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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsPputida_sub_A2_F72_I1_R1_001.good.fq5,448,446808,129,857100.0%148.3 bases150 bases96.8%
errorsPputida_sub_A2_F72_I1_R2_001.good.fq5,448,446808,129,857100.0%148.3 bases150 bases96.2%
total10,896,8921,616,259,714100.0%148.3 bases150 bases96.5%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0029476,183,858251.24.2100.0%na
total6,183,858100.0%

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≤ 100000100003
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 ≤ 5000917
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_0029470.56296

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 input05:21:28 03 Feb 202105:31:38 03 Feb 202110 minutes 10 seconds
Read alignment to reference genome05:31:39 03 Feb 202106:54:39 03 Feb 20211 hour 23 minutes 0 seconds
Preprocessing alignments for candidate junction identification06:54:39 03 Feb 202107:04:28 03 Feb 20219 minutes 49 seconds
Preliminary analysis of coverage distribution07:04:28 03 Feb 202107:22:19 03 Feb 202117 minutes 51 seconds
Identifying junction candidates07:22:19 03 Feb 202107:41:10 03 Feb 202118 minutes 51 seconds
Re-alignment to junction candidates07:41:10 03 Feb 202108:04:33 03 Feb 202123 minutes 23 seconds
Resolving best read alignments08:04:33 03 Feb 202108:17:32 03 Feb 202112 minutes 59 seconds
Creating BAM files08:17:32 03 Feb 202108:33:32 03 Feb 202116 minutes 0 seconds
Tabulating error counts08:33:32 03 Feb 202108:41:03 03 Feb 20217 minutes 31 seconds
Re-calibrating base error rates08:41:03 03 Feb 202108:41:06 03 Feb 20213 seconds
Examining read alignment evidence08:41:06 03 Feb 202110:10:11 03 Feb 20211 hour 29 minutes 5 seconds
Polymorphism statistics10:10:11 03 Feb 202110:10:25 03 Feb 202114 seconds
Output10:10:25 03 Feb 202110:12:22 03 Feb 20211 minute 57 seconds
Total 4 hours 50 minutes 53 seconds