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-2-BOP-1000-ACEF-ALE-1-flask-47_S10_L001_R1_001.good.fq | 192,034 | 25,319,609 | 100.0% | 131.8 bases | 149 bases | 96.1% |
| errors | Plate-2-BOP-1000-ACEF-ALE-1-flask-47_S10_L001_R2_001.good.fq | 192,034 | 25,084,915 | 100.0% | 130.6 bases | 149 bases | 98.3% |
| errors | Plate-2-BOP-1000-ACEF-ALE-1-flask-47_S10_L002_R1_001.good.fq | 153,983 | 20,229,282 | 100.0% | 131.4 bases | 149 bases | 95.7% |
| errors | Plate-2-BOP-1000-ACEF-ALE-1-flask-47_S10_L002_R2_001.good.fq | 153,983 | 20,031,406 | 100.0% | 130.1 bases | 149 bases | 97.7% |
| errors | Plate-2-BOP-1000-ACEF-ALE-1-flask-47_S10_L003_R1_001.good.fq | 173,392 | 22,785,140 | 100.0% | 131.4 bases | 149 bases | 96.0% |
| errors | Plate-2-BOP-1000-ACEF-ALE-1-flask-47_S10_L003_R2_001.good.fq | 173,392 | 22,569,147 | 100.0% | 130.2 bases | 149 bases | 98.1% |
| errors | Plate-2-BOP-1000-ACEF-ALE-1-flask-47_S10_L004_R1_001.good.fq | 150,295 | 19,721,171 | 100.0% | 131.2 bases | 149 bases | 95.6% |
| errors | Plate-2-BOP-1000-ACEF-ALE-1-flask-47_S10_L004_R2_001.good.fq | 150,295 | 19,531,150 | 100.0% | 130.0 bases | 149 bases | 97.5% |
| total | 1,339,408 | 175,271,820 | 100.0% | 130.9 bases | 149 bases | 96.9% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 36.8 | 2.1 | 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 | 10843 |
| 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 | 75 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.005 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.87620 |
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 | 2.3.4.1 |
| R | 3.4.4 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 04:53:15 29 Feb 2020 | 04:53:35 29 Feb 2020 | 20 seconds |
| Read alignment to reference genome | 04:53:35 29 Feb 2020 | 04:56:08 29 Feb 2020 | 2 minutes 33 seconds |
| Preprocessing alignments for candidate junction identification | 04:56:08 29 Feb 2020 | 04:56:27 29 Feb 2020 | 19 seconds |
| Preliminary analysis of coverage distribution | 04:56:27 29 Feb 2020 | 04:57:05 29 Feb 2020 | 38 seconds |
| Identifying junction candidates | 04:57:05 29 Feb 2020 | 04:57:30 29 Feb 2020 | 25 seconds |
| Re-alignment to junction candidates | 04:57:30 29 Feb 2020 | 04:58:18 29 Feb 2020 | 48 seconds |
| Resolving best read alignments | 04:58:19 29 Feb 2020 | 04:58:47 29 Feb 2020 | 28 seconds |
| Creating BAM files | 04:58:47 29 Feb 2020 | 04:59:21 29 Feb 2020 | 34 seconds |
| Tabulating error counts | 04:59:21 29 Feb 2020 | 04:59:34 29 Feb 2020 | 13 seconds |
| Re-calibrating base error rates | 04:59:34 29 Feb 2020 | 04:59:37 29 Feb 2020 | 3 seconds |
| Examining read alignment evidence | 04:59:37 29 Feb 2020 | 05:02:14 29 Feb 2020 | 2 minutes 37 seconds |
| Polymorphism statistics | 05:02:14 29 Feb 2020 | 05:02:14 29 Feb 2020 | 0 seconds |
| Output | 05:02:14 29 Feb 2020 | 05:02:27 29 Feb 2020 | 13 seconds |
| Total | 9 minutes 11 seconds | ||
