mutation predictions | marginal predictions | summary statistics | genome diff | command line log
|
breseq version 0.25c
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
| read file | reads | bases | passed filters | average | longest | mapped | |
|---|---|---|---|---|---|---|---|
| errors | 4_D28_ATGTCA_L002_R1_001 | 15,213,647 | 1,536,578,347 | 100.0% | 101.0 bases | 101 bases | 71.1% |
| total | 15,213,647 | 1,536,578,347 | 100.0% | 101.0 bases | 101 bases | 71.1% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_007779 | 4,646,332 | 243.0 | 1.7 | 100.0% | Escherichia coli str. K-12 substr. W3110, complete genome. |
| total | 4,646,332 | 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 | 81594 |
| 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 | 123 |
| Total length of all junction candidates (factor times the reference genome length) | ≥ 0.1 | 0.005 |
| reference sequence | pr(no read start) |
|---|---|
| NC_007779 | 0.34548 |
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 | OFF |
| 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 | 09:04:29 04 Mar 2015 | 09:06:36 04 Mar 2015 | 2 minutes 7 seconds |
| Read alignment to reference genome | 09:06:36 04 Mar 2015 | 09:13:59 04 Mar 2015 | 7 minutes 23 seconds |
| Preprocessing alignments for candidate junction identification | 09:13:59 04 Mar 2015 | 09:17:15 04 Mar 2015 | 3 minutes 16 seconds |
| Preliminary analysis of coverage distribution | 09:17:15 04 Mar 2015 | 09:24:33 04 Mar 2015 | 7 minutes 18 seconds |
| Identifying junction candidates | 09:24:33 04 Mar 2015 | 09:24:37 04 Mar 2015 | 4 seconds |
| Re-alignment to junction candidates | 09:24:37 04 Mar 2015 | 09:26:12 04 Mar 2015 | 1 minute 35 seconds |
| Resolving alignments with junction candidates | 09:26:12 04 Mar 2015 | 09:31:08 04 Mar 2015 | 4 minutes 56 seconds |
| Creating BAM files | 09:31:08 04 Mar 2015 | 09:37:46 04 Mar 2015 | 6 minutes 38 seconds |
| Tabulating error counts | 09:37:46 04 Mar 2015 | 09:39:55 04 Mar 2015 | 2 minutes 9 seconds |
| Re-calibrating base error rates | 09:39:55 04 Mar 2015 | 09:39:56 04 Mar 2015 | 1 second |
| Examining read alignment evidence | 09:39:56 04 Mar 2015 | 10:32:47 04 Mar 2015 | 52 minutes 51 seconds |
| Polymorphism statistics | 10:32:47 04 Mar 2015 | 10:32:51 04 Mar 2015 | 4 seconds |
| Output | 10:32:51 04 Mar 2015 | 10:36:27 04 Mar 2015 | 3 minutes 36 seconds |
| Total | 1 hour 31 minutes 58 seconds | ||
