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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsPutida-Van-ACB122-A12-F47-I1-R1_S31_L001_R1_001.good.fq354,44846,040,347100.0%129.9 bases137 bases95.2%
errorsPutida-Van-ACB122-A12-F47-I1-R1_S31_L001_R2_001.good.fq354,44846,040,347100.0%129.9 bases137 bases94.1%
errorsPutida-Van-ACB122-A12-F47-I1-R1_S31_L002_R1_001.good.fq345,77545,013,886100.0%130.2 bases137 bases95.6%
errorsPutida-Van-ACB122-A12-F47-I1-R1_S31_L002_R2_001.good.fq345,77545,013,886100.0%130.2 bases137 bases94.4%
errorsPutida-Van-ACB122-A12-F47-I1-R1_S31_L003_R1_001.good.fq367,53547,924,584100.0%130.4 bases137 bases95.7%
errorsPutida-Van-ACB122-A12-F47-I1-R1_S31_L003_R2_001.good.fq367,53547,924,584100.0%130.4 bases137 bases94.5%
errorsPutida-Van-ACB122-A12-F47-I1-R1_S31_L004_R1_001.good.fq359,34146,793,374100.0%130.2 bases137 bases95.7%
errorsPutida-Van-ACB122-A12-F47-I1-R1_S31_L004_R2_001.good.fq359,34146,793,374100.0%130.2 bases137 bases94.4%
total2,854,198371,544,382100.0%130.2 bases137 bases94.9%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionACB1226,184,09758.02.5100.0%tig00000001|arrow.
total6,184,097100.0%

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≤ 1000001545
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 ≤ 500086
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.004

Junction Skew Score Calculation

reference sequencepr(no read start)
ACB1220.86041

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 input11:13:43 28 Apr 202311:14:31 28 Apr 202348 seconds
Read alignment to reference genome11:14:32 28 Apr 202311:20:39 28 Apr 20236 minutes 7 seconds
Preprocessing alignments for candidate junction identification11:20:39 28 Apr 202311:21:14 28 Apr 202335 seconds
Preliminary analysis of coverage distribution11:21:14 28 Apr 202311:22:52 28 Apr 20231 minute 38 seconds
Identifying junction candidates11:22:52 28 Apr 202311:22:53 28 Apr 20231 second
Re-alignment to junction candidates11:22:53 28 Apr 202311:24:19 28 Apr 20231 minute 26 seconds
Resolving best read alignments11:24:19 28 Apr 202311:25:08 28 Apr 202349 seconds
Creating BAM files11:25:08 28 Apr 202311:26:37 28 Apr 20231 minute 29 seconds
Tabulating error counts11:26:37 28 Apr 202311:27:08 28 Apr 202331 seconds
Re-calibrating base error rates11:27:08 28 Apr 202311:27:11 28 Apr 20233 seconds
Examining read alignment evidence11:27:11 28 Apr 202311:33:54 28 Apr 20236 minutes 43 seconds
Polymorphism statistics11:33:54 28 Apr 202311:33:55 28 Apr 20231 second
Output11:33:55 28 Apr 202311:34:10 28 Apr 202315 seconds
Total 20 minutes 26 seconds