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 | HM2_S12_L001_R2_001 | 1,453,572 | 218,697,123 | 100.0% | 150.5 bases | 151 bases | 96.5% |
| errors | HM2_S12_L001_R1_001 | 1,453,568 | 218,689,020 | 100.0% | 150.4 bases | 151 bases | 99.7% |
| total | 2,907,140 | 437,386,143 | 100.0% | 150.5 bases | 151 bases | 98.1% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 91.9 | 2.4 | 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 | 6146 |
| 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 | 425 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.028 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.75601 |
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 | 21:59:50 20 Feb 2016 | 22:00:30 20 Feb 2016 | 40 seconds |
| Read alignment to reference genome | 22:00:30 20 Feb 2016 | 22:02:09 20 Feb 2016 | 1 minute 39 seconds |
| Preprocessing alignments for candidate junction identification | 22:02:09 20 Feb 2016 | 22:03:08 20 Feb 2016 | 59 seconds |
| Preliminary analysis of coverage distribution | 22:03:08 20 Feb 2016 | 22:05:46 20 Feb 2016 | 2 minutes 38 seconds |
| Identifying junction candidates | 22:05:46 20 Feb 2016 | 22:05:46 20 Feb 2016 | 0 seconds |
| Re-alignment to junction candidates | 22:05:46 20 Feb 2016 | 22:06:10 20 Feb 2016 | 24 seconds |
| Resolving alignments with junction candidates | 22:06:10 20 Feb 2016 | 22:08:17 20 Feb 2016 | 2 minutes 7 seconds |
| Creating BAM files | 22:08:17 20 Feb 2016 | 22:10:00 20 Feb 2016 | 1 minute 43 seconds |
| Tabulating error counts | 22:10:00 20 Feb 2016 | 22:12:18 20 Feb 2016 | 2 minutes 18 seconds |
| Re-calibrating base error rates | 22:12:18 20 Feb 2016 | 22:12:19 20 Feb 2016 | 1 second |
| Examining read alignment evidence | 22:12:19 20 Feb 2016 | 22:27:50 20 Feb 2016 | 15 minutes 31 seconds |
| Polymorphism statistics | 22:27:50 20 Feb 2016 | 22:27:51 20 Feb 2016 | 1 second |
| Output | 22:27:51 20 Feb 2016 | 22:28:26 20 Feb 2016 | 35 seconds |
| Total | 28 minutes 36 seconds | ||
