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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsPputida_TALE__HGL_Pputida_117_S105_L001_R1_001.good.fq6,038,176898,873,488100.0%148.9 bases150 bases96.4%
errorsPputida_TALE__HGL_Pputida_117_S105_L001_R2_001.good.fq6,038,176898,873,488100.0%148.9 bases150 bases95.8%
total12,076,3521,797,746,976100.0%148.9 bases150 bases96.1%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0029476,181,929278.94.5100.0%Pseudomonas putida KT2440 chromosome, complete genome.
total6,181,929100.0%

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 ≤ 50001461
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.073

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0029470.54691

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 input13:44:45 26 Mar 202013:47:53 26 Mar 20203 minutes 8 seconds
Read alignment to reference genome13:47:53 26 Mar 202014:13:58 26 Mar 202026 minutes 5 seconds
Preprocessing alignments for candidate junction identification14:13:58 26 Mar 202014:16:52 26 Mar 20202 minutes 54 seconds
Preliminary analysis of coverage distribution14:16:52 26 Mar 202014:22:18 26 Mar 20205 minutes 26 seconds
Identifying junction candidates14:22:18 26 Mar 202014:36:05 26 Mar 202013 minutes 47 seconds
Re-alignment to junction candidates14:36:05 26 Mar 202014:43:46 26 Mar 20207 minutes 41 seconds
Resolving best read alignments14:43:46 26 Mar 202014:49:24 26 Mar 20205 minutes 38 seconds
Creating BAM files14:49:24 26 Mar 202014:54:10 26 Mar 20204 minutes 46 seconds
Tabulating error counts14:54:10 26 Mar 202014:56:48 26 Mar 20202 minutes 38 seconds
Re-calibrating base error rates14:56:48 26 Mar 202014:56:49 26 Mar 20201 second
Examining read alignment evidence14:56:49 26 Mar 202015:22:49 26 Mar 202026 minutes 0 seconds
Polymorphism statistics15:22:49 26 Mar 202015:22:59 26 Mar 202010 seconds
Output15:22:59 26 Mar 202015:24:14 26 Mar 20201 minute 15 seconds
Total 1 hour 39 minutes 29 seconds