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-2-23_S8_L001_R1_001.good.fq1,196,780294,867,437100.0%246.4 bases275 bases98.1%
errorsc13-Redo-2-23_S8_L001_R2_001.good.fq1,196,780296,032,329100.0%247.4 bases275 bases88.8%
total2,393,560590,899,766100.0%246.9 bases275 bases93.5%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0009134,641,652119.84.6100.0%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≤ 1000003582
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 ≤ 5000411
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.049

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0009130.84978

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 input15:06:20 16 May 201915:06:57 16 May 201937 seconds
Read alignment to reference genome15:06:57 16 May 201915:20:13 16 May 201913 minutes 16 seconds
Preprocessing alignments for candidate junction identification15:20:13 16 May 201915:20:52 16 May 201939 seconds
Preliminary analysis of coverage distribution15:20:52 16 May 201915:23:10 16 May 20192 minutes 18 seconds
Identifying junction candidates15:23:10 16 May 201915:23:16 16 May 20196 seconds
Re-alignment to junction candidates15:23:16 16 May 201915:26:15 16 May 20192 minutes 59 seconds
Resolving best read alignments15:26:15 16 May 201915:27:22 16 May 20191 minute 7 seconds
Creating BAM files15:27:22 16 May 201915:29:22 16 May 20192 minutes 0 seconds
Tabulating error counts15:29:22 16 May 201915:30:14 16 May 201952 seconds
Re-calibrating base error rates15:30:14 16 May 201915:30:15 16 May 20191 second
Examining read alignment evidence15:30:15 16 May 201915:39:28 16 May 20199 minutes 13 seconds
Polymorphism statistics15:39:28 16 May 201915:39:28 16 May 20190 seconds
Output15:39:28 16 May 201915:39:40 16 May 201912 seconds
Total 33 minutes 20 seconds