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_HGL_73_S287_L002_R1_001.good.fq1,482,303198,004,394100.0%133.6 bases150 bases92.6%
errorsPputida_HGL_73_S287_L002_R2_001.good.fq1,482,303198,004,394100.0%133.6 bases150 bases90.4%
total2,964,606396,008,788100.0%133.6 bases150 bases91.5%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0029476,181,92958.22.9100.0%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≤ 100000100003
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 ≤ 50001760
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.088

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0029470.81879

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 input05:20:15 30 Mar 202005:21:00 30 Mar 202045 seconds
Read alignment to reference genome05:21:00 30 Mar 202005:27:45 30 Mar 20206 minutes 45 seconds
Preprocessing alignments for candidate junction identification05:27:45 30 Mar 202005:28:27 30 Mar 202042 seconds
Preliminary analysis of coverage distribution05:28:27 30 Mar 202005:30:00 30 Mar 20201 minute 33 seconds
Identifying junction candidates05:30:00 30 Mar 202005:57:12 30 Mar 202027 minutes 12 seconds
Re-alignment to junction candidates05:57:12 30 Mar 202005:59:15 30 Mar 20202 minutes 3 seconds
Resolving best read alignments05:59:15 30 Mar 202006:00:30 30 Mar 20201 minute 15 seconds
Creating BAM files06:00:30 30 Mar 202006:01:55 30 Mar 20201 minute 25 seconds
Tabulating error counts06:01:55 30 Mar 202006:02:24 30 Mar 202029 seconds
Re-calibrating base error rates06:02:24 30 Mar 202006:02:25 30 Mar 20201 second
Examining read alignment evidence06:02:25 30 Mar 202006:08:12 30 Mar 20205 minutes 47 seconds
Polymorphism statistics06:08:12 30 Mar 202006:08:13 30 Mar 20201 second
Output06:08:13 30 Mar 202006:09:16 30 Mar 20201 minute 3 seconds
Total 49 minutes 1 second