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 | gctrim-C13-Redo-3-133_S3_L001_R2_001 | 2,455,715 | 554,722,770 | 100.0% | 225.9 bases | 251 bases | 91.4% |
| errors | gctrim-C13-Redo-3-133_S3_L001_R1_001 | 2,455,947 | 548,818,995 | 100.0% | 223.5 bases | 251 bases | 99.2% |
| total | 4,911,662 | 1,103,541,765 | 100.0% | 224.7 bases | 251 bases | 95.3% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 228.9 | 8.7 | 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 | 8894 |
| 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 | 866 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.095 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.75012 |
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 | 06:56:27 26 Jun 2016 | 06:58:06 26 Jun 2016 | 1 minute 39 seconds |
| Read alignment to reference genome | 06:58:06 26 Jun 2016 | 07:03:36 26 Jun 2016 | 5 minutes 30 seconds |
| Preprocessing alignments for candidate junction identification | 07:03:36 26 Jun 2016 | 07:05:39 26 Jun 2016 | 2 minutes 3 seconds |
| Preliminary analysis of coverage distribution | 07:05:39 26 Jun 2016 | 07:11:30 26 Jun 2016 | 5 minutes 51 seconds |
| Identifying junction candidates | 07:11:30 26 Jun 2016 | 07:11:32 26 Jun 2016 | 2 seconds |
| Re-alignment to junction candidates | 07:11:32 26 Jun 2016 | 07:13:08 26 Jun 2016 | 1 minute 36 seconds |
| Resolving alignments with junction candidates | 07:13:08 26 Jun 2016 | 07:18:23 26 Jun 2016 | 5 minutes 15 seconds |
| Creating BAM files | 07:18:23 26 Jun 2016 | 07:21:59 26 Jun 2016 | 3 minutes 36 seconds |
| Tabulating error counts | 07:21:59 26 Jun 2016 | 07:27:34 26 Jun 2016 | 5 minutes 35 seconds |
| Re-calibrating base error rates | 07:27:34 26 Jun 2016 | 07:27:35 26 Jun 2016 | 1 second |
| Examining read alignment evidence | 07:27:35 26 Jun 2016 | 08:08:12 26 Jun 2016 | 40 minutes 37 seconds |
| Polymorphism statistics | 08:08:12 26 Jun 2016 | 08:08:12 26 Jun 2016 | 0 seconds |
| Output | 08:08:12 26 Jun 2016 | 08:09:08 26 Jun 2016 | 56 seconds |
| Total | 1 hour 12 minutes 41 seconds | ||
