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breseq version 0.33.1 revision 8505477f25b3
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
| read file | reads | bases | passed filters | average | longest | mapped | |
|---|---|---|---|---|---|---|---|
| errors | ALE-18_S18_L001_R1_001.good.fq | 381,173 | 53,246,667 | 100.0% | 139.7 bases | 149 bases | 93.6% |
| errors | ALE-18_S18_L001_R2_001.good.fq | 381,173 | 52,978,159 | 100.0% | 139.0 bases | 149 bases | 94.3% |
| errors | ALE-18_S18_L002_R1_001.good.fq | 377,650 | 52,643,650 | 100.0% | 139.4 bases | 149 bases | 94.7% |
| errors | ALE-18_S18_L002_R2_001.good.fq | 377,650 | 52,444,908 | 100.0% | 138.9 bases | 149 bases | 94.8% |
| errors | ALE-18_S18_L003_R1_001.good.fq | 391,714 | 54,573,401 | 100.0% | 139.3 bases | 149 bases | 94.6% |
| errors | ALE-18_S18_L003_R2_001.good.fq | 391,714 | 54,330,044 | 100.0% | 138.7 bases | 149 bases | 95.2% |
| errors | ALE-18_S18_L004_R1_001.good.fq | 363,598 | 50,647,614 | 100.0% | 139.3 bases | 149 bases | 94.5% |
| errors | ALE-18_S18_L004_R2_001.good.fq | 363,598 | 50,466,225 | 100.0% | 138.8 bases | 149 bases | 94.4% |
| total | 3,028,270 | 421,330,668 | 100.0% | 139.1 bases | 149 bases | 94.5% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_002947 | 6,181,873 | 64.6 | 2.3 | 100.0% | Pseudomonas putida KT2440 chromosome, complete genome. |
| total | 6,181,873 | 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 | 66162 |
| 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 | 927 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.046 |
| reference sequence | pr(no read start) |
|---|---|
| NC_002947 | 0.80881 |
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 |
| Consensus frequency cutoff | 0.75 |
| Consensus minimum variant coverage each strand | OFF |
| Consensus minimum total coverage each strand | OFF |
| Consensus minimum variant coverage | OFF |
| Consensus minimum total coverage | OFF |
| Polymorphism E-value cutoff | 2 |
| Polymorphism frequency cutoff | 0.05 |
| Polymorphism minimum variant coverage each strand | 2 |
| Polymorphism minimum total coverage each strand | OFF |
| Polymorphism minimum variant coverage | OFF |
| Polymorphism minimum total coverage | OFF |
| Polymorphism bias cutoff | OFF |
| 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 | ≥5 bases |
| program | version |
|---|---|
| bowtie2 | 2.3.4.1 |
| R | 3.4.4 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 23:39:20 18 Feb 2020 | 23:40:05 18 Feb 2020 | 45 seconds |
| Read alignment to reference genome | 23:40:05 18 Feb 2020 | 23:46:35 18 Feb 2020 | 6 minutes 30 seconds |
| Preprocessing alignments for candidate junction identification | 23:46:35 18 Feb 2020 | 23:47:17 18 Feb 2020 | 42 seconds |
| Preliminary analysis of coverage distribution | 23:47:17 18 Feb 2020 | 23:48:57 18 Feb 2020 | 1 minute 40 seconds |
| Identifying junction candidates | 23:48:57 18 Feb 2020 | 00:00:08 19 Feb 2020 | 11 minutes 11 seconds |
| Re-alignment to junction candidates | 00:00:08 19 Feb 2020 | 00:02:27 19 Feb 2020 | 2 minutes 19 seconds |
| Resolving best read alignments | 00:02:27 19 Feb 2020 | 00:03:32 19 Feb 2020 | 1 minute 5 seconds |
| Creating BAM files | 00:03:32 19 Feb 2020 | 00:05:05 19 Feb 2020 | 1 minute 33 seconds |
| Tabulating error counts | 00:05:05 19 Feb 2020 | 00:05:36 19 Feb 2020 | 31 seconds |
| Re-calibrating base error rates | 00:05:36 19 Feb 2020 | 00:05:38 19 Feb 2020 | 2 seconds |
| Examining read alignment evidence | 00:05:38 19 Feb 2020 | 00:21:41 19 Feb 2020 | 16 minutes 3 seconds |
| Polymorphism statistics | 00:21:41 19 Feb 2020 | 00:21:43 19 Feb 2020 | 2 seconds |
| Output | 00:21:43 19 Feb 2020 | 00:27:23 19 Feb 2020 | 5 minutes 40 seconds |
| Total | 48 minutes 3 seconds | ||