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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsSRR14920161_R1.good.fq11,644,7461,609,245,163100.0%138.2 bases140 bases99.5%
errorsSRR14920161_R2.good.fq11,644,7461,609,245,163100.0%138.2 bases140 bases97.6%
total23,289,4923,218,490,326100.0%138.2 bases140 bases98.5%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNZ_CP0252684,643,559700.426.4100.0%Escherichia coli str. K-12 substr. MG1655 strain K-12 chromosome,
total4,643,559100.0%

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≤ 10000037356
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 ≤ 5000620
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.039

Junction Skew Score Calculation

reference sequencepr(no read start)
NZ_CP0252680.48212

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 input23:29:22 05 Mar 202323:35:06 05 Mar 20235 minutes 44 seconds
Read alignment to reference genome23:35:06 05 Mar 202300:24:59 06 Mar 202349 minutes 53 seconds
Preprocessing alignments for candidate junction identification00:24:59 06 Mar 202300:31:26 06 Mar 20236 minutes 27 seconds
Preliminary analysis of coverage distribution00:31:26 06 Mar 202300:42:31 06 Mar 202311 minutes 5 seconds
Identifying junction candidates00:42:31 06 Mar 202300:45:55 06 Mar 20233 minutes 24 seconds
Re-alignment to junction candidates00:45:55 06 Mar 202301:00:30 06 Mar 202314 minutes 35 seconds
Resolving best read alignments01:00:30 06 Mar 202301:08:35 06 Mar 20238 minutes 5 seconds
Creating BAM files01:08:35 06 Mar 202301:18:18 06 Mar 20239 minutes 43 seconds
Tabulating error counts01:18:18 06 Mar 202301:22:55 06 Mar 20234 minutes 37 seconds
Re-calibrating base error rates01:22:55 06 Mar 202301:22:57 06 Mar 20232 seconds
Examining read alignment evidence01:22:57 06 Mar 202302:22:11 06 Mar 202359 minutes 14 seconds
Polymorphism statistics02:22:11 06 Mar 202302:22:12 06 Mar 20231 second
Output02:22:12 06 Mar 202302:24:37 06 Mar 20232 minutes 25 seconds
Total 2 hours 55 minutes 15 seconds