breseq version 0.33.1 revision 8505477f25b3
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
read file | reads | bases | passed filters | average | longest | mapped | |
---|---|---|---|---|---|---|---|
errors | J8-E2_S111_R1_001.good.fq | 5,374,071 | 335,466,921 | 100.0% | 62.4 bases | 71 bases | 98.5% |
total | 5,374,071 | 335,466,921 | 100.0% | 62.4 bases | 71 bases | 98.5% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | W3110S.gb | 4,646,334 | 71.6 | 6.0 | 100.0% | Escherichia coli str. K-12 substr. W3110 DNA, complete genome. |
total | 4,646,334 | 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 | 52355 |
Coverage evenness (position-hash) score of junction candidates | ≥ 2 | ≥ 2 |
Test this many junction candidates (n). May be smaller if not enough passed the coverage evenness threshold | 100 ≤ n ≤ 5000 | 1212 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.038 |
reference sequence | pr(no read start) |
---|---|
W3110S.gb | 0.62238 |
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 |
Skew score of predicted junction (−log10 probability of unusual coverage evenness) must be | ≤ 0 |
Number of bases that at least one read must overlap each uniquely aligned side of a predicted junction | ≥ 6 |
option | value |
---|---|
Mode | Full Polymorphism |
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 | 2 |
Polymorphism frequency cutoff | 0.05 |
Polymorphism minimum variant coverage each strand | 2 |
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 | ≥3 bases |
Skip base substitutions when they create a homopolymer flanked on each side by | ≥5 bases |
program | version |
---|---|
bowtie2 | 2.3.4.1 |
R | 3.4.4 |
step | start | end | elapsed |
---|---|---|---|
Read and reference sequence file input | 04:59:51 11 Dec 2019 | 05:00:46 11 Dec 2019 | 55 seconds |
Read alignment to reference genome | 05:00:46 11 Dec 2019 | 05:06:48 11 Dec 2019 | 6 minutes 2 seconds |
Preprocessing alignments for candidate junction identification | 05:06:48 11 Dec 2019 | 05:08:05 11 Dec 2019 | 1 minute 17 seconds |
Preliminary analysis of coverage distribution | 05:08:05 11 Dec 2019 | 05:09:50 11 Dec 2019 | 1 minute 45 seconds |
Identifying junction candidates | 05:09:50 11 Dec 2019 | 05:10:10 11 Dec 2019 | 20 seconds |
Re-alignment to junction candidates | 05:10:10 11 Dec 2019 | 05:12:10 11 Dec 2019 | 2 minutes 0 seconds |
Resolving best read alignments | 05:12:10 11 Dec 2019 | 05:13:57 11 Dec 2019 | 1 minute 47 seconds |
Creating BAM files | 05:13:57 11 Dec 2019 | 05:15:34 11 Dec 2019 | 1 minute 37 seconds |
Tabulating error counts | 05:15:34 11 Dec 2019 | 05:16:06 11 Dec 2019 | 32 seconds |
Re-calibrating base error rates | 05:16:06 11 Dec 2019 | 05:16:06 11 Dec 2019 | 0 seconds |
Examining read alignment evidence | 05:16:06 11 Dec 2019 | 05:25:24 11 Dec 2019 | 9 minutes 18 seconds |
Polymorphism statistics | 05:25:24 11 Dec 2019 | 05:25:24 11 Dec 2019 | 0 seconds |
Output | 05:25:24 11 Dec 2019 | 05:26:19 11 Dec 2019 | 55 seconds |
Total | 26 minutes 28 seconds |