mutation predictions | marginal predictions | summary statistics | genome diff | command line log
|
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 | A9_F044_R2_F34_I0_S2191_L001_R2_001.good.fq | 358,758 | 53,417,731 | 100.0% | 148.9 bases | 149 bases | 93.2% |
| errors | A9_F044_R2_F34_I0_S2191_L001_R1_001.good.fq | 358,758 | 53,417,731 | 100.0% | 148.9 bases | 149 bases | 98.9% |
| total | 717,516 | 106,835,462 | 100.0% | 148.9 bases | 149 bases | 96.1% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | CP009273 | 4,631,469 | 22.0 | 1.5 | 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 | 2600 |
| Coverage evenness (position-hash) score of junction candidates | ≥ 2 | ≥ 2 |
| Test this many junction candidates (n). May be smaller if not enough passed the coverage evenness threshold | 100 ≤ n ≤ 5000 | 46 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.003 |
| reference sequence | pr(no read start) |
|---|---|
| CP009273 | 0.93822 |
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 | OFF |
| Consensus minimum coverage each strand | OFF |
| Polymorphism E-value cutoff | 2 |
| Polymorphism frequency cutoff | 0.025 |
| Polymorphism minimum coverage each strand | 2 |
| 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 | 2.3.2 |
| R | 3.4.2 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 17:42:22 15 Jun 2018 | 17:42:32 15 Jun 2018 | 10 seconds |
| Read alignment to reference genome | 17:42:32 15 Jun 2018 | 17:43:16 15 Jun 2018 | 44 seconds |
| Preprocessing alignments for candidate junction identification | 17:43:16 15 Jun 2018 | 17:43:23 15 Jun 2018 | 7 seconds |
| Preliminary analysis of coverage distribution | 17:43:23 15 Jun 2018 | 17:43:44 15 Jun 2018 | 21 seconds |
| Identifying junction candidates | 17:43:44 15 Jun 2018 | 17:43:44 15 Jun 2018 | 0 seconds |
| Re-alignment to junction candidates | 17:43:44 15 Jun 2018 | 17:43:52 15 Jun 2018 | 8 seconds |
| Resolving alignments with junction candidates | 17:43:52 15 Jun 2018 | 17:44:04 15 Jun 2018 | 12 seconds |
| Creating BAM files | 17:44:04 15 Jun 2018 | 17:44:23 15 Jun 2018 | 19 seconds |
| Tabulating error counts | 17:44:23 15 Jun 2018 | 17:44:31 15 Jun 2018 | 8 seconds |
| Re-calibrating base error rates | 17:44:31 15 Jun 2018 | 17:44:32 15 Jun 2018 | 1 second |
| Examining read alignment evidence | 17:44:32 15 Jun 2018 | 17:51:08 15 Jun 2018 | 6 minutes 36 seconds |
| Polymorphism statistics | 17:51:08 15 Jun 2018 | 17:51:08 15 Jun 2018 | 0 seconds |
| Output | 17:51:08 15 Jun 2018 | 17:51:14 15 Jun 2018 | 6 seconds |
| Total | 8 minutes 52 seconds | ||
