breseq  version 0.35.4  revision f352f80f4bc9
mutation predictions | marginal predictions | summary statistics | genome diff | command line log

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsSRR2191572_R1.good.fq1,268,671238,635,100100.0%188.1 bases457 bases87.9%
total1,268,671238,635,100100.0%188.1 bases457 bases87.9%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0009134,641,65244.11.7100.0%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≤ 10000038795
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 ≤ 5000406
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.080

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0009130.90680

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
Minimum probablilty assigned that no mapped read will start at a given position and strand for junction prediction0.1
Junction allow suboptimal matchesFALSE
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
bowtie22.2.6
R3.4.4

Execution Times

stepstartendelapsed
Read and reference sequence file input16:09:34 17 Nov 202016:10:07 17 Nov 202033 seconds
Read alignment to reference genome16:10:07 17 Nov 202016:15:47 17 Nov 20205 minutes 40 seconds
Preprocessing alignments for candidate junction identification16:15:47 17 Nov 202016:16:13 17 Nov 202026 seconds
Preliminary analysis of coverage distribution16:16:13 17 Nov 202016:17:23 17 Nov 20201 minute 10 seconds
Identifying junction candidates16:17:23 17 Nov 202016:17:37 17 Nov 202014 seconds
Re-alignment to junction candidates16:17:37 17 Nov 202016:19:04 17 Nov 20201 minute 27 seconds
Resolving best read alignments16:19:04 17 Nov 202016:19:38 17 Nov 202034 seconds
Creating BAM files16:19:38 17 Nov 202016:20:43 17 Nov 20201 minute 5 seconds
Tabulating error counts16:20:43 17 Nov 202016:21:08 17 Nov 202025 seconds
Re-calibrating base error rates16:21:08 17 Nov 202016:21:08 17 Nov 20200 seconds
Examining read alignment evidence16:21:08 17 Nov 202016:26:10 17 Nov 20205 minutes 2 seconds
Polymorphism statistics16:26:10 17 Nov 202016:26:18 17 Nov 20208 seconds
Output16:26:18 17 Nov 202016:26:37 17 Nov 202019 seconds
Total 17 minutes 3 seconds