mutation predictions | marginal predictions | summary statistics | genome diff | command line log
|
breseq version 0.35.4 revision f352f80f4bc9
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
| read file | reads | bases | passed filters | average | longest | mapped | |
|---|---|---|---|---|---|---|---|
| errors | Putida-Van-ACB143-A16-F16-I1-R1_S79_L001_R1_001.good.fq | 381,862 | 49,773,457 | 100.0% | 130.3 bases | 137 bases | 96.0% |
| errors | Putida-Van-ACB143-A16-F16-I1-R1_S79_L001_R2_001.good.fq | 381,862 | 49,773,457 | 100.0% | 130.3 bases | 137 bases | 95.0% |
| errors | Putida-Van-ACB143-A16-F16-I1-R1_S79_L002_R1_001.good.fq | 369,711 | 48,312,645 | 100.0% | 130.7 bases | 137 bases | 96.5% |
| errors | Putida-Van-ACB143-A16-F16-I1-R1_S79_L002_R2_001.good.fq | 369,711 | 48,312,645 | 100.0% | 130.7 bases | 137 bases | 95.4% |
| errors | Putida-Van-ACB143-A16-F16-I1-R1_S79_L003_R1_001.good.fq | 391,196 | 51,150,046 | 100.0% | 130.8 bases | 137 bases | 96.6% |
| errors | Putida-Van-ACB143-A16-F16-I1-R1_S79_L003_R2_001.good.fq | 391,196 | 51,150,046 | 100.0% | 130.8 bases | 137 bases | 95.4% |
| errors | Putida-Van-ACB143-A16-F16-I1-R1_S79_L004_R1_001.good.fq | 384,905 | 50,298,610 | 100.0% | 130.7 bases | 137 bases | 96.5% |
| errors | Putida-Van-ACB143-A16-F16-I1-R1_S79_L004_R2_001.good.fq | 384,905 | 50,298,610 | 100.0% | 130.7 bases | 137 bases | 95.3% |
| total | 3,055,348 | 399,069,516 | 100.0% | 130.6 bases | 137 bases | 95.8% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | ACB143 | 6,188,635 | 62.1 | 2.6 | 100.0% | tig00000001_arrow. |
| total | 6,188,635 | 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 | 1835 |
| 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 | 100 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.005 |
| reference sequence | pr(no read start) |
|---|---|
| ACB143 | 0.85216 |
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 |
| Minimum probablilty assigned that no mapped read will start at a given position and strand for junction prediction | 0.1 |
| Junction allow suboptimal matches | FALSE |
| 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 | 2.2.6 |
| R | 3.4.4 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 11:15:35 28 Apr 2023 | 11:16:27 28 Apr 2023 | 52 seconds |
| Read alignment to reference genome | 11:16:27 28 Apr 2023 | 11:23:18 28 Apr 2023 | 6 minutes 51 seconds |
| Preprocessing alignments for candidate junction identification | 11:23:18 28 Apr 2023 | 11:23:57 28 Apr 2023 | 39 seconds |
| Preliminary analysis of coverage distribution | 11:23:57 28 Apr 2023 | 11:25:44 28 Apr 2023 | 1 minute 47 seconds |
| Identifying junction candidates | 11:25:44 28 Apr 2023 | 11:25:44 28 Apr 2023 | 0 seconds |
| Re-alignment to junction candidates | 11:25:44 28 Apr 2023 | 11:27:20 28 Apr 2023 | 1 minute 36 seconds |
| Resolving best read alignments | 11:27:20 28 Apr 2023 | 11:28:13 28 Apr 2023 | 53 seconds |
| Creating BAM files | 11:28:13 28 Apr 2023 | 11:29:49 28 Apr 2023 | 1 minute 36 seconds |
| Tabulating error counts | 11:29:49 28 Apr 2023 | 11:30:24 28 Apr 2023 | 35 seconds |
| Re-calibrating base error rates | 11:30:24 28 Apr 2023 | 11:30:27 28 Apr 2023 | 3 seconds |
| Examining read alignment evidence | 11:30:27 28 Apr 2023 | 11:37:44 28 Apr 2023 | 7 minutes 17 seconds |
| Polymorphism statistics | 11:37:44 28 Apr 2023 | 11:37:45 28 Apr 2023 | 1 second |
| Output | 11:37:45 28 Apr 2023 | 11:38:03 28 Apr 2023 | 18 seconds |
| Total | 22 minutes 28 seconds | ||
