTAcc < 1:3247921/36‑1 (MQ=17)
cGCTTGCCGGAAACGCCGCCATCCGGTCACGTACCa > 1:100870/1‑36 (MQ=255)
gCTTGCCGGAAACGCCGCCATCCGGTCACGTACCAg < 1:642054/36‑1 (MQ=255)
gCTTGCCGGAAACGCCGCCATCCGATCACGAACCAg > 1:6702610/1‑36 (MQ=14)
cTTGCGGAAAACGCCGCCATCCGGTCACGTACCAGt < 1:4280162/36‑1 (MQ=17)
cTTGCCGGAAACGCCGCCATCCGGTCACGTACCAGt > 1:3034769/1‑36 (MQ=255)
cTTGCCGGAAACGCCGCCATCCGGTCACGTACCAGt > 1:4688616/1‑36 (MQ=255)
ttGCCGGAAACGCCGCCATCCGGTCACGTACGAGtt > 1:3150936/1‑36 (MQ=255)
ttGCCGGAAACGCCGCCATCCGGTCACGTACCAGtt < 1:429197/36‑1 (MQ=255)
ttGCCGGAAACGCCGCCATCCGGCCACGTACCAGtt > 1:565482/1‑36 (MQ=255)
gCCGGAAACGCCGCCATCCGGTCACGTACCAGTTCg > 1:4634600/1‑36 (MQ=255)
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TCACCGCTTGCCGGAAACGCCGCCATCCGGTCACGTACCAGTTCG > REL606/2054964‑2055008
Base quality scores: 
ATCG
< 3 ≤
ATCG
< 5 ≤
ATCG
< 10 ≤
ATCG
< 26 ≤
ATCG
< 32 ≤
ATCG
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