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breseq version 0.38.1
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
| read file | reads | bases | passed filters | average | longest | mapped | |
|---|---|---|---|---|---|---|---|
| errors | 11109049673_S2060_Dung_Dnfi_c10.rawdata‡ | 963,957 | 192,791,400 | 98.3% | 200.0 bases | 200 bases | 94.3% |
| total | 963,957 | 192,791,400 | 98.3% | 200.0 bases | 200 bases | 94.3% |
‡ Read and base numbers are after long reads in this file were split to exactly 200 bases (extra bases discarded)
| seq id | length | fit mean | fit relative_variance | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | NC_010473 | 4,686,137 | 37.4 | 1.3 | 100.0% | Escherichia coli str. K-12 substr. DH10B, complete sequence. |
| total | 4,686,137 | 100.0% |
fit relative_variance 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 | 100039 |
| 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 | 864 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.074 |
| reference sequence | pr(no read start) |
|---|---|
| NC_010473 | 0.91267 |
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 | ≤ 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 | 0.8 |
| 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 | NO |
| Skip indel polymorphisms in homopolymers runs of | ≥4 bases |
| Skip base substitutions when they create a homopolymer flanked on each side by | OFF |
| program | version |
|---|---|
| bowtie2 | 2.4.4 |
| R | 4.1.1 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 10:34:32 29 Sep 2024 | 10:34:52 29 Sep 2024 | 20 seconds |
| Read alignment to reference genome | 10:34:52 29 Sep 2024 | 10:35:49 29 Sep 2024 | 57 seconds |
| Preprocessing alignments for candidate junction identification | 10:35:49 29 Sep 2024 | 10:36:10 29 Sep 2024 | 21 seconds |
| Preliminary analysis of coverage distribution | 10:36:10 29 Sep 2024 | 10:36:45 29 Sep 2024 | 35 seconds |
| Identifying junction candidates | 10:36:45 29 Sep 2024 | 10:37:06 29 Sep 2024 | 21 seconds |
| Re-alignment to junction candidates | 10:37:06 29 Sep 2024 | 10:37:21 29 Sep 2024 | 15 seconds |
| Resolving best read alignments | 10:37:21 29 Sep 2024 | 10:37:52 29 Sep 2024 | 31 seconds |
| Creating BAM files | 10:37:52 29 Sep 2024 | 10:38:19 29 Sep 2024 | 27 seconds |
| Tabulating error counts | 10:38:19 29 Sep 2024 | 10:38:48 29 Sep 2024 | 29 seconds |
| Re-calibrating base error rates | 10:38:48 29 Sep 2024 | 10:38:49 29 Sep 2024 | 1 second |
| Examining read alignment evidence | 10:38:49 29 Sep 2024 | 10:42:46 29 Sep 2024 | 3 minutes 57 seconds |
| Polymorphism statistics | 10:42:46 29 Sep 2024 | 10:42:47 29 Sep 2024 | 1 second |
| Output | 10:42:47 29 Sep 2024 | 10:42:58 29 Sep 2024 | 11 seconds |
| Output :: Mutation Prediction | 10:42:47 29 Sep 2024 | 10:42:51 29 Sep 2024 | 4 seconds |
| Output :: Mutation Annotation | 10:42:51 29 Sep 2024 | 10:42:51 29 Sep 2024 | 0 seconds |
| Total | 8 minutes 30 seconds | ||