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-Population-4-24_S13_L001_R1_001.good.fq1,240,795309,452,774100.0%249.4 bases281 bases98.1%
errorsC13-Redo-Population-4-24_S13_L001_R2_001.good.fq1,240,795313,355,763100.0%252.5 bases281 bases82.0%
total2,481,590622,808,537100.0%251.0 bases281 bases90.1%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0009134,641,652117.97.2100.0%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≤ 1000002830
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 ≤ 5000389
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.048

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0009130.84911

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≤ 0
Number of bases that at least one read must overlap each uniquely aligned side of a predicted junction≥ 6

Read Alignment Evidence

optionvalue
ModeFull Polymorphism
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 cutoff2
Polymorphism frequency cutoff0.05
Polymorphism minimum variant coverage each strand2
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 of ≥3 bases
Skip base substitutions when they create a homopolymer flanked on each side by ≥5 bases

Software Versions

programversion
bowtie22.3.4.1
R3.4.4

Execution Times

stepstartendelapsed
Read and reference sequence file input16:06:27 16 May 201916:07:06 16 May 201939 seconds
Read alignment to reference genome16:07:06 16 May 201916:21:11 16 May 201914 minutes 5 seconds
Preprocessing alignments for candidate junction identification16:21:11 16 May 201916:21:49 16 May 201938 seconds
Preliminary analysis of coverage distribution16:21:49 16 May 201916:24:08 16 May 20192 minutes 19 seconds
Identifying junction candidates16:24:08 16 May 201916:24:11 16 May 20193 seconds
Re-alignment to junction candidates16:24:11 16 May 201916:27:26 16 May 20193 minutes 15 seconds
Resolving best read alignments16:27:26 16 May 201916:28:35 16 May 20191 minute 9 seconds
Creating BAM files16:28:35 16 May 201916:30:33 16 May 20191 minute 58 seconds
Tabulating error counts16:30:33 16 May 201916:31:25 16 May 201952 seconds
Re-calibrating base error rates16:31:25 16 May 201916:31:26 16 May 20191 second
Examining read alignment evidence16:31:26 16 May 201917:39:56 16 May 20191 hour 8 minutes 30 seconds
Polymorphism statistics17:39:56 16 May 201917:39:56 16 May 20190 seconds
Output17:39:56 16 May 201917:40:10 16 May 201914 seconds
Total 1 hour 33 minutes 43 seconds