breseq  version 0.33.1  revision 8505477f25b3
mutation predictions | marginal predictions | summary statistics | genome diff | command line log

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsSNFM_19_18_0_S230_S1990_L006_R1_001.good.fq1,087,581152,749,138100.0%140.4 bases141 bases91.4%
errorsSNFM_19_18_0_S230_S1990_L006_R2_001.good.fq1,087,581152,749,138100.0%140.4 bases141 bases90.6%
total2,175,162305,498,276100.0%140.4 bases141 bases91.0%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionCP0007302,872,91596.52.1100.0%Staphylococcus aureus subsp. aureus USA300_TCH1516, complete genome.
total2,872,915100.0%

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≤ 10000024080
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 ≤ 5000656
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.066

Junction Skew Score Calculation

reference sequencepr(no read start)
CP0007300.74275

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 cutoff0.05
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
bowtie22.3.4.3
R3.5.1

Execution Times

stepstartendelapsed
Read and reference sequence file input14:33:49 26 Oct 201814:34:30 26 Oct 201841 seconds
Read alignment to reference genome14:34:30 26 Oct 201814:39:11 26 Oct 20184 minutes 41 seconds
Preprocessing alignments for candidate junction identification14:39:11 26 Oct 201814:39:44 26 Oct 201833 seconds
Preliminary analysis of coverage distribution14:39:44 26 Oct 201814:40:41 26 Oct 201857 seconds
Identifying junction candidates14:40:41 26 Oct 201814:40:46 26 Oct 20185 seconds
Re-alignment to junction candidates14:40:46 26 Oct 201814:42:19 26 Oct 20181 minute 33 seconds
Resolving best read alignments14:42:19 26 Oct 201814:43:19 26 Oct 20181 minute 0 seconds
Creating BAM files14:43:19 26 Oct 201814:44:09 26 Oct 201850 seconds
Tabulating error counts14:44:09 26 Oct 201814:44:29 26 Oct 201820 seconds
Re-calibrating base error rates14:44:29 26 Oct 201814:44:29 26 Oct 20180 seconds
Examining read alignment evidence14:44:29 26 Oct 201814:53:53 26 Oct 20189 minutes 24 seconds
Polymorphism statistics14:53:53 26 Oct 201814:53:54 26 Oct 20181 second
Output14:53:54 26 Oct 201814:54:24 26 Oct 201830 seconds
Total 20 minutes 35 seconds