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breseq version 0.26.0
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
read file | reads | bases | passed filters | average | longest | mapped | |
---|---|---|---|---|---|---|---|
errors | 2Xyl_S4_L001_R2_001 | 1,251,945 | 361,221,127 | 100.0% | 288.5 bases | 301 bases | 80.1% |
errors | 2Xyl_S4_L001_R1_001 | 1,251,985 | 357,974,071 | 100.0% | 285.9 bases | 301 bases | 96.9% |
total | 2,503,930 | 719,195,198 | 100.0% | 287.2 bases | 301 bases | 88.5% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_000913 | 4,641,652 | 141.2 | 3.9 | 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 | 3691 |
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 | 165 |
Total length of all junction candidates (factor times the reference genome length) | ≥ 0.1 | 0.022 |
reference sequence | pr(no read start) |
---|---|
NC_000913 | 0.87270 |
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 |
Polymorphism E-value cutoff | 2 |
Polymorphism frequency cutoff | 0.05 |
Polymorphism minimum coverage each strand | 2 |
Polymorphism bias cutoff | 0.001 |
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 | ≥2 bases |
step | start | end | elapsed |
---|---|---|---|
Read and reference sequence file input | 03:07:44 17 Apr 2015 | 03:08:45 17 Apr 2015 | 1 minute 1 second |
Read alignment to reference genome | 03:08:45 17 Apr 2015 | 03:16:02 17 Apr 2015 | 7 minutes 17 seconds |
Preprocessing alignments for candidate junction identification | 03:16:02 17 Apr 2015 | 03:17:17 17 Apr 2015 | 1 minute 15 seconds |
Preliminary analysis of coverage distribution | 03:17:17 17 Apr 2015 | 03:20:56 17 Apr 2015 | 3 minutes 39 seconds |
Identifying junction candidates | 03:20:56 17 Apr 2015 | 03:20:57 17 Apr 2015 | 1 second |
Re-alignment to junction candidates | 03:20:57 17 Apr 2015 | 03:21:34 17 Apr 2015 | 37 seconds |
Resolving alignments with junction candidates | 03:21:34 17 Apr 2015 | 03:23:28 17 Apr 2015 | 1 minute 54 seconds |
Creating BAM files | 03:23:28 17 Apr 2015 | 03:25:43 17 Apr 2015 | 2 minutes 15 seconds |
Tabulating error counts | 03:25:43 17 Apr 2015 | 03:29:12 17 Apr 2015 | 3 minutes 29 seconds |
Re-calibrating base error rates | 03:29:12 17 Apr 2015 | 03:29:13 17 Apr 2015 | 1 second |
Examining read alignment evidence | 03:29:13 17 Apr 2015 | 06:21:07 17 Apr 2015 | 2 hours 51 minutes 54 seconds |
Polymorphism statistics | 06:21:07 17 Apr 2015 | 06:21:08 17 Apr 2015 | 1 second |
Output | 06:21:08 17 Apr 2015 | 06:21:56 17 Apr 2015 | 48 seconds |
Total | 3 hours 14 minutes 12 seconds |