mutation predictions | marginal predictions | summary statistics | genome diff | command line log
|
breseq version 0.35.4 revision f352f80f4bc9
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
| read file | reads | bases | passed filters | average | longest | mapped | |
|---|---|---|---|---|---|---|---|
| errors | TF_KALE_crp_A1_F86_I0_R1_S59_L001_R1_001.good.fq | 340,009 | 43,883,695 | 100.0% | 129.1 bases | 137 bases | 97.7% |
| errors | TF_KALE_crp_A1_F86_I0_R1_S59_L001_R2_001.good.fq | 340,009 | 43,884,625 | 100.0% | 129.1 bases | 137 bases | 95.8% |
| errors | TF_KALE_crp_A1_F86_I0_R1_S59_L002_R1_001.good.fq | 340,222 | 43,894,923 | 100.0% | 129.0 bases | 137 bases | 98.4% |
| errors | TF_KALE_crp_A1_F86_I0_R1_S59_L002_R2_001.good.fq | 340,222 | 43,896,003 | 100.0% | 129.0 bases | 137 bases | 97.0% |
| errors | TF_KALE_crp_A1_F86_I0_R1_S59_L003_R1_001.good.fq | 339,993 | 43,823,777 | 100.0% | 128.9 bases | 137 bases | 98.3% |
| errors | TF_KALE_crp_A1_F86_I0_R1_S59_L003_R2_001.good.fq | 339,993 | 43,824,352 | 100.0% | 128.9 bases | 137 bases | 97.2% |
| errors | TF_KALE_crp_A1_F86_I0_R1_S59_L004_R1_001.good.fq | 347,994 | 44,798,656 | 100.0% | 128.7 bases | 137 bases | 98.6% |
| errors | TF_KALE_crp_A1_F86_I0_R1_S59_L004_R2_001.good.fq | 347,994 | 44,800,933 | 100.0% | 128.7 bases | 137 bases | 97.7% |
| total | 2,736,436 | 352,806,964 | 100.0% | 128.9 bases | 137 bases | 97.6% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_000913 | 4,641,652 | 73.5 | 4.4 | 100.0% | 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 | 1715 |
| 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 | 84 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.005 |
| reference sequence | pr(no read start) |
|---|---|
| NC_000913 | 0.83446 |
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 |
| Minimum probablilty assigned that no mapped read will start at a given position and strand for junction prediction | 0.1 |
| Junction allow suboptimal matches | FALSE |
| 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 | 2.2.6 |
| R | 3.4.4 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 21:20:56 22 Apr 2021 | 21:21:43 22 Apr 2021 | 47 seconds |
| Read alignment to reference genome | 21:21:43 22 Apr 2021 | 21:27:19 22 Apr 2021 | 5 minutes 36 seconds |
| Preprocessing alignments for candidate junction identification | 21:27:19 22 Apr 2021 | 21:27:51 22 Apr 2021 | 32 seconds |
| Preliminary analysis of coverage distribution | 21:27:51 22 Apr 2021 | 21:29:25 22 Apr 2021 | 1 minute 34 seconds |
| Identifying junction candidates | 21:29:25 22 Apr 2021 | 21:29:25 22 Apr 2021 | 0 seconds |
| Re-alignment to junction candidates | 21:29:25 22 Apr 2021 | 21:30:46 22 Apr 2021 | 1 minute 21 seconds |
| Resolving best read alignments | 21:30:46 22 Apr 2021 | 21:31:32 22 Apr 2021 | 46 seconds |
| Creating BAM files | 21:31:32 22 Apr 2021 | 21:32:57 22 Apr 2021 | 1 minute 25 seconds |
| Tabulating error counts | 21:32:57 22 Apr 2021 | 21:33:29 22 Apr 2021 | 32 seconds |
| Re-calibrating base error rates | 21:33:29 22 Apr 2021 | 21:33:32 22 Apr 2021 | 3 seconds |
| Examining read alignment evidence | 21:33:32 22 Apr 2021 | 21:55:45 22 Apr 2021 | 22 minutes 13 seconds |
| Polymorphism statistics | 21:55:45 22 Apr 2021 | 21:55:46 22 Apr 2021 | 1 second |
| Output | 21:55:46 22 Apr 2021 | 21:55:59 22 Apr 2021 | 13 seconds |
| Total | 35 minutes 3 seconds | ||
