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 | Plate-3-BOP-1000-ACNB-END-1_S50_L001_R1_001.good.fq | 376,096 | 53,384,568 | 100.0% | 141.9 bases | 149 bases | 96.3% |
| errors | Plate-3-BOP-1000-ACNB-END-1_S50_L001_R2_001.good.fq | 376,096 | 52,971,375 | 100.0% | 140.8 bases | 149 bases | 97.5% |
| errors | Plate-3-BOP-1000-ACNB-END-1_S50_L002_R1_001.good.fq | 344,424 | 48,895,433 | 100.0% | 142.0 bases | 149 bases | 96.5% |
| errors | Plate-3-BOP-1000-ACNB-END-1_S50_L002_R2_001.good.fq | 344,424 | 48,554,791 | 100.0% | 141.0 bases | 149 bases | 97.3% |
| errors | Plate-3-BOP-1000-ACNB-END-1_S50_L003_R1_001.good.fq | 365,418 | 51,829,710 | 100.0% | 141.8 bases | 149 bases | 96.2% |
| errors | Plate-3-BOP-1000-ACNB-END-1_S50_L003_R2_001.good.fq | 365,418 | 51,439,969 | 100.0% | 140.8 bases | 149 bases | 97.3% |
| errors | Plate-3-BOP-1000-ACNB-END-1_S50_L004_R1_001.good.fq | 369,439 | 52,402,470 | 100.0% | 141.8 bases | 149 bases | 96.4% |
| errors | Plate-3-BOP-1000-ACNB-END-1_S50_L004_R2_001.good.fq | 369,439 | 52,007,538 | 100.0% | 140.8 bases | 149 bases | 97.5% |
| total | 2,910,754 | 411,485,854 | 100.0% | 141.4 bases | 149 bases | 96.9% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 84.3 | 3.9 | 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 | 22442 |
| 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 | 47 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.003 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.76778 |
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 | ≤ 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 | 2.2.6 |
| R | 3.4.4 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 10:33:59 06 Apr 2022 | 10:34:52 06 Apr 2022 | 53 seconds |
| Read alignment to reference genome | 10:34:52 06 Apr 2022 | 10:40:46 06 Apr 2022 | 5 minutes 54 seconds |
| Preprocessing alignments for candidate junction identification | 10:40:46 06 Apr 2022 | 10:41:23 06 Apr 2022 | 37 seconds |
| Preliminary analysis of coverage distribution | 10:41:23 06 Apr 2022 | 10:43:06 06 Apr 2022 | 1 minute 43 seconds |
| Identifying junction candidates | 10:43:06 06 Apr 2022 | 10:43:27 06 Apr 2022 | 21 seconds |
| Re-alignment to junction candidates | 10:43:27 06 Apr 2022 | 10:44:49 06 Apr 2022 | 1 minute 22 seconds |
| Resolving best read alignments | 10:44:49 06 Apr 2022 | 10:45:42 06 Apr 2022 | 53 seconds |
| Creating BAM files | 10:45:42 06 Apr 2022 | 10:47:14 06 Apr 2022 | 1 minute 32 seconds |
| Tabulating error counts | 10:47:14 06 Apr 2022 | 10:47:52 06 Apr 2022 | 38 seconds |
| Re-calibrating base error rates | 10:47:52 06 Apr 2022 | 10:47:55 06 Apr 2022 | 3 seconds |
| Examining read alignment evidence | 10:47:55 06 Apr 2022 | 11:14:49 06 Apr 2022 | 26 minutes 54 seconds |
| Polymorphism statistics | 11:14:49 06 Apr 2022 | 11:14:50 06 Apr 2022 | 1 second |
| Output | 11:14:50 06 Apr 2022 | 11:15:08 06 Apr 2022 | 18 seconds |
| Total | 41 minutes 9 seconds | ||
