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 | SvNSRound4_2_112_S2322_L007_R1_001.good.fq | 958,810 | 132,743,450 | 100.0% | 138.4 bases | 151 bases | 93.5% |
errors | SvNSRound4_2_112_S2322_L007_R2_001.good.fq | 958,810 | 132,743,450 | 100.0% | 138.4 bases | 151 bases | 92.8% |
errors | SvNSRound4_2_112_S2322_L008_R1_001.good.fq | 598,814 | 82,618,022 | 100.0% | 138.0 bases | 150 bases | 93.3% |
errors | SvNSRound4_2_112_S2322_L008_R2_001.good.fq | 598,814 | 82,618,022 | 100.0% | 138.0 bases | 150 bases | 92.0% |
total | 3,115,248 | 430,722,944 | 100.0% | 138.3 bases | 151 bases | 92.9% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_000913_3_bme_pgi | 4,641,653 | 80.9 | 2.1 | 100.0% | Escherichia coli str. K-12 substr. MG1655, B. melitensis pgi gene, complete genome. |
total | 4,641,653 | 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 | 100020 |
Coverage evenness (position-hash) score of junction candidates | ≥ 2 | ≥ 3 |
Test this many junction candidates (n). May be smaller if not enough passed the coverage evenness threshold | 100 ≤ n ≤ 5000 | 843 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.057 |
reference sequence | pr(no read start) |
---|---|
NC_000913_3_bme_pgi | 0.75800 |
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 | 0.75 |
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 | 2.2.6 |
R | 3.4.4 |
step | start | end | elapsed |
---|---|---|---|
Read and reference sequence file input | 18:23:44 19 Dec 2020 | 18:26:32 19 Dec 2020 | 2 minutes 48 seconds |
Read alignment to reference genome | 18:26:33 19 Dec 2020 | 18:51:12 19 Dec 2020 | 24 minutes 39 seconds |
Preprocessing alignments for candidate junction identification | 18:51:12 19 Dec 2020 | 18:53:36 19 Dec 2020 | 2 minutes 24 seconds |
Preliminary analysis of coverage distribution | 18:53:36 19 Dec 2020 | 18:58:42 19 Dec 2020 | 5 minutes 6 seconds |
Identifying junction candidates | 18:58:42 19 Dec 2020 | 20:23:10 19 Dec 2020 | 1 hour 24 minutes 28 seconds |
Re-alignment to junction candidates | 20:23:10 19 Dec 2020 | 20:33:20 19 Dec 2020 | 10 minutes 10 seconds |
Resolving best read alignments | 20:33:20 19 Dec 2020 | 20:36:53 19 Dec 2020 | 3 minutes 33 seconds |
Creating BAM files | 20:36:53 19 Dec 2020 | 20:41:35 19 Dec 2020 | 4 minutes 42 seconds |
Tabulating error counts | 20:41:35 19 Dec 2020 | 20:43:29 19 Dec 2020 | 1 minute 54 seconds |
Re-calibrating base error rates | 20:43:29 19 Dec 2020 | 20:43:34 19 Dec 2020 | 5 seconds |
Examining read alignment evidence | 20:43:34 19 Dec 2020 | 21:07:50 19 Dec 2020 | 24 minutes 16 seconds |
Polymorphism statistics | 21:07:50 19 Dec 2020 | 21:07:54 19 Dec 2020 | 4 seconds |
Output | 21:07:54 19 Dec 2020 | 21:09:08 19 Dec 2020 | 1 minute 14 seconds |
Total | 2 hours 45 minutes 23 seconds |