mutation predictions | marginal predictions | summary statistics | genome diff | command line log
|
breseq version 0.29.0 revision 8f9c342918e4
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
| read file | reads | bases | passed filters | average | longest | mapped | |
|---|---|---|---|---|---|---|---|
| errors | BOP27Reseq_S1_L001_R1 | 5,978,523 | 980,052,088 | 100.0% | 163.9 bases | 251 bases | 99.0% |
| errors | BOP27Reseq_S1_L001_R2 | 5,977,520 | 980,235,110 | 100.0% | 164.0 bases | 251 bases | 98.7% |
| total | 11,956,043 | 1,960,287,198 | 100.0% | 164.0 bases | 251 bases | 98.9% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 422.4 | 11.9 | 98.3% | 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 | 6340 |
| 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 | 772 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.085 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.62484 |
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 | 19:42:02 15 Jan 2017 | 19:45:04 15 Jan 2017 | 3 minutes 2 seconds |
| Read alignment to reference genome | 19:45:05 15 Jan 2017 | 19:55:54 15 Jan 2017 | 10 minutes 49 seconds |
| Preprocessing alignments for candidate junction identification | 19:55:54 15 Jan 2017 | 20:01:31 15 Jan 2017 | 5 minutes 37 seconds |
| Preliminary analysis of coverage distribution | 20:01:31 15 Jan 2017 | 20:10:22 15 Jan 2017 | 8 minutes 51 seconds |
| Identifying junction candidates | 20:10:22 15 Jan 2017 | 20:10:50 15 Jan 2017 | 28 seconds |
| Re-alignment to junction candidates | 20:10:50 15 Jan 2017 | 20:13:52 15 Jan 2017 | 3 minutes 2 seconds |
| Resolving alignments with junction candidates | 20:13:52 15 Jan 2017 | 20:25:39 15 Jan 2017 | 11 minutes 47 seconds |
| Creating BAM files | 20:25:39 15 Jan 2017 | 20:33:08 15 Jan 2017 | 7 minutes 29 seconds |
| Tabulating error counts | 20:33:08 15 Jan 2017 | 20:43:39 15 Jan 2017 | 10 minutes 31 seconds |
| Re-calibrating base error rates | 20:43:39 15 Jan 2017 | 20:43:40 15 Jan 2017 | 1 second |
| Examining read alignment evidence | 20:43:40 15 Jan 2017 | 21:52:17 15 Jan 2017 | 1 hour 8 minutes 37 seconds |
| Polymorphism statistics | 21:52:17 15 Jan 2017 | 21:52:27 15 Jan 2017 | 10 seconds |
| Output | 21:52:27 15 Jan 2017 | 21:53:27 15 Jan 2017 | 1 minute 0 seconds |
| Total | 2 hours 11 minutes 24 seconds | ||
