Sample Resequencing Stats

Note: The mutation counts shown below represent unfiltered mutation sets.
ALE, Flask, Isolate Predicted Mutations Mean Coverage Total Reads Percent Mapped Mapped Reads Average Read Length
A5 F26 I1 R1 57 84.6 3443374 98.5% 3391723 147.1

Breseq alignment

BRESEQ :: Evidence
Predicted mutation
evidence seq id position mutation annotation gene description
MC JC NC_002947_CJ‑RC 5,398,630 Δ33,798 bp [hsdM][PP_4768] 28 genes

Missing coverage evidence...
   seq id start end size ←reads reads→ gene description
* * ÷ NC_002947_CJ‑RC 5398630 5432427 33798 61 [0] [0] 62 [hsdM]–[PP_4768] [hsdM],hsdS,PP_5711,PP_4743,PP_4745,PP_4746,PP_4748,PP_4749,PP_4750,PP_4751,PP_4752,stcD,PP_4754,PP_4755,gabP‑V,gudD,PP_4758,PP_4759,PP_4760,PP_4761,tesB,PP_4763,PP_5712,PP_4764,PP_4765,rhlE‑I,yedA,[PP_4768]

New junction evidence
  seq id position reads (cov) reads (cov) score skew freq annotation gene product
* ? NC_002947_CJ‑RC = 53986290 (0.000)61 (0.770) 52/288 0.6 100% coding (40/1218 nt) hsdM type I restriction modification system methylase
?NC_002947_CJ‑RC 5432428 = 0 (0.000)coding (217/612 nt) PP_4768 exonuclease

GATK/CNVnator alignment

N/A