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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsPputida_sub_A6_F90_I1_R1_001.good.fq8,197,7001,177,145,147100.0%143.6 bases150 bases95.0%
errorsPputida_sub_A6_F90_I1_R2_001.good.fq8,197,7001,177,145,147100.0%143.6 bases150 bases94.4%
total16,395,4002,354,290,294100.0%143.6 bases150 bases94.7%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0029476,186,878359.57.5100.0%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≤ 100000100000
Coverage evenness (position-hash) score of junction candidates≥ 2≥ 3
Test this many junction candidates (n). May be smaller if not enough passed the coverage evenness threshold100 ≤ n ≤ 5000602
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.030

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0029470.44363

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≤ 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
bowtie22.2.6
R3.4.4

Execution Times

stepstartendelapsed
Read and reference sequence file input08:28:38 05 Mar 202108:33:14 05 Mar 20214 minutes 36 seconds
Read alignment to reference genome08:33:15 05 Mar 202109:13:40 05 Mar 202140 minutes 25 seconds
Preprocessing alignments for candidate junction identification09:13:40 05 Mar 202109:17:30 05 Mar 20213 minutes 50 seconds
Preliminary analysis of coverage distribution09:17:30 05 Mar 202109:25:15 05 Mar 20217 minutes 45 seconds
Identifying junction candidates09:25:15 05 Mar 202109:27:46 05 Mar 20212 minutes 31 seconds
Re-alignment to junction candidates09:27:46 05 Mar 202109:38:21 05 Mar 202110 minutes 35 seconds
Resolving best read alignments09:38:21 05 Mar 202109:43:55 05 Mar 20215 minutes 34 seconds
Creating BAM files09:43:55 05 Mar 202109:50:50 05 Mar 20216 minutes 55 seconds
Tabulating error counts09:50:50 05 Mar 202109:54:14 05 Mar 20213 minutes 24 seconds
Re-calibrating base error rates09:54:14 05 Mar 202109:54:16 05 Mar 20212 seconds
Examining read alignment evidence09:54:16 05 Mar 202110:33:23 05 Mar 202139 minutes 7 seconds
Polymorphism statistics10:33:23 05 Mar 202110:33:41 05 Mar 202118 seconds
Output10:33:41 05 Mar 202110:34:27 05 Mar 202146 seconds
Total 2 hours 5 minutes 48 seconds