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

Read File Information

read filereadsbasespassed filtersaveragelongestmapped
errorsPputida_PALE__HGL_Pputida_166_S154_L001_R1_001.good.fq4,523,043674,031,530100.0%149.0 bases150 bases97.8%
errorsPputida_PALE__HGL_Pputida_166_S154_L001_R2_001.good.fq4,523,043674,031,530100.0%149.0 bases150 bases97.3%
total9,046,0861,348,063,060100.0%149.0 bases150 bases97.5%

Reference Sequence Information

seq idlengthfit meanfit dispersion% mapped readsdescription
coveragedistributionNC_0029476,183,858212.74.3100.0%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≤ 10000081858
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 ≤ 50001117
Total length of all junction candidates (factor times the reference genome length)≤ 0.10.056

Junction Skew Score Calculation

reference sequencepr(no read start)
NC_0029470.60478

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 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 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
bowtie22.3.4.1
R3.4.4

Execution Times

stepstartendelapsed
Read and reference sequence file input05:55:44 07 Apr 202005:59:25 07 Apr 20203 minutes 41 seconds
Read alignment to reference genome05:59:26 07 Apr 202006:18:51 07 Apr 202019 minutes 25 seconds
Preprocessing alignments for candidate junction identification06:18:51 07 Apr 202006:22:45 07 Apr 20203 minutes 54 seconds
Preliminary analysis of coverage distribution06:22:45 07 Apr 202006:27:04 07 Apr 20204 minutes 19 seconds
Identifying junction candidates06:27:04 07 Apr 202006:41:34 07 Apr 202014 minutes 30 seconds
Re-alignment to junction candidates06:41:34 07 Apr 202006:47:24 07 Apr 20205 minutes 50 seconds
Resolving best read alignments06:47:24 07 Apr 202006:54:36 07 Apr 20207 minutes 12 seconds
Creating BAM files06:54:36 07 Apr 202006:58:05 07 Apr 20203 minutes 29 seconds
Tabulating error counts06:58:05 07 Apr 202007:01:33 07 Apr 20203 minutes 28 seconds
Re-calibrating base error rates07:01:33 07 Apr 202007:01:35 07 Apr 20202 seconds
Examining read alignment evidence07:01:35 07 Apr 202008:28:14 07 Apr 20201 hour 26 minutes 39 seconds
Polymorphism statistics08:28:14 07 Apr 202008:28:29 07 Apr 202015 seconds
Output08:28:29 07 Apr 202008:36:44 07 Apr 20208 minutes 15 seconds
Total 2 hours 40 minutes 59 seconds