mutation predictions | marginal predictions | summary statistics | genome diff | command line log
|
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 | Plate-2-BOP-1000-SUCB-ALE-1-flask-10_S41_L001_R1_001.good.fq | 200,447 | 25,329,648 | 100.0% | 126.4 bases | 149 bases | 94.9% |
| errors | Plate-2-BOP-1000-SUCB-ALE-1-flask-10_S41_L001_R2_001.good.fq | 200,447 | 25,015,019 | 100.0% | 124.8 bases | 149 bases | 97.8% |
| errors | Plate-2-BOP-1000-SUCB-ALE-1-flask-10_S41_L002_R1_001.good.fq | 160,772 | 20,223,613 | 100.0% | 125.8 bases | 149 bases | 94.3% |
| errors | Plate-2-BOP-1000-SUCB-ALE-1-flask-10_S41_L002_R2_001.good.fq | 160,772 | 19,960,179 | 100.0% | 124.2 bases | 149 bases | 97.2% |
| errors | Plate-2-BOP-1000-SUCB-ALE-1-flask-10_S41_L003_R1_001.good.fq | 181,779 | 22,893,212 | 100.0% | 125.9 bases | 149 bases | 94.6% |
| errors | Plate-2-BOP-1000-SUCB-ALE-1-flask-10_S41_L003_R2_001.good.fq | 181,779 | 22,595,805 | 100.0% | 124.3 bases | 149 bases | 97.7% |
| errors | Plate-2-BOP-1000-SUCB-ALE-1-flask-10_S41_L004_R1_001.good.fq | 157,344 | 19,729,896 | 100.0% | 125.4 bases | 149 bases | 94.4% |
| errors | Plate-2-BOP-1000-SUCB-ALE-1-flask-10_S41_L004_R2_001.good.fq | 157,344 | 19,490,200 | 100.0% | 123.9 bases | 149 bases | 97.0% |
| total | 1,400,684 | 175,237,572 | 100.0% | 125.1 bases | 149 bases | 96.0% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 35.5 | 3.6 | 100.0% | Escherichia coli str. K-12 substr. MG1655, complete genome. |
| total | 4,641,652 | 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 | 17128 |
| 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 | 202 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.013 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.87312 |
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 | 0.75 |
| 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 | 10 |
| Polymorphism frequency cutoff | 0.2 |
| Polymorphism minimum variant coverage each strand | OFF |
| 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 | OFF |
| Skip base substitutions when they create a homopolymer flanked on each side by | OFF |
| program | version |
|---|---|
| bowtie2 | 2.3.4.1 |
| R | 3.4.4 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 23:06:37 25 Feb 2020 | 23:06:58 25 Feb 2020 | 21 seconds |
| Read alignment to reference genome | 23:06:58 25 Feb 2020 | 23:09:35 25 Feb 2020 | 2 minutes 37 seconds |
| Preprocessing alignments for candidate junction identification | 23:09:35 25 Feb 2020 | 23:09:54 25 Feb 2020 | 19 seconds |
| Preliminary analysis of coverage distribution | 23:09:54 25 Feb 2020 | 23:10:32 25 Feb 2020 | 38 seconds |
| Identifying junction candidates | 23:10:32 25 Feb 2020 | 23:11:17 25 Feb 2020 | 45 seconds |
| Re-alignment to junction candidates | 23:11:17 25 Feb 2020 | 23:12:09 25 Feb 2020 | 52 seconds |
| Resolving best read alignments | 23:12:09 25 Feb 2020 | 23:12:38 25 Feb 2020 | 29 seconds |
| Creating BAM files | 23:12:38 25 Feb 2020 | 23:13:12 25 Feb 2020 | 34 seconds |
| Tabulating error counts | 23:13:12 25 Feb 2020 | 23:13:24 25 Feb 2020 | 12 seconds |
| Re-calibrating base error rates | 23:13:24 25 Feb 2020 | 23:13:27 25 Feb 2020 | 3 seconds |
| Examining read alignment evidence | 23:13:27 25 Feb 2020 | 23:16:01 25 Feb 2020 | 2 minutes 34 seconds |
| Polymorphism statistics | 23:16:01 25 Feb 2020 | 23:16:02 25 Feb 2020 | 1 second |
| Output | 23:16:02 25 Feb 2020 | 23:16:18 25 Feb 2020 | 16 seconds |
| Total | 9 minutes 41 seconds | ||
