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 | pgi-2_S1_L001_R2_001 | 913,530 | 265,416,379 | 100.0% | 290.5 bases | 301 bases | 84.4% |
| errors | pgi-2_S1_L001_R1_001 | 913,565 | 263,980,379 | 100.0% | 289.0 bases | 301 bases | 99.3% |
| total | 1,827,095 | 529,396,758 | 100.0% | 289.7 bases | 301 bases | 91.9% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 109.8 | 4.4 | 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 | 2054 |
| 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 | 155 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.020 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.89665 |
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 | 21:15:35 17 Jun 2016 | 21:16:22 17 Jun 2016 | 47 seconds |
| Read alignment to reference genome | 21:16:22 17 Jun 2016 | 21:20:56 17 Jun 2016 | 4 minutes 34 seconds |
| Preprocessing alignments for candidate junction identification | 21:20:56 17 Jun 2016 | 21:21:53 17 Jun 2016 | 57 seconds |
| Preliminary analysis of coverage distribution | 21:21:53 17 Jun 2016 | 21:24:33 17 Jun 2016 | 2 minutes 40 seconds |
| Identifying junction candidates | 21:24:33 17 Jun 2016 | 21:24:34 17 Jun 2016 | 1 second |
| Re-alignment to junction candidates | 21:24:34 17 Jun 2016 | 21:25:02 17 Jun 2016 | 28 seconds |
| Resolving alignments with junction candidates | 21:25:02 17 Jun 2016 | 21:27:14 17 Jun 2016 | 2 minutes 12 seconds |
| Creating BAM files | 21:27:14 17 Jun 2016 | 21:28:49 17 Jun 2016 | 1 minute 35 seconds |
| Tabulating error counts | 21:28:49 17 Jun 2016 | 21:31:30 17 Jun 2016 | 2 minutes 41 seconds |
| Re-calibrating base error rates | 21:31:30 17 Jun 2016 | 21:31:31 17 Jun 2016 | 1 second |
| Examining read alignment evidence | 21:31:31 17 Jun 2016 | 21:51:32 17 Jun 2016 | 20 minutes 1 second |
| Polymorphism statistics | 21:51:32 17 Jun 2016 | 21:51:32 17 Jun 2016 | 0 seconds |
| Output | 21:51:32 17 Jun 2016 | 21:52:24 17 Jun 2016 | 52 seconds |
| Total | 36 minutes 49 seconds | ||
