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 | A10_F030_R1_F18_I40_S2168_L001_R1_001.good.fq | 915,565 | 136,419,185 | 100.0% | 149.0 bases | 149 bases | 98.7% |
| errors | A10_F030_R1_F18_I40_S2168_L001_R2_001.good.fq | 842,269 | 120,444,467 | 100.0% | 143.0 bases | 143 bases | 98.0% |
| total | 1,757,834 | 256,863,652 | 100.0% | 146.1 bases | 149 bases | 98.4% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | CP009273 | 4,631,469 | 54.2 | 1.8 | 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 | 9295 |
| 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 | 163 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.011 |
| reference sequence | pr(no read start) |
|---|---|
| CP009273 | 0.85233 |
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 | 00:56:07 16 Jun 2018 | 00:56:34 16 Jun 2018 | 27 seconds |
| Read alignment to reference genome | 00:56:34 16 Jun 2018 | 00:58:25 16 Jun 2018 | 1 minute 51 seconds |
| Preprocessing alignments for candidate junction identification | 00:58:25 16 Jun 2018 | 00:58:50 16 Jun 2018 | 25 seconds |
| Preliminary analysis of coverage distribution | 00:58:51 16 Jun 2018 | 00:59:43 16 Jun 2018 | 52 seconds |
| Identifying junction candidates | 00:59:43 16 Jun 2018 | 00:59:44 16 Jun 2018 | 1 second |
| Re-alignment to junction candidates | 00:59:44 16 Jun 2018 | 01:00:10 16 Jun 2018 | 26 seconds |
| Resolving alignments with junction candidates | 01:00:10 16 Jun 2018 | 01:00:46 16 Jun 2018 | 36 seconds |
| Creating BAM files | 01:00:46 16 Jun 2018 | 01:01:32 16 Jun 2018 | 46 seconds |
| Tabulating error counts | 01:01:32 16 Jun 2018 | 01:01:52 16 Jun 2018 | 20 seconds |
| Re-calibrating base error rates | 01:01:52 16 Jun 2018 | 01:01:53 16 Jun 2018 | 1 second |
| Examining read alignment evidence | 01:01:53 16 Jun 2018 | 01:06:12 16 Jun 2018 | 4 minutes 19 seconds |
| Polymorphism statistics | 01:06:12 16 Jun 2018 | 01:06:12 16 Jun 2018 | 0 seconds |
| Output | 01:06:12 16 Jun 2018 | 01:06:20 16 Jun 2018 | 8 seconds |
| Total | 10 minutes 12 seconds | ||
