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 | qtrim-COUM8-6_S20_L001_R2_001 | 397,344 | 59,614,297 | 100.0% | 150.0 bases | 151 bases | 95.7% |
| errors | qtrim-COUM8-6_S20_L001_R1_001 | 397,491 | 59,795,741 | 100.0% | 150.4 bases | 151 bases | 99.5% |
| total | 794,835 | 119,410,038 | 100.0% | 150.2 bases | 151 bases | 97.6% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 25.2 | 1.2 | 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 | 162 |
| 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 | 13 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.001 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.92250 |
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 | 10:06:40 03 Jan 2017 | 10:06:53 03 Jan 2017 | 13 seconds |
| Read alignment to reference genome | 10:06:54 03 Jan 2017 | 10:08:30 03 Jan 2017 | 1 minute 36 seconds |
| Preprocessing alignments for candidate junction identification | 10:08:30 03 Jan 2017 | 10:08:49 03 Jan 2017 | 19 seconds |
| Preliminary analysis of coverage distribution | 10:08:49 03 Jan 2017 | 10:09:29 03 Jan 2017 | 40 seconds |
| Identifying junction candidates | 10:09:29 03 Jan 2017 | 10:09:29 03 Jan 2017 | 0 seconds |
| Re-alignment to junction candidates | 10:09:29 03 Jan 2017 | 10:09:49 03 Jan 2017 | 20 seconds |
| Resolving alignments with junction candidates | 10:09:49 03 Jan 2017 | 10:10:23 03 Jan 2017 | 34 seconds |
| Creating BAM files | 10:10:23 03 Jan 2017 | 10:10:48 03 Jan 2017 | 25 seconds |
| Tabulating error counts | 10:10:48 03 Jan 2017 | 10:11:20 03 Jan 2017 | 32 seconds |
| Re-calibrating base error rates | 10:11:20 03 Jan 2017 | 10:11:20 03 Jan 2017 | 0 seconds |
| Examining read alignment evidence | 10:11:20 03 Jan 2017 | 10:16:19 03 Jan 2017 | 4 minutes 59 seconds |
| Polymorphism statistics | 10:16:19 03 Jan 2017 | 10:16:19 03 Jan 2017 | 0 seconds |
| Output | 10:16:19 03 Jan 2017 | 10:16:32 03 Jan 2017 | 13 seconds |
| Total | 9 minutes 51 seconds | ||
