breseq  version 0.32.0  revision 6ff6de7d1b87
mutation predictions | marginal predictions | summary statistics | genome diff | command line log

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorspgi-10-1_S18_L001_R2_001.good.fq904,252240,656,608100.0%266.1 bases289 bases94.0%
errorspgi-10-1_S18_L001_R1_001.good.fq904,252239,970,901100.0%265.4 bases289 bases99.6%
total1,808,504480,627,509100.0%265.8 bases289 bases96.8%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0009134,641,65399.73.7100.0%Escherichia coli str. K-12 sbstr. MG1655, complete genome. Live strain from Systems Biology Research Group
total4,641,653100.0%

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≤ 1000004972
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 ≤ 5000363
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.046

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0009130.87177

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≤ 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 cutoffOFF
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 cutoff0.025
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
bowtie22.2.8
R3.3.1

Execution Times

stepstartendelapsed
Read and reference sequence file input17:44:13 19 Mar 201817:44:40 19 Mar 201827 seconds
Read alignment to reference genome17:44:40 19 Mar 201817:47:19 19 Mar 20182 minutes 39 seconds
Preprocessing alignments for candidate junction identification17:47:19 19 Mar 201817:47:51 19 Mar 201832 seconds
Preliminary analysis of coverage distribution17:47:51 19 Mar 201817:49:06 19 Mar 20181 minute 15 seconds
Identifying junction candidates17:49:06 19 Mar 201817:49:12 19 Mar 20186 seconds
Re-alignment to junction candidates17:49:12 19 Mar 201817:49:40 19 Mar 201828 seconds
Resolving best read alignments17:49:40 19 Mar 201817:50:37 19 Mar 201857 seconds
Creating BAM files17:50:37 19 Mar 201817:51:37 19 Mar 20181 minute 0 seconds
Tabulating error counts17:51:37 19 Mar 201817:52:18 19 Mar 201841 seconds
Re-calibrating base error rates17:52:18 19 Mar 201817:52:19 19 Mar 20181 second
Examining read alignment evidence17:52:19 19 Mar 201818:45:27 19 Mar 201853 minutes 8 seconds
Polymorphism statistics18:45:27 19 Mar 201818:45:27 19 Mar 20180 seconds
Output18:45:27 19 Mar 201818:45:44 19 Mar 201817 seconds
Total 1 hour 1 minute 31 seconds