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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsSRR14920167_R1.good.fq5,604,728778,452,297100.0%138.9 bases140 bases99.2%
errorsSRR14920167_R2.good.fq5,604,728778,452,297100.0%138.9 bases140 bases95.3%
total11,209,4561,556,904,594100.0%138.9 bases140 bases97.2%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNZ_CP0252684,643,559341.914.1100.0%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≤ 10000016736
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 ≤ 5000782
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.049

Junction Skew Score Calculation

reference sequencepr(no read start)
NZ_CP0252680.64974

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 input22:58:15 03 Mar 202323:01:02 03 Mar 20232 minutes 47 seconds
Read alignment to reference genome23:01:02 03 Mar 202323:25:48 03 Mar 202324 minutes 46 seconds
Preprocessing alignments for candidate junction identification23:25:48 03 Mar 202323:28:21 03 Mar 20232 minutes 33 seconds
Preliminary analysis of coverage distribution23:28:21 03 Mar 202323:34:30 03 Mar 20236 minutes 9 seconds
Identifying junction candidates23:34:30 03 Mar 202323:34:59 03 Mar 202329 seconds
Re-alignment to junction candidates23:34:59 03 Mar 202323:42:34 03 Mar 20237 minutes 35 seconds
Resolving best read alignments23:42:34 03 Mar 202323:46:27 03 Mar 20233 minutes 53 seconds
Creating BAM files23:46:27 03 Mar 202323:51:56 03 Mar 20235 minutes 29 seconds
Tabulating error counts23:51:56 03 Mar 202323:54:20 03 Mar 20232 minutes 24 seconds
Re-calibrating base error rates23:54:20 03 Mar 202323:54:21 03 Mar 20231 second
Examining read alignment evidence23:54:21 03 Mar 202300:23:00 04 Mar 202328 minutes 39 seconds
Polymorphism statistics00:23:00 04 Mar 202300:23:01 04 Mar 20231 second
Output00:23:01 04 Mar 202300:24:43 04 Mar 20231 minute 42 seconds
Total 1 hour 26 minutes 28 seconds