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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsEEP_appC-cydB-ndh_A12F22I0R1_S40_L003_R1_001.good.fq2,754,323412,694,483100.0%149.8 bases150 bases99.4%
errorsEEP_appC-cydB-ndh_A12F22I0R1_S40_L003_R2_001.good.fq2,754,323412,694,483100.0%149.8 bases150 bases98.8%
total5,508,646825,388,966100.0%149.8 bases150 bases99.1%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0009134,641,652171.46.6100.0%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≤ 10000016073
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 ≤ 5000240
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_0009130.77334

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≤ 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
bowtie22.2.6
R3.4.4

Execution Times

stepstartendelapsed
Read and reference sequence file input20:40:00 15 Apr 202120:41:35 15 Apr 20211 minute 35 seconds
Read alignment to reference genome20:41:36 15 Apr 202120:54:44 15 Apr 202113 minutes 8 seconds
Preprocessing alignments for candidate junction identification20:54:44 15 Apr 202120:55:53 15 Apr 20211 minute 9 seconds
Preliminary analysis of coverage distribution20:55:53 15 Apr 202120:58:42 15 Apr 20212 minutes 49 seconds
Identifying junction candidates20:58:42 15 Apr 202120:58:44 15 Apr 20212 seconds
Re-alignment to junction candidates20:58:44 15 Apr 202121:01:57 15 Apr 20213 minutes 13 seconds
Resolving best read alignments21:01:57 15 Apr 202121:03:35 15 Apr 20211 minute 38 seconds
Creating BAM files21:03:35 15 Apr 202121:06:04 15 Apr 20212 minutes 29 seconds
Tabulating error counts21:06:04 15 Apr 202121:07:15 15 Apr 20211 minute 11 seconds
Re-calibrating base error rates21:07:15 15 Apr 202121:07:16 15 Apr 20211 second
Examining read alignment evidence21:07:16 15 Apr 202122:00:14 15 Apr 202152 minutes 58 seconds
Polymorphism statistics22:00:14 15 Apr 202122:00:17 15 Apr 20213 seconds
Output22:00:17 15 Apr 202122:00:43 15 Apr 202126 seconds
Total 1 hour 20 minutes 42 seconds