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-1-BOP-1000-PFKA-END-2_S26_L001_R1_001.good.fq | 432,415 | 60,846,782 | 100.0% | 140.7 bases | 149 bases | 98.2% |
| errors | Plate-1-BOP-1000-PFKA-END-2_S26_L001_R2_001.good.fq | 432,415 | 60,681,593 | 100.0% | 140.3 bases | 149 bases | 98.3% |
| errors | Plate-1-BOP-1000-PFKA-END-2_S26_L002_R1_001.good.fq | 399,288 | 56,271,362 | 100.0% | 140.9 bases | 149 bases | 98.3% |
| errors | Plate-1-BOP-1000-PFKA-END-2_S26_L002_R2_001.good.fq | 399,288 | 56,137,804 | 100.0% | 140.6 bases | 149 bases | 97.9% |
| errors | Plate-1-BOP-1000-PFKA-END-2_S26_L003_R1_001.good.fq | 421,226 | 59,255,098 | 100.0% | 140.7 bases | 149 bases | 98.1% |
| errors | Plate-1-BOP-1000-PFKA-END-2_S26_L003_R2_001.good.fq | 421,226 | 59,095,928 | 100.0% | 140.3 bases | 149 bases | 98.1% |
| errors | Plate-1-BOP-1000-PFKA-END-2_S26_L004_R1_001.good.fq | 432,263 | 60,812,000 | 100.0% | 140.7 bases | 149 bases | 98.3% |
| errors | Plate-1-BOP-1000-PFKA-END-2_S26_L004_R2_001.good.fq | 432,263 | 60,678,571 | 100.0% | 140.4 bases | 149 bases | 98.0% |
| total | 3,370,384 | 473,779,138 | 100.0% | 140.6 bases | 149 bases | 98.1% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 107.5 | 7.6 | 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 | 13840 |
| 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 | 13 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.001 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.73546 |
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 | 2.2.6 |
| R | 3.4.4 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 20:29:09 10 Sep 2020 | 20:30:00 10 Sep 2020 | 51 seconds |
| Read alignment to reference genome | 20:30:01 10 Sep 2020 | 20:36:22 10 Sep 2020 | 6 minutes 21 seconds |
| Preprocessing alignments for candidate junction identification | 20:36:22 10 Sep 2020 | 20:37:14 10 Sep 2020 | 52 seconds |
| Preliminary analysis of coverage distribution | 20:37:14 10 Sep 2020 | 20:39:12 10 Sep 2020 | 1 minute 58 seconds |
| Identifying junction candidates | 20:39:12 10 Sep 2020 | 20:39:22 10 Sep 2020 | 10 seconds |
| Re-alignment to junction candidates | 20:39:22 10 Sep 2020 | 20:41:13 10 Sep 2020 | 1 minute 51 seconds |
| Resolving best read alignments | 20:41:13 10 Sep 2020 | 20:42:33 10 Sep 2020 | 1 minute 20 seconds |
| Creating BAM files | 20:42:33 10 Sep 2020 | 20:44:22 10 Sep 2020 | 1 minute 49 seconds |
| Tabulating error counts | 20:44:22 10 Sep 2020 | 20:44:58 10 Sep 2020 | 36 seconds |
| Re-calibrating base error rates | 20:44:58 10 Sep 2020 | 20:45:01 10 Sep 2020 | 3 seconds |
| Examining read alignment evidence | 20:45:01 10 Sep 2020 | 20:52:21 10 Sep 2020 | 7 minutes 20 seconds |
| Polymorphism statistics | 20:52:21 10 Sep 2020 | 20:52:22 10 Sep 2020 | 1 second |
| Output | 20:52:22 10 Sep 2020 | 20:52:33 10 Sep 2020 | 11 seconds |
| Total | 23 minutes 23 seconds | ||
