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_4_69_undiluted_S2271_L007_R1_001.good.fq | 226 | 29,127 | 100.0% | 128.9 bases | 129 bases | 1.3% |
errors | SvNSRound4_4_69_undiluted_S2271_L007_R2_001.good.fq | 226 | 29,127 | 100.0% | 128.9 bases | 129 bases | 0.9% |
errors | SvNSRound4_4_69_undiluted_S2271_L008_R1_001.good.fq | 151 | 19,195 | 100.0% | 127.1 bases | 129 bases | 6.0% |
errors | SvNSRound4_4_69_undiluted_S2271_L008_R2_001.good.fq | 151 | 19,195 | 100.0% | 127.1 bases | 129 bases | 6.0% |
total | 754 | 96,644 | 100.0% | 128.2 bases | 129 bases | 3.1% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_000913_3_bme_pgi | 4,641,653 | NA | NA | 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.
Insufficient coverage Reference sequence counted as entirely deleted due to low coverage. Try either the -t,--targeted-sequencing
or the -c,--contig-reference
option if you want mutations called for these reference sequences.
option | limit | actual |
---|---|---|
Number of alignment pairs examined for constructing junction candidates | ≤ 100000 | 0 |
Coverage evenness (position-hash) score of junction candidates | ≥ 2 | ≥ 0 |
Test this many junction candidates (n). May be smaller if not enough passed the coverage evenness threshold | 100 ≤ n ≤ 5000 | 0 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.000 |
reference sequence | pr(no read start) |
---|---|
NC_000913_3_bme_pgi | 1.00000 |
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 | 17:40:55 19 Dec 2020 | 17:40:59 19 Dec 2020 | 4 seconds |
Read alignment to reference genome | 17:41:00 19 Dec 2020 | 17:41:12 19 Dec 2020 | 12 seconds |
Preprocessing alignments for candidate junction identification | 17:41:12 19 Dec 2020 | 17:41:12 19 Dec 2020 | 0 seconds |
Preliminary analysis of coverage distribution | 17:41:12 19 Dec 2020 | 17:41:16 19 Dec 2020 | 4 seconds |
Identifying junction candidates | 17:41:16 19 Dec 2020 | 17:41:16 19 Dec 2020 | 0 seconds |
Re-alignment to junction candidates | 17:41:16 19 Dec 2020 | 17:41:16 19 Dec 2020 | 0 seconds |
Resolving best read alignments | 17:41:16 19 Dec 2020 | 17:41:17 19 Dec 2020 | 1 second |
Creating BAM files | 17:41:17 19 Dec 2020 | 17:41:17 19 Dec 2020 | 0 seconds |
Tabulating error counts | 17:41:17 19 Dec 2020 | 17:41:17 19 Dec 2020 | 0 seconds |
Re-calibrating base error rates | 17:41:17 19 Dec 2020 | 17:41:22 19 Dec 2020 | 5 seconds |
Examining read alignment evidence | 17:41:22 19 Dec 2020 | 17:41:28 19 Dec 2020 | 6 seconds |
Polymorphism statistics | 17:41:28 19 Dec 2020 | 17:41:29 19 Dec 2020 | 1 second |
Output | 17:41:29 19 Dec 2020 | 17:41:43 19 Dec 2020 | 14 seconds |
Total | 47 seconds |