mutation predictions | marginal predictions | summary statistics | genome diff | command line log
|
breseq version 0.26.0
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
| read file | reads | bases | passed filters | average | longest | mapped | |
|---|---|---|---|---|---|---|---|
| errors | 8Glu_S10_L001_R1_001 | 752,896 | 212,282,912 | 100.0% | 282.0 bases | 301 bases | 91.7% |
| errors | 8Glu_S10_L001_R2_001 | 752,869 | 212,494,630 | 100.0% | 282.2 bases | 301 bases | 84.8% |
| total | 1,505,765 | 424,777,542 | 100.0% | 282.1 bases | 301 bases | 88.3% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 81.4 | 3.6 | 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 | 2786 |
| 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 | 154 |
| Total length of all junction candidates (factor times the reference genome length) | ≥ 0.1 | 0.020 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.91553 |
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 | ≤ 0 |
| Number of bases that at least one read must overlap each uniquely aligned side of a predicted junction | ≥ 6 |
| option | value |
|---|---|
| Mode | Full Polymorphism |
| Ploidy | 1 (haploid) |
| Consensus mutation E-value cutoff | 10 |
| Polymorphism E-value cutoff | 2 |
| Polymorphism frequency cutoff | 0.05 |
| Polymorphism minimum coverage each strand | 2 |
| Polymorphism bias cutoff | 0.001 |
| Predict indel polymorphisms | YES |
| Skip indel polymorphisms in homopolymers runs of | ≥3 bases |
| Skip base substitutions when they create a homopolymer flanked on each side by | ≥2 bases |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 09:33:16 16 Apr 2015 | 09:33:57 16 Apr 2015 | 41 seconds |
| Read alignment to reference genome | 09:33:57 16 Apr 2015 | 09:40:43 16 Apr 2015 | 6 minutes 46 seconds |
| Preprocessing alignments for candidate junction identification | 09:40:43 16 Apr 2015 | 09:41:29 16 Apr 2015 | 46 seconds |
| Preliminary analysis of coverage distribution | 09:41:29 16 Apr 2015 | 09:43:44 16 Apr 2015 | 2 minutes 15 seconds |
| Identifying junction candidates | 09:43:44 16 Apr 2015 | 09:43:45 16 Apr 2015 | 1 second |
| Re-alignment to junction candidates | 09:43:45 16 Apr 2015 | 09:44:06 16 Apr 2015 | 21 seconds |
| Resolving alignments with junction candidates | 09:44:06 16 Apr 2015 | 09:45:17 16 Apr 2015 | 1 minute 11 seconds |
| Creating BAM files | 09:45:17 16 Apr 2015 | 09:46:41 16 Apr 2015 | 1 minute 24 seconds |
| Tabulating error counts | 09:46:41 16 Apr 2015 | 09:48:48 16 Apr 2015 | 2 minutes 7 seconds |
| Re-calibrating base error rates | 09:48:48 16 Apr 2015 | 09:48:49 16 Apr 2015 | 1 second |
| Examining read alignment evidence | 09:48:49 16 Apr 2015 | 11:27:03 16 Apr 2015 | 1 hour 38 minutes 14 seconds |
| Polymorphism statistics | 11:27:03 16 Apr 2015 | 11:27:04 16 Apr 2015 | 1 second |
| Output | 11:27:04 16 Apr 2015 | 11:27:48 16 Apr 2015 | 44 seconds |
| Total | 1 hour 54 minutes 32 seconds | ||
