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-9-3_S17_L001_R2_001.good.fq1,218,830324,577,308100.0%266.3 bases289 bases97.5%
errorspgi-9-3_S17_L001_R1_001.good.fq1,218,830324,353,953100.0%266.1 bases289 bases99.7%
total2,437,660648,931,261100.0%266.2 bases289 bases98.6%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0009134,641,653140.83.9100.0%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≤ 1000005033
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 ≤ 5000399
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.050

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0009130.83576

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 input12:32:22 18 Mar 201812:33:18 18 Mar 201856 seconds
Read alignment to reference genome12:33:18 18 Mar 201812:52:53 18 Mar 201819 minutes 35 seconds
Preprocessing alignments for candidate junction identification12:52:53 18 Mar 201812:54:14 18 Mar 20181 minute 21 seconds
Preliminary analysis of coverage distribution12:54:14 18 Mar 201812:57:05 18 Mar 20182 minutes 51 seconds
Identifying junction candidates12:57:05 18 Mar 201812:57:13 18 Mar 20188 seconds
Re-alignment to junction candidates12:57:13 18 Mar 201812:59:37 18 Mar 20182 minutes 24 seconds
Resolving best read alignments12:59:37 18 Mar 201813:01:32 18 Mar 20181 minute 55 seconds
Creating BAM files13:01:32 18 Mar 201813:03:24 18 Mar 20181 minute 52 seconds
Tabulating error counts13:03:24 18 Mar 201813:04:41 18 Mar 20181 minute 17 seconds
Re-calibrating base error rates13:04:41 18 Mar 201813:04:42 18 Mar 20181 second
Examining read alignment evidence13:04:42 18 Mar 201814:28:40 18 Mar 20181 hour 23 minutes 58 seconds
Polymorphism statistics14:28:40 18 Mar 201814:28:41 18 Mar 20181 second
Output14:28:41 18 Mar 201814:29:09 18 Mar 201828 seconds
Total 1 hour 56 minutes 47 seconds