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-IND_KHP_HOT_A11_F142_I1_R1_S47_L004_R1_001 | 1,574,057 | 157,357,177 | 100.0% | 100.0 bases | 100 bases | 96.5% |
| errors | qtrim-IND_KHP_HOT_A11_F142_I1_R1_S47_L004_R2_001 | 1,574,047 | 157,109,664 | 100.0% | 99.8 bases | 100 bases | 96.1% |
| total | 3,148,104 | 314,466,841 | 100.0% | 99.9 bases | 100 bases | 96.3% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 64.8 | 1.6 | 98.1% | 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 | 57846 |
| Coverage evenness (position-hash) score of junction candidates | ≥ 2 | ≥ 3 |
| Test this many junction candidates (n). May be smaller if not enough passed the coverage evenness threshold | 100 ≤ n ≤ 5000 | 548 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.024 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.74487 |
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 | 13:21:53 04 Jan 2017 | 13:22:26 04 Jan 2017 | 33 seconds |
| Read alignment to reference genome | 13:22:27 04 Jan 2017 | 13:24:16 04 Jan 2017 | 1 minute 49 seconds |
| Preprocessing alignments for candidate junction identification | 13:24:16 04 Jan 2017 | 13:25:23 04 Jan 2017 | 1 minute 7 seconds |
| Preliminary analysis of coverage distribution | 13:25:23 04 Jan 2017 | 13:26:37 04 Jan 2017 | 1 minute 14 seconds |
| Identifying junction candidates | 13:26:37 04 Jan 2017 | 13:28:31 04 Jan 2017 | 1 minute 54 seconds |
| Re-alignment to junction candidates | 13:28:31 04 Jan 2017 | 13:28:53 04 Jan 2017 | 22 seconds |
| Resolving alignments with junction candidates | 13:28:53 04 Jan 2017 | 13:30:44 04 Jan 2017 | 1 minute 51 seconds |
| Creating BAM files | 13:30:44 04 Jan 2017 | 13:31:28 04 Jan 2017 | 44 seconds |
| Tabulating error counts | 13:31:28 04 Jan 2017 | 13:32:50 04 Jan 2017 | 1 minute 22 seconds |
| Re-calibrating base error rates | 13:32:50 04 Jan 2017 | 13:32:50 04 Jan 2017 | 0 seconds |
| Examining read alignment evidence | 13:32:50 04 Jan 2017 | 13:43:13 04 Jan 2017 | 10 minutes 23 seconds |
| Polymorphism statistics | 13:43:13 04 Jan 2017 | 13:43:14 04 Jan 2017 | 1 second |
| Output | 13:43:14 04 Jan 2017 | 13:43:52 04 Jan 2017 | 38 seconds |
| Total | 21 minutes 58 seconds | ||
