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_8_99_S2349_L007_R1_001.good.fq | 1,180,684 | 160,101,152 | 100.0% | 135.6 bases | 150 bases | 96.5% |
errors | SvNSRound4_8_99_S2349_L007_R2_001.good.fq | 1,180,684 | 160,101,152 | 100.0% | 135.6 bases | 150 bases | 95.5% |
errors | SvNSRound4_8_99_S2349_L008_R1_001.good.fq | 741,442 | 101,161,177 | 100.0% | 136.4 bases | 150 bases | 96.2% |
errors | SvNSRound4_8_99_S2349_L008_R2_001.good.fq | 741,442 | 101,161,177 | 100.0% | 136.4 bases | 150 bases | 94.8% |
total | 3,844,252 | 522,524,658 | 100.0% | 135.9 bases | 150 bases | 95.8% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_000913_3_hsa_tpiA | 4,641,634 | 107.4 | 2.0 | 100.0% | Escherichia coli str. K-12 substr. MG1655, H. sapien tpiA gene, complete genome. |
total | 4,641,634 | 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 | 86598 |
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 | 974 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.065 |
reference sequence | pr(no read start) |
---|---|
NC_000913_3_hsa_tpiA | 0.70003 |
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 | 18:29:16 19 Dec 2020 | 18:32:29 19 Dec 2020 | 3 minutes 13 seconds |
Read alignment to reference genome | 18:32:30 19 Dec 2020 | 19:00:04 19 Dec 2020 | 27 minutes 34 seconds |
Preprocessing alignments for candidate junction identification | 19:00:04 19 Dec 2020 | 19:03:14 19 Dec 2020 | 3 minutes 10 seconds |
Preliminary analysis of coverage distribution | 19:03:14 19 Dec 2020 | 19:09:40 19 Dec 2020 | 6 minutes 26 seconds |
Identifying junction candidates | 19:09:40 19 Dec 2020 | 19:35:47 19 Dec 2020 | 26 minutes 7 seconds |
Re-alignment to junction candidates | 19:35:47 19 Dec 2020 | 19:44:26 19 Dec 2020 | 8 minutes 39 seconds |
Resolving best read alignments | 19:44:26 19 Dec 2020 | 19:48:08 19 Dec 2020 | 3 minutes 42 seconds |
Creating BAM files | 19:48:08 19 Dec 2020 | 19:53:51 19 Dec 2020 | 5 minutes 43 seconds |
Tabulating error counts | 19:53:51 19 Dec 2020 | 19:56:08 19 Dec 2020 | 2 minutes 17 seconds |
Re-calibrating base error rates | 19:56:08 19 Dec 2020 | 19:56:13 19 Dec 2020 | 5 seconds |
Examining read alignment evidence | 19:56:13 19 Dec 2020 | 20:25:12 19 Dec 2020 | 28 minutes 59 seconds |
Polymorphism statistics | 20:25:12 19 Dec 2020 | 20:25:14 19 Dec 2020 | 2 seconds |
Output | 20:25:14 19 Dec 2020 | 20:26:19 19 Dec 2020 | 1 minute 5 seconds |
Total | 1 hour 57 minutes 2 seconds |