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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsCCK_gndEvo02EP_Isolate_1_S1627_L005_R1_001.good.fq1,296,014184,681,379100.0%142.5 bases143 bases94.6%
errorsCCK_gndEvo02EP_Isolate_1_S1627_L005_R2_001.good.fq1,296,014184,681,379100.0%142.5 bases143 bases86.4%
total2,592,028369,362,758100.0%142.5 bases143 bases90.5%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0009134,641,65271.41.9100.0%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≤ 10000015220
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 ≤ 5000247
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.016

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0009130.81440

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 input20:09:49 26 Feb 202020:10:28 26 Feb 202039 seconds
Read alignment to reference genome20:10:28 26 Feb 202020:18:48 26 Feb 20208 minutes 20 seconds
Preprocessing alignments for candidate junction identification20:18:48 26 Feb 202020:19:25 26 Feb 202037 seconds
Preliminary analysis of coverage distribution20:19:25 26 Feb 202020:20:57 26 Feb 20201 minute 32 seconds
Identifying junction candidates20:20:57 26 Feb 202020:21:00 26 Feb 20203 seconds
Re-alignment to junction candidates20:21:00 26 Feb 202020:23:02 26 Feb 20202 minutes 2 seconds
Resolving best read alignments20:23:02 26 Feb 202020:23:56 26 Feb 202054 seconds
Creating BAM files20:23:56 26 Feb 202020:25:21 26 Feb 20201 minute 25 seconds
Tabulating error counts20:25:21 26 Feb 202020:25:47 26 Feb 202026 seconds
Re-calibrating base error rates20:25:47 26 Feb 202020:25:48 26 Feb 20201 second
Examining read alignment evidence20:25:48 26 Feb 202020:31:20 26 Feb 20205 minutes 32 seconds
Polymorphism statistics20:31:20 26 Feb 202020:31:20 26 Feb 20200 seconds
Output20:31:20 26 Feb 202020:31:35 26 Feb 202015 seconds
Total 21 minutes 46 seconds