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
A1 F1 I2 R1 884 257.2 12958910 96.9% 12557183 93.0

Breseq alignment

BRESEQ :: Evidence
Predicted mutation
evidence seq id position mutation annotation gene description
MC JC NC_000913 4,091,572 3461 bp→GCATGCGGATCCTCTAGAGTCGACATATG [rhaD]rhaB [rhaD], rhaA, rhaB

Missing coverage evidence...
   seq id start end size ←reads reads→ gene description
* * ÷ NC_000913 4091572 4095032 3461 244 [0] [0] 262 [rhaD]–rhaB [rhaD],rhaA,rhaB

New junction evidence
  seq id position reads (cov) reads (cov) score skew freq annotation gene product
* ? NC_000913 = 40915710 (0.000)168 (0.990)
+GCATGCGGATCCTCTAGAGTCGACATATG
86/126 0.3 100% coding (283/825 nt) rhaD rhamnulose‑phosphate aldolase
?NC_000913 4095033 = 0 (0.000)intergenic (‑4/‑284) rhaB/rhaS rhamnulokinase/RhaS

GATK/CNVnator alignment

N/A