breseq version 0.32.0b
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
read file | reads | bases | passed filters | average | longest | mapped | |
---|---|---|---|---|---|---|---|
errors | A10_F030_R2_F20_I30_S2169_L001_R2_001.good.fq | 2,672,666 | 397,513,894 | 100.0% | 148.7 bases | 149 bases | 93.9% |
errors | A10_F030_R2_F20_I30_S2169_L001_R1_001.good.fq | 2,672,666 | 397,513,894 | 100.0% | 148.7 bases | 149 bases | 98.1% |
total | 5,345,332 | 795,027,788 | 100.0% | 148.7 bases | 149 bases | 96.0% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | CP009273 | 4,631,469 | 163.6 | 2.3 | 100.0% | Escherichia coli BW25113, complete genome. |
total | 4,631,469 | 100.0% |
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.
option | limit | actual |
---|---|---|
Number of alignment pairs examined for constructing junction candidates | ≤ 100000 | 56963 |
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 threshold | 100 ≤ n ≤ 5000 | 313 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.021 |
reference sequence | pr(no read start) |
---|---|
CP009273 | 0.65097 |
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.
option | value |
---|---|
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 |
option | value |
---|---|
Mode | Consensus/Mixed Base |
Ploidy | 1 (haploid) |
Consensus mutation E-value cutoff | 10 |
Consensus frequency cutoff | 0.8 |
Consensus minimum coverage each strand | OFF |
Polymorphism E-value cutoff | 10 |
Polymorphism frequency cutoff | 0.2 |
Polymorphism minimum coverage each strand | OFF |
Polymorphism bias cutoff | OFF |
Predict indel polymorphisms | YES |
Skip indel polymorphisms in homopolymers runs of | OFF |
Skip base substitutions when they create a homopolymer flanked on each side by | OFF |
program | version |
---|---|
bowtie2 | 2.3.2 |
R | 3.4.2 |
step | start | end | elapsed |
---|---|---|---|
Read and reference sequence file input | 23:30:27 15 Jun 2018 | 23:31:34 15 Jun 2018 | 1 minute 7 seconds |
Read alignment to reference genome | 23:31:34 15 Jun 2018 | 23:36:43 15 Jun 2018 | 5 minutes 9 seconds |
Preprocessing alignments for candidate junction identification | 23:36:43 15 Jun 2018 | 23:37:38 15 Jun 2018 | 55 seconds |
Preliminary analysis of coverage distribution | 23:37:38 15 Jun 2018 | 23:40:11 15 Jun 2018 | 2 minutes 33 seconds |
Identifying junction candidates | 23:40:11 15 Jun 2018 | 23:40:53 15 Jun 2018 | 42 seconds |
Re-alignment to junction candidates | 23:40:53 15 Jun 2018 | 23:42:05 15 Jun 2018 | 1 minute 12 seconds |
Resolving alignments with junction candidates | 23:42:05 15 Jun 2018 | 23:43:44 15 Jun 2018 | 1 minute 39 seconds |
Creating BAM files | 23:43:44 15 Jun 2018 | 23:46:05 15 Jun 2018 | 2 minutes 21 seconds |
Tabulating error counts | 23:46:05 15 Jun 2018 | 23:47:10 15 Jun 2018 | 1 minute 5 seconds |
Re-calibrating base error rates | 23:47:10 15 Jun 2018 | 23:47:11 15 Jun 2018 | 1 second |
Examining read alignment evidence | 23:47:11 15 Jun 2018 | 00:00:43 16 Jun 2018 | 13 minutes 32 seconds |
Polymorphism statistics | 00:00:43 16 Jun 2018 | 00:00:43 16 Jun 2018 | 0 seconds |
Output | 00:00:43 16 Jun 2018 | 00:01:06 16 Jun 2018 | 23 seconds |
Total | 30 minutes 39 seconds |