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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-13_S13_L001_R1_001.good.fq | 331,019 | 46,819,834 | 100.0% | 141.4 bases | 149 bases | 93.9% |
| errors | ALE-13_S13_L001_R2_001.good.fq | 331,019 | 46,626,376 | 100.0% | 140.9 bases | 149 bases | 94.6% |
| errors | ALE-13_S13_L002_R1_001.good.fq | 322,573 | 45,532,762 | 100.0% | 141.2 bases | 149 bases | 95.2% |
| errors | ALE-13_S13_L002_R2_001.good.fq | 322,573 | 45,385,475 | 100.0% | 140.7 bases | 149 bases | 95.1% |
| errors | ALE-13_S13_L003_R1_001.good.fq | 337,213 | 47,561,782 | 100.0% | 141.0 bases | 149 bases | 95.1% |
| errors | ALE-13_S13_L003_R2_001.good.fq | 337,213 | 47,386,467 | 100.0% | 140.5 bases | 149 bases | 95.6% |
| errors | ALE-13_S13_L004_R1_001.good.fq | 308,851 | 43,554,966 | 100.0% | 141.0 bases | 149 bases | 95.0% |
| errors | ALE-13_S13_L004_R2_001.good.fq | 308,851 | 43,414,919 | 100.0% | 140.6 bases | 149 bases | 94.7% |
| total | 2,599,312 | 366,282,581 | 100.0% | 140.9 bases | 149 bases | 94.9% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_002947 | 6,181,873 | 54.2 | 2.2 | 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 | 51714 |
| 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 | 437 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.022 |
| reference sequence | pr(no read start) |
|---|---|
| NC_002947 | 0.83412 |
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 | 01:11:36 18 Feb 2020 | 01:12:15 18 Feb 2020 | 39 seconds |
| Read alignment to reference genome | 01:12:15 18 Feb 2020 | 01:17:53 18 Feb 2020 | 5 minutes 38 seconds |
| Preprocessing alignments for candidate junction identification | 01:17:53 18 Feb 2020 | 01:18:30 18 Feb 2020 | 37 seconds |
| Preliminary analysis of coverage distribution | 01:18:30 18 Feb 2020 | 01:19:58 18 Feb 2020 | 1 minute 28 seconds |
| Identifying junction candidates | 01:19:58 18 Feb 2020 | 01:25:53 18 Feb 2020 | 5 minutes 55 seconds |
| Re-alignment to junction candidates | 01:25:53 18 Feb 2020 | 01:27:38 18 Feb 2020 | 1 minute 45 seconds |
| Resolving best read alignments | 01:27:38 18 Feb 2020 | 01:28:35 18 Feb 2020 | 57 seconds |
| Creating BAM files | 01:28:35 18 Feb 2020 | 01:29:57 18 Feb 2020 | 1 minute 22 seconds |
| Tabulating error counts | 01:29:57 18 Feb 2020 | 01:30:23 18 Feb 2020 | 26 seconds |
| Re-calibrating base error rates | 01:30:23 18 Feb 2020 | 01:30:26 18 Feb 2020 | 3 seconds |
| Examining read alignment evidence | 01:30:26 18 Feb 2020 | 01:44:15 18 Feb 2020 | 13 minutes 49 seconds |
| Polymorphism statistics | 01:44:15 18 Feb 2020 | 01:44:17 18 Feb 2020 | 2 seconds |
| Output | 01:44:17 18 Feb 2020 | 01:47:43 18 Feb 2020 | 3 minutes 26 seconds |
| Total | 36 minutes 7 seconds | ||