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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsC13-Redo-5-135_S5_L001_R1_001.good.fq2,357,205594,481,637100.0%252.2 bases289 bases99.1%
errorsC13-Redo-5-135_S5_L001_R2_001.good.fq2,357,205597,901,424100.0%253.6 bases289 bases91.2%
total4,714,4101,192,383,061100.0%252.9 bases289 bases95.1%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0009134,641,652249.36.0100.0%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≤ 1000008021
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 ≤ 5000757
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.095

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0009130.75224

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 input06:06:45 16 May 201906:08:10 16 May 20191 minute 25 seconds
Read alignment to reference genome06:08:10 16 May 201906:32:34 16 May 201924 minutes 24 seconds
Preprocessing alignments for candidate junction identification06:32:34 16 May 201906:33:49 16 May 20191 minute 15 seconds
Preliminary analysis of coverage distribution06:33:49 16 May 201906:38:17 16 May 20194 minutes 28 seconds
Identifying junction candidates06:38:17 16 May 201906:38:30 16 May 201913 seconds
Re-alignment to junction candidates06:38:30 16 May 201906:46:01 16 May 20197 minutes 31 seconds
Resolving best read alignments06:46:01 16 May 201906:48:17 16 May 20192 minutes 16 seconds
Creating BAM files06:48:17 16 May 201906:52:06 16 May 20193 minutes 49 seconds
Tabulating error counts06:52:06 16 May 201906:53:51 16 May 20191 minute 45 seconds
Re-calibrating base error rates06:53:51 16 May 201906:53:52 16 May 20191 second
Examining read alignment evidence06:53:52 16 May 201907:12:09 16 May 201918 minutes 17 seconds
Polymorphism statistics07:12:09 16 May 201907:12:09 16 May 20190 seconds
Output07:12:09 16 May 201907:12:37 16 May 201928 seconds
Total 1 hour 5 minutes 52 seconds