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-4_S26_L001_R1_001.good.fq | 184,417 | 26,976,470 | 100.0% | 146.3 bases | 148 bases | 97.8% |
| errors | Ferulic-4_S26_L001_R2_001.good.fq | 184,417 | 26,962,387 | 100.0% | 146.2 bases | 148 bases | 97.1% |
| errors | Ferulic-4_S26_L002_R1_001.good.fq | 168,550 | 24,648,337 | 100.0% | 146.2 bases | 148 bases | 97.9% |
| errors | Ferulic-4_S26_L002_R2_001.good.fq | 168,550 | 24,636,114 | 100.0% | 146.2 bases | 148 bases | 96.8% |
| errors | Ferulic-4_S26_L003_R1_001.good.fq | 169,542 | 24,798,805 | 100.0% | 146.3 bases | 148 bases | 97.8% |
| errors | Ferulic-4_S26_L003_R2_001.good.fq | 169,542 | 24,785,969 | 100.0% | 146.2 bases | 148 bases | 97.1% |
| errors | Ferulic-4_S26_L004_R1_001.good.fq | 160,484 | 23,468,333 | 100.0% | 146.2 bases | 148 bases | 97.9% |
| errors | Ferulic-4_S26_L004_R2_001.good.fq | 160,484 | 23,457,768 | 100.0% | 146.2 bases | 148 bases | 96.6% |
| total | 1,365,986 | 199,734,183 | 100.0% | 146.2 bases | 148 bases | 97.4% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_002947 | 6,181,873 | 29.7 | 1.7 | 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 | 15731 |
| 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 | 729 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.036 |
| reference sequence | pr(no read start) |
|---|---|
| NC_002947 | 0.91042 |
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 | 22:29:09 17 Feb 2020 | 22:29:30 17 Feb 2020 | 21 seconds |
| Read alignment to reference genome | 22:29:31 17 Feb 2020 | 22:32:29 17 Feb 2020 | 2 minutes 58 seconds |
| Preprocessing alignments for candidate junction identification | 22:32:29 17 Feb 2020 | 22:32:49 17 Feb 2020 | 20 seconds |
| Preliminary analysis of coverage distribution | 22:32:49 17 Feb 2020 | 22:33:36 17 Feb 2020 | 47 seconds |
| Identifying junction candidates | 22:33:36 17 Feb 2020 | 22:33:48 17 Feb 2020 | 12 seconds |
| Re-alignment to junction candidates | 22:33:48 17 Feb 2020 | 22:35:02 17 Feb 2020 | 1 minute 14 seconds |
| Resolving best read alignments | 22:35:02 17 Feb 2020 | 22:35:33 17 Feb 2020 | 31 seconds |
| Creating BAM files | 22:35:33 17 Feb 2020 | 22:36:15 17 Feb 2020 | 42 seconds |
| Tabulating error counts | 22:36:15 17 Feb 2020 | 22:36:30 17 Feb 2020 | 15 seconds |
| Re-calibrating base error rates | 22:36:30 17 Feb 2020 | 22:36:33 17 Feb 2020 | 3 seconds |
| Examining read alignment evidence | 22:36:33 17 Feb 2020 | 22:39:50 17 Feb 2020 | 3 minutes 17 seconds |
| Polymorphism statistics | 22:39:50 17 Feb 2020 | 22:39:50 17 Feb 2020 | 0 seconds |
| Output | 22:39:50 17 Feb 2020 | 22:40:20 17 Feb 2020 | 30 seconds |
| Total | 11 minutes 10 seconds | ||
