breseq  version 0.33.1  revision 8505477f25b3
mutation predictions | marginal predictions | summary statistics | genome diff | command line log

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsERR2001766.good.fq8,321,009412,706,281100.0%49.6 bases50 bases96.7%
total8,321,009412,706,281100.0%49.6 bases50 bases96.7%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0009134,641,652109.19.4100.0%Escherichia coli str. K-12 substr. MG1655, complete genome.
total4,641,652100.0%

fit dispersion is the ratio of the variance to the mean for the negative binomial fit. It is =1 for Poisson and >1 for over-dispersed data.

New Junction Evidence

Junction Candidates Tested

optionlimitactual
Number of alignment pairs examined for constructing junction candidates≤ 1000005528
Coverage evenness (position-hash) score of junction candidates≥ 2≥ 2
Test this many junction candidates (n). May be smaller if not enough passed the coverage evenness threshold100 ≤ n ≤ 5000124
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.003

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0009130.54672

pr(no read start) is the probability that there will not be an aligned read whose first base matches a given position on a given strand.

Final Junction Predictions

optionvalue
Coverage evenness (position-hash) score of predicted junctions must be≥ 3
Skew score of predicted junction (−log10 probability of unusual coverage evenness) must be≤ 3
Number of bases that at least one read must overlap each uniquely aligned side of a predicted junction≥ 1

Read Alignment Evidence

optionvalue
ModeConsensus/Mixed Base
Ploidy1 (haploid)
Consensus mutation E-value cutoff10
Consensus frequency cutoff0.75
Consensus minimum variant coverage each strandOFF
Consensus minimum total coverage each strandOFF
Consensus minimum variant coverageOFF
Consensus minimum total coverageOFF
Polymorphism E-value cutoff10
Polymorphism frequency cutoff0.2
Polymorphism minimum variant coverage each strandOFF
Polymorphism minimum total coverage each strandOFF
Polymorphism minimum variant coverageOFF
Polymorphism minimum total coverageOFF
Polymorphism bias cutoffOFF
Predict indel polymorphismsYES
Skip indel polymorphisms in homopolymers runs ofOFF
Skip base substitutions when they create a homopolymer flanked on each side byOFF

Software Versions

programversion
bowtie22.3.4.1
R3.4.4

Execution Times

stepstartendelapsed
Read and reference sequence file input01:46:28 02 Apr 201901:47:40 02 Apr 20191 minute 12 seconds
Read alignment to reference genome01:47:41 02 Apr 201902:26:17 02 Apr 201938 minutes 36 seconds
Preprocessing alignments for candidate junction identification02:26:17 02 Apr 201902:27:29 02 Apr 20191 minute 12 seconds
Preliminary analysis of coverage distribution02:27:29 02 Apr 201902:29:40 02 Apr 20192 minutes 11 seconds
Identifying junction candidates02:29:40 02 Apr 201902:29:42 02 Apr 20192 seconds
Re-alignment to junction candidates02:29:42 02 Apr 201902:31:49 02 Apr 20192 minutes 7 seconds
Resolving best read alignments02:31:49 02 Apr 201902:33:43 02 Apr 20191 minute 54 seconds
Creating BAM files02:33:43 02 Apr 201902:35:45 02 Apr 20192 minutes 2 seconds
Tabulating error counts02:35:45 02 Apr 201902:36:19 02 Apr 201934 seconds
Re-calibrating base error rates02:36:19 02 Apr 201902:36:19 02 Apr 20190 seconds
Examining read alignment evidence02:36:19 02 Apr 201902:41:46 02 Apr 20195 minutes 27 seconds
Polymorphism statistics02:41:46 02 Apr 201902:41:46 02 Apr 20190 seconds
Output02:41:46 02 Apr 201902:42:25 02 Apr 201939 seconds
Total 55 minutes 56 seconds