mutation predictions | marginal predictions | summary statistics | genome diff | command line log
|
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 | Ferulic-1_S23_L001_R1_001.good.fq | 186,010 | 27,206,932 | 100.0% | 146.3 bases | 148 bases | 97.1% |
| errors | Ferulic-1_S23_L001_R2_001.good.fq | 186,010 | 27,192,890 | 100.0% | 146.2 bases | 148 bases | 96.2% |
| errors | Ferulic-1_S23_L002_R1_001.good.fq | 171,694 | 25,114,103 | 100.0% | 146.3 bases | 148 bases | 97.1% |
| errors | Ferulic-1_S23_L002_R2_001.good.fq | 171,694 | 25,100,989 | 100.0% | 146.2 bases | 148 bases | 96.0% |
| errors | Ferulic-1_S23_L003_R1_001.good.fq | 172,356 | 25,211,279 | 100.0% | 146.3 bases | 148 bases | 97.0% |
| errors | Ferulic-1_S23_L003_R2_001.good.fq | 172,356 | 25,194,952 | 100.0% | 146.2 bases | 148 bases | 96.2% |
| errors | Ferulic-1_S23_L004_R1_001.good.fq | 162,651 | 23,783,300 | 100.0% | 146.2 bases | 148 bases | 97.0% |
| errors | Ferulic-1_S23_L004_R2_001.good.fq | 162,651 | 23,770,339 | 100.0% | 146.1 bases | 148 bases | 95.8% |
| total | 1,385,422 | 202,574,784 | 100.0% | 146.2 bases | 148 bases | 96.5% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_002947 | 6,181,873 | 31.5 | 1.8 | 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 | 18796 |
| 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 | 1038 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.051 |
| reference sequence | pr(no read start) |
|---|---|
| NC_002947 | 0.90646 |
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 | 0.75 |
| 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 | 10 |
| Polymorphism frequency cutoff | 0.2 |
| Polymorphism minimum variant coverage each strand | OFF |
| 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 | OFF |
| Skip base substitutions when they create a homopolymer flanked on each side by | OFF |
| program | version |
|---|---|
| bowtie2 | 2.3.4.1 |
| R | 3.4.4 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 06:13:14 19 Feb 2020 | 06:13:36 19 Feb 2020 | 22 seconds |
| Read alignment to reference genome | 06:13:37 19 Feb 2020 | 06:16:37 19 Feb 2020 | 3 minutes 0 seconds |
| Preprocessing alignments for candidate junction identification | 06:16:37 19 Feb 2020 | 06:16:57 19 Feb 2020 | 20 seconds |
| Preliminary analysis of coverage distribution | 06:16:57 19 Feb 2020 | 06:17:43 19 Feb 2020 | 46 seconds |
| Identifying junction candidates | 06:17:43 19 Feb 2020 | 06:17:56 19 Feb 2020 | 13 seconds |
| Re-alignment to junction candidates | 06:17:56 19 Feb 2020 | 06:19:00 19 Feb 2020 | 1 minute 4 seconds |
| Resolving best read alignments | 06:19:00 19 Feb 2020 | 06:19:31 19 Feb 2020 | 31 seconds |
| Creating BAM files | 06:19:31 19 Feb 2020 | 06:20:13 19 Feb 2020 | 42 seconds |
| Tabulating error counts | 06:20:13 19 Feb 2020 | 06:20:28 19 Feb 2020 | 15 seconds |
| Re-calibrating base error rates | 06:20:28 19 Feb 2020 | 06:20:30 19 Feb 2020 | 2 seconds |
| Examining read alignment evidence | 06:20:30 19 Feb 2020 | 06:23:40 19 Feb 2020 | 3 minutes 10 seconds |
| Polymorphism statistics | 06:23:40 19 Feb 2020 | 06:23:40 19 Feb 2020 | 0 seconds |
| Output | 06:23:40 19 Feb 2020 | 06:24:04 19 Feb 2020 | 24 seconds |
| Total | 10 minutes 49 seconds | ||
