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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsJBEI_Galactose_A30_F2_I4_S5_R1_001.good.fq289,27738,522,201100.0%133.2 bases136 bases95.6%
errorsJBEI_Galactose_A30_F2_I4_S5_R2_001.good.fq289,27738,522,201100.0%133.2 bases136 bases82.1%
total578,55477,044,402100.0%133.2 bases136 bases88.8%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0029476,186,8788.92.8100.0%Pseudomonas putida KT2440 chromosome, complete genome.
total6,186,878100.0%

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≤ 1000003167
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 ≤ 5000141
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.006

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0029470.96714

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 input05:03:35 19 Jul 202005:03:52 19 Jul 202017 seconds
Read alignment to reference genome05:03:53 19 Jul 202005:05:16 19 Jul 20201 minute 23 seconds
Preprocessing alignments for candidate junction identification05:05:16 19 Jul 202005:05:30 19 Jul 202014 seconds
Preliminary analysis of coverage distribution05:05:30 19 Jul 202005:05:49 19 Jul 202019 seconds
Identifying junction candidates05:05:49 19 Jul 202005:05:50 19 Jul 20201 second
Re-alignment to junction candidates05:05:50 19 Jul 202005:06:08 19 Jul 202018 seconds
Resolving best read alignments05:06:08 19 Jul 202005:06:29 19 Jul 202021 seconds
Creating BAM files05:06:29 19 Jul 202005:06:45 19 Jul 202016 seconds
Tabulating error counts05:06:45 19 Jul 202005:06:55 19 Jul 202010 seconds
Re-calibrating base error rates05:06:55 19 Jul 202005:06:56 19 Jul 20201 second
Examining read alignment evidence05:06:56 19 Jul 202005:09:43 19 Jul 20202 minutes 47 seconds
Polymorphism statistics05:09:43 19 Jul 202005:09:48 19 Jul 20205 seconds
Output05:09:48 19 Jul 202005:21:51 19 Jul 202012 minutes 3 seconds
Total 18 minutes 15 seconds