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
A26 F999 I0 R1 111 30.9 2867207 97.9% 2806995 48.6

Breseq alignment

BRESEQ :: Evidence
Predicted mutation
evidence seq id position mutation annotation gene description
MC JC NC_000913 3,888,432 Δ18,167 bp tnaCbglG 17 genes

Missing coverage evidence...
   seq id start end size ←reads reads→ gene description
* * ÷ NC_000913 3888432 3906598 18167 30 [0] [0] 31 tnaC–bglG tnaC,tnaA,tnaB,mdtL,yidZ,yieE,yieF,adeP,yieH,cbrB,cbrC,yieK,yieL,bglH,bglB,bglF,bglG

New junction evidence
  seq id position reads (cov) reads (cov) score skew freq annotation gene product
* ? NC_000913 = 38884310 (0.000)29 (0.800) 26/94 0.1 100% intergenic (+239/‑4) mnmE/tnaC 5‑carboxymethylaminomethyluridine‑tRNA synthase GTPase subunit/tnaAB operon leader peptide
?NC_000913 3906599 = 0 (0.000)intergenic (‑32/+254) bglG/phoU transcriptional antiterminator BglG/negative regulator of the pho regulon

GATK/CNVnator alignment

N/A