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
A14 F34 I30 R1 12 87.5 2905532 96.3% 2798027 145.0

Breseq alignment

BRESEQ :: Evidence
Predicted mutation
evidence seq id position mutation annotation gene description
MC JC CP009273 3,360,110 Δ10,684 bp IS5‑mediated [yhcE]sspA [yhcE], yhcF, yhcG, yhcH, nanK, nanE, nanT, nanA, nanR, dcuD, sspB, sspA

Missing coverage evidence...
   seq id start end size ←reads reads→ gene description
* * ÷ CP009273 3358981–3360109 3370793 10685–11813 48 [44] [0] 90 insH1–sspA insH1, yhcE, yhcF, yhcG, yhcH, nanK, nanE, nanT, nanA, nanR, dcuD, sspB, sspA

New junction evidence
  seq id position reads (cov) reads (cov) score skew freq annotation gene product
* ? CP009273 = 3360109NA (NA)89 (1.020) 69/288 0.2 100% noncoding (1/1195 nt) IS5 repeat region
?CP009273 3370794 = 0 (0.000)intergenic (‑15/+380) sspA/rpsI stringent starvation protein A, phage P1 late gene activator, RNAP‑associated acid‑resistance protein, inactive glutathione S‑transferase homolog/30S ribosomal subunit protein S9

GATK/CNVnator alignment

N/A