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_15_40_1_S213_S1991_L006_R1_001.good.fq1,387,416187,138,928100.0%134.9 bases141 bases85.4%
errorsSNFM_15_40_1_S213_S1991_L006_R2_001.good.fq1,387,416187,138,928100.0%134.9 bases141 bases84.7%
total2,774,832374,277,856100.0%134.9 bases141 bases85.1%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionCP0007302,872,915109.62.3100.0%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≤ 100000100000
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 ≤ 5000263
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.027

Junction Skew Score Calculation

reference sequencepr(no read start)
CP0007300.70399

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≤ 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 cutoff0.8
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
bowtie22.3.4.3
R3.5.1

Execution Times

stepstartendelapsed
Read and reference sequence file input11:24:29 26 Oct 201811:25:21 26 Oct 201852 seconds
Read alignment to reference genome11:25:21 26 Oct 201811:31:29 26 Oct 20186 minutes 8 seconds
Preprocessing alignments for candidate junction identification11:31:29 26 Oct 201811:32:13 26 Oct 201844 seconds
Preliminary analysis of coverage distribution11:32:13 26 Oct 201811:33:19 26 Oct 20181 minute 6 seconds
Identifying junction candidates11:33:19 26 Oct 201811:34:19 26 Oct 20181 minute 0 seconds
Re-alignment to junction candidates11:34:19 26 Oct 201811:35:59 26 Oct 20181 minute 40 seconds
Resolving best read alignments11:35:59 26 Oct 201811:37:16 26 Oct 20181 minute 17 seconds
Creating BAM files11:37:16 26 Oct 201811:38:14 26 Oct 201858 seconds
Tabulating error counts11:38:14 26 Oct 201811:38:38 26 Oct 201824 seconds
Re-calibrating base error rates11:38:38 26 Oct 201811:38:39 26 Oct 20181 second
Examining read alignment evidence11:38:39 26 Oct 201811:41:50 26 Oct 20183 minutes 11 seconds
Polymorphism statistics11:41:50 26 Oct 201811:41:51 26 Oct 20181 second
Output11:41:51 26 Oct 201811:42:00 26 Oct 20189 seconds
Total 17 minutes 31 seconds