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_22_S2355_L007_R1_001.good.fq | 169,318 | 22,112,745 | 100.0% | 130.6 bases | 150 bases | 95.1% |
errors | SvNSRound4_10_22_S2355_L007_R2_001.good.fq | 169,318 | 22,112,745 | 100.0% | 130.6 bases | 150 bases | 94.3% |
errors | SvNSRound4_10_22_S2355_L008_R1_001.good.fq | 104,442 | 13,717,084 | 100.0% | 131.3 bases | 150 bases | 94.6% |
errors | SvNSRound4_10_22_S2355_L008_R2_001.good.fq | 104,442 | 13,717,084 | 100.0% | 131.3 bases | 150 bases | 93.3% |
total | 547,520 | 71,659,658 | 100.0% | 130.9 bases | 150 bases | 94.4% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_000913_3_bme_pgi | 4,641,653 | 14.7 | 1.8 | 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 | 18527 |
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 | 25 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.002 |
reference sequence | pr(no read start) |
---|---|
NC_000913_3_bme_pgi | 0.94766 |
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 | 18:00:34 19 Dec 2020 | 18:01:07 19 Dec 2020 | 33 seconds |
Read alignment to reference genome | 18:01:08 19 Dec 2020 | 18:05:58 19 Dec 2020 | 4 minutes 50 seconds |
Preprocessing alignments for candidate junction identification | 18:05:58 19 Dec 2020 | 18:06:23 19 Dec 2020 | 25 seconds |
Preliminary analysis of coverage distribution | 18:06:23 19 Dec 2020 | 18:07:15 19 Dec 2020 | 52 seconds |
Identifying junction candidates | 18:07:15 19 Dec 2020 | 18:07:52 19 Dec 2020 | 37 seconds |
Re-alignment to junction candidates | 18:07:52 19 Dec 2020 | 18:08:51 19 Dec 2020 | 59 seconds |
Resolving best read alignments | 18:08:51 19 Dec 2020 | 18:09:27 19 Dec 2020 | 36 seconds |
Creating BAM files | 18:09:27 19 Dec 2020 | 18:10:12 19 Dec 2020 | 45 seconds |
Tabulating error counts | 18:10:12 19 Dec 2020 | 18:10:35 19 Dec 2020 | 23 seconds |
Re-calibrating base error rates | 18:10:35 19 Dec 2020 | 18:10:40 19 Dec 2020 | 5 seconds |
Examining read alignment evidence | 18:10:40 19 Dec 2020 | 18:16:33 19 Dec 2020 | 5 minutes 53 seconds |
Polymorphism statistics | 18:16:33 19 Dec 2020 | 18:16:34 19 Dec 2020 | 1 second |
Output | 18:16:34 19 Dec 2020 | 18:17:19 19 Dec 2020 | 45 seconds |
Total | 16 minutes 44 seconds |