mutation predictions | marginal predictions | summary statistics | genome diff | command line log
|
breseq version 0.27.1 revision 87c22d663cc3
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
| read file | reads | bases | passed filters | average | longest | mapped | |
|---|---|---|---|---|---|---|---|
| errors | Sample5_S5_L001_R1_001 | 1,625,234 | 242,639,495 | 100.0% | 149.3 bases | 151 bases | 99.3% |
| errors | Sample5_S5_L001_R2_001 | 1,624,399 | 242,515,142 | 99.9% | 149.3 bases | 151 bases | 98.2% |
| total | 3,249,633 | 485,154,637 | 99.9% | 149.3 bases | 151 bases | 98.8% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 104.0 | 2.9 | 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 | 21319 |
| 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 | 569 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.038 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.80859 |
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 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 09:49:32 20 Apr 2016 | 09:50:33 20 Apr 2016 | 1 minute 1 second |
| Read alignment to reference genome | 09:50:33 20 Apr 2016 | 09:53:53 20 Apr 2016 | 3 minutes 20 seconds |
| Preprocessing alignments for candidate junction identification | 09:53:53 20 Apr 2016 | 09:55:18 20 Apr 2016 | 1 minute 25 seconds |
| Preliminary analysis of coverage distribution | 09:55:18 20 Apr 2016 | 09:59:08 20 Apr 2016 | 3 minutes 50 seconds |
| Identifying junction candidates | 09:59:08 20 Apr 2016 | 09:59:11 20 Apr 2016 | 3 seconds |
| Re-alignment to junction candidates | 09:59:11 20 Apr 2016 | 09:59:58 20 Apr 2016 | 47 seconds |
| Resolving alignments with junction candidates | 09:59:58 20 Apr 2016 | 10:02:59 20 Apr 2016 | 3 minutes 1 second |
| Creating BAM files | 10:02:59 20 Apr 2016 | 10:05:22 20 Apr 2016 | 2 minutes 23 seconds |
| Tabulating error counts | 10:05:22 20 Apr 2016 | 10:08:12 20 Apr 2016 | 2 minutes 50 seconds |
| Re-calibrating base error rates | 10:08:12 20 Apr 2016 | 10:08:13 20 Apr 2016 | 1 second |
| Examining read alignment evidence | 10:08:13 20 Apr 2016 | 10:36:44 20 Apr 2016 | 28 minutes 31 seconds |
| Polymorphism statistics | 10:36:44 20 Apr 2016 | 10:36:46 20 Apr 2016 | 2 seconds |
| Output | 10:36:46 20 Apr 2016 | 10:37:57 20 Apr 2016 | 1 minute 11 seconds |
| Total | 48 minutes 25 seconds | ||
