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
A4 F111 I0 R1 46 91.4 1555988 99.0% 1540428 264.6

Breseq alignment

BRESEQ :: Evidence
Predicted mutation
evidence seq id position mutation freq annotation gene description
MC JC NC_000913 1,411,925 Δ23,060 bp 100% [ttcA][ttcC] 33 genes

Missing coverage evidence...
   seq id start end size ←reads reads→ gene description
* * ÷ NC_000913 1411925 1434984 23060 82 [0] [0] 82 [ttcA]–[ttcC] 33 genes
[ttcA], intR, ydaQ, ydaC, ralR, recT, recE, racC, ydaE, kilR, sieB, ydaF, ydaG, racR, ydaS, ydaT, ydaU, ydaV, ydaW, rzpR, rzoR, trkG, ynaK, ydaY, tmpR, lomR, insH1, lomR, stfR, tfaR, pinR, ynaE, [ttcC]

New junction evidence
  seq id position reads (cov) reads (cov) score skew freq annotation gene product
* ? NC_000913 = 14119240 (0.000)71 (0.940) 52/456 NT 100% coding (25/936 nt) ttcA tRNA s(2)C32 thioltransferase, iron sulfur cluster protein
?NC_000913 1434985 = 0 (0.000)pseudogene (24/51 nt) ttcC pseudogene, prophage Rac integration site ttcA duplication,Phage or Prophage Related

GATK/CNVnator alignment

N/A