breseq version 0.33.1 revision 8505477f25b3
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
read file | reads | bases | passed filters | average | longest | mapped | |
---|---|---|---|---|---|---|---|
errors | ALE-22_S22_L001_R1_001.good.fq | 395,850 | 57,210,189 | 100.0% | 144.5 bases | 149 bases | 93.9% |
errors | ALE-22_S22_L001_R2_001.good.fq | 395,850 | 57,068,818 | 100.0% | 144.2 bases | 149 bases | 94.1% |
errors | ALE-22_S22_L002_R1_001.good.fq | 391,862 | 56,572,145 | 100.0% | 144.4 bases | 149 bases | 95.3% |
errors | ALE-22_S22_L002_R2_001.good.fq | 391,862 | 56,460,044 | 100.0% | 144.1 bases | 149 bases | 94.4% |
errors | ALE-22_S22_L003_R1_001.good.fq | 401,325 | 57,893,538 | 100.0% | 144.3 bases | 149 bases | 95.3% |
errors | ALE-22_S22_L003_R2_001.good.fq | 401,325 | 57,756,276 | 100.0% | 143.9 bases | 149 bases | 95.1% |
errors | ALE-22_S22_L004_R1_001.good.fq | 374,350 | 54,010,555 | 100.0% | 144.3 bases | 149 bases | 95.1% |
errors | ALE-22_S22_L004_R2_001.good.fq | 374,350 | 53,906,990 | 100.0% | 144.0 bases | 149 bases | 94.0% |
total | 3,126,774 | 450,878,555 | 100.0% | 144.2 bases | 149 bases | 94.7% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_002947 | 6,181,873 | 68.5 | 2.8 | 100.0% | Pseudomonas putida KT2440 chromosome, complete genome. |
total | 6,181,873 | 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 | 72637 |
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 | 480 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.024 |
reference sequence | pr(no read start) |
---|---|
NC_002947 | 0.80757 |
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 | ≤ 0 |
Number of bases that at least one read must overlap each uniquely aligned side of a predicted junction | ≥ 6 |
option | value |
---|---|
Mode | Full Polymorphism |
Ploidy | 1 (haploid) |
Consensus mutation E-value cutoff | 10 |
Consensus frequency cutoff | 0.75 |
Consensus minimum variant coverage each strand | OFF |
Consensus minimum total coverage each strand | OFF |
Consensus minimum variant coverage | OFF |
Consensus minimum total coverage | OFF |
Polymorphism E-value cutoff | 2 |
Polymorphism frequency cutoff | 0.05 |
Polymorphism minimum variant coverage each strand | 2 |
Polymorphism minimum total coverage each strand | OFF |
Polymorphism minimum variant coverage | OFF |
Polymorphism minimum total coverage | OFF |
Polymorphism bias cutoff | OFF |
Predict indel polymorphisms | YES |
Skip indel polymorphisms in homopolymers runs of | ≥3 bases |
Skip base substitutions when they create a homopolymer flanked on each side by | ≥5 bases |
program | version |
---|---|
bowtie2 | 2.3.4.1 |
R | 3.4.4 |
step | start | end | elapsed |
---|---|---|---|
Read and reference sequence file input | 10:17:03 18 Feb 2020 | 10:17:50 18 Feb 2020 | 47 seconds |
Read alignment to reference genome | 10:17:50 18 Feb 2020 | 10:24:50 18 Feb 2020 | 7 minutes 0 seconds |
Preprocessing alignments for candidate junction identification | 10:24:50 18 Feb 2020 | 10:25:34 18 Feb 2020 | 44 seconds |
Preliminary analysis of coverage distribution | 10:25:34 18 Feb 2020 | 10:27:24 18 Feb 2020 | 1 minute 50 seconds |
Identifying junction candidates | 10:27:24 18 Feb 2020 | 10:33:52 18 Feb 2020 | 6 minutes 28 seconds |
Re-alignment to junction candidates | 10:33:52 18 Feb 2020 | 10:36:02 18 Feb 2020 | 2 minutes 10 seconds |
Resolving best read alignments | 10:36:02 18 Feb 2020 | 10:37:09 18 Feb 2020 | 1 minute 7 seconds |
Creating BAM files | 10:37:09 18 Feb 2020 | 10:38:51 18 Feb 2020 | 1 minute 42 seconds |
Tabulating error counts | 10:38:51 18 Feb 2020 | 10:39:24 18 Feb 2020 | 33 seconds |
Re-calibrating base error rates | 10:39:24 18 Feb 2020 | 10:39:27 18 Feb 2020 | 3 seconds |
Examining read alignment evidence | 10:39:27 18 Feb 2020 | 11:00:14 18 Feb 2020 | 20 minutes 47 seconds |
Polymorphism statistics | 11:00:14 18 Feb 2020 | 11:00:16 18 Feb 2020 | 2 seconds |
Output | 11:00:16 18 Feb 2020 | 11:03:44 18 Feb 2020 | 3 minutes 28 seconds |
Total | 46 minutes 41 seconds |