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_10_35_S2356_L007_R1_001.good.fq | 1,788,988 | 230,349,370 | 100.0% | 128.8 bases | 150 bases | 94.9% |
errors | SvNSRound4_10_35_S2356_L007_R2_001.good.fq | 1,788,988 | 230,349,370 | 100.0% | 128.8 bases | 150 bases | 94.0% |
errors | SvNSRound4_10_35_S2356_L008_R1_001.good.fq | 1,104,508 | 143,252,018 | 100.0% | 129.7 bases | 150 bases | 94.4% |
errors | SvNSRound4_10_35_S2356_L008_R2_001.good.fq | 1,104,508 | 143,252,018 | 100.0% | 129.7 bases | 150 bases | 93.2% |
total | 5,786,992 | 747,202,776 | 100.0% | 129.1 bases | 150 bases | 94.2% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_000913_3_bme_pgi | 4,641,653 | 150.5 | 2.3 | 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 | 100002 |
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 | 623 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.041 |
reference sequence | pr(no read start) |
---|---|
NC_000913_3_bme_pgi | 0.59684 |
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 | 18:42:34 19 Dec 2020 | 18:47:18 19 Dec 2020 | 4 minutes 44 seconds |
Read alignment to reference genome | 18:47:19 19 Dec 2020 | 19:26:51 19 Dec 2020 | 39 minutes 32 seconds |
Preprocessing alignments for candidate junction identification | 19:26:51 19 Dec 2020 | 19:31:30 19 Dec 2020 | 4 minutes 39 seconds |
Preliminary analysis of coverage distribution | 19:31:30 19 Dec 2020 | 19:40:23 19 Dec 2020 | 8 minutes 53 seconds |
Identifying junction candidates | 19:40:23 19 Dec 2020 | 19:57:08 19 Dec 2020 | 16 minutes 45 seconds |
Re-alignment to junction candidates | 19:57:08 19 Dec 2020 | 20:08:05 19 Dec 2020 | 10 minutes 57 seconds |
Resolving best read alignments | 20:08:05 19 Dec 2020 | 20:13:28 19 Dec 2020 | 5 minutes 23 seconds |
Creating BAM files | 20:13:28 19 Dec 2020 | 20:21:47 19 Dec 2020 | 8 minutes 19 seconds |
Tabulating error counts | 20:21:47 19 Dec 2020 | 20:24:59 19 Dec 2020 | 3 minutes 12 seconds |
Re-calibrating base error rates | 20:24:59 19 Dec 2020 | 20:25:03 19 Dec 2020 | 4 seconds |
Examining read alignment evidence | 20:25:03 19 Dec 2020 | 21:04:26 19 Dec 2020 | 39 minutes 23 seconds |
Polymorphism statistics | 21:04:26 19 Dec 2020 | 21:04:30 19 Dec 2020 | 4 seconds |
Output | 21:04:30 19 Dec 2020 | 21:05:40 19 Dec 2020 | 1 minute 10 seconds |
Total | 2 hours 23 minutes 5 seconds |