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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsJADR46_end_pooled_R1.good.fq5,850,485877,508,415100.0%150.0 bases150 bases99.6%
errorsJADR46_end_pooled_R2.good.fq5,850,485877,508,415100.0%150.0 bases150 bases99.6%
total11,700,9701,755,016,830100.0%150.0 bases150 bases99.6%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionCP0068814,033,459414.67.593.9%Bacillus subtilis PY79, complete genome.
coveragedistributionExported6,53817063.9142.06.1%natural circular DNA
total4,039,997100.0%

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≤ 10000035757
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 ≤ 5000149
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.011

Junction Skew Score Calculation

reference sequencepr(no read start)
CP0068810.30354
Exported0.02875

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 input11:50:34 20 Jan 202111:54:04 20 Jan 20213 minutes 30 seconds
Read alignment to reference genome11:54:04 20 Jan 202112:20:17 20 Jan 202126 minutes 13 seconds
Preprocessing alignments for candidate junction identification12:20:18 20 Jan 202112:23:02 20 Jan 20212 minutes 44 seconds
Preliminary analysis of coverage distribution12:23:02 20 Jan 202112:32:35 20 Jan 20219 minutes 33 seconds
Identifying junction candidates12:32:35 20 Jan 202112:32:37 20 Jan 20212 seconds
Re-alignment to junction candidates12:32:37 20 Jan 202112:40:28 20 Jan 20217 minutes 51 seconds
Resolving best read alignments12:40:28 20 Jan 202112:44:34 20 Jan 20214 minutes 6 seconds
Creating BAM files12:44:34 20 Jan 202112:53:30 20 Jan 20218 minutes 56 seconds
Tabulating error counts12:53:30 20 Jan 202112:56:18 20 Jan 20212 minutes 48 seconds
Re-calibrating base error rates12:56:18 20 Jan 202112:56:20 20 Jan 20212 seconds
Examining read alignment evidence12:56:20 20 Jan 202116:32:54 20 Jan 20213 hours 36 minutes 34 seconds
Polymorphism statistics16:32:54 20 Jan 202116:32:56 20 Jan 20212 seconds
Output16:32:56 20 Jan 202116:34:29 20 Jan 20211 minute 33 seconds
Total 4 hours 43 minutes 54 seconds