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_A10_F044_I1_R1_S43_L004_R2_001 | 1,600,763 | 159,672,586 | 100.0% | 99.7 bases | 100 bases | 95.8% |
| errors | qtrim-IND_KHP_HOT_A10_F044_I1_R1_S43_L004_R1_001 | 1,600,778 | 160,026,841 | 100.0% | 100.0 bases | 100 bases | 96.5% |
| total | 3,201,541 | 319,699,427 | 100.0% | 99.9 bases | 100 bases | 96.2% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 65.8 | 1.5 | 98.0% | 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 | 73388 |
| 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 | 757 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.034 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.74192 |
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 | 09:42:44 15 Jan 2017 | 09:43:18 15 Jan 2017 | 34 seconds |
| Read alignment to reference genome | 09:43:18 15 Jan 2017 | 09:44:49 15 Jan 2017 | 1 minute 31 seconds |
| Preprocessing alignments for candidate junction identification | 09:44:49 15 Jan 2017 | 09:46:08 15 Jan 2017 | 1 minute 19 seconds |
| Preliminary analysis of coverage distribution | 09:46:08 15 Jan 2017 | 09:47:30 15 Jan 2017 | 1 minute 22 seconds |
| Identifying junction candidates | 09:47:30 15 Jan 2017 | 09:52:19 15 Jan 2017 | 4 minutes 49 seconds |
| Re-alignment to junction candidates | 09:52:19 15 Jan 2017 | 09:52:41 15 Jan 2017 | 22 seconds |
| Resolving alignments with junction candidates | 09:52:41 15 Jan 2017 | 09:54:46 15 Jan 2017 | 2 minutes 5 seconds |
| Creating BAM files | 09:54:46 15 Jan 2017 | 09:55:32 15 Jan 2017 | 46 seconds |
| Tabulating error counts | 09:55:32 15 Jan 2017 | 09:56:59 15 Jan 2017 | 1 minute 27 seconds |
| Re-calibrating base error rates | 09:56:59 15 Jan 2017 | 09:56:59 15 Jan 2017 | 0 seconds |
| Examining read alignment evidence | 09:56:59 15 Jan 2017 | 10:08:03 15 Jan 2017 | 11 minutes 4 seconds |
| Polymorphism statistics | 10:08:03 15 Jan 2017 | 10:08:04 15 Jan 2017 | 1 second |
| Output | 10:08:04 15 Jan 2017 | 10:08:37 15 Jan 2017 | 33 seconds |
| Total | 25 minutes 53 seconds | ||
