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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 | J21-E2_S135_R1_001.good.fq | 5,147,759 | 310,327,209 | 100.0% | 60.3 bases | 71 bases | 97.4% |
total | 5,147,759 | 310,327,209 | 100.0% | 60.3 bases | 71 bases | 97.4% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | W3110S.gb | 4,646,334 | 65.6 | 7.3 | 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 | 14825 |
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 | 195 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.006 |
reference sequence | pr(no read start) |
---|---|
W3110S.gb | 0.71111 |
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 | 04:34:45 11 Dec 2019 | 04:35:36 11 Dec 2019 | 51 seconds |
Read alignment to reference genome | 04:35:36 11 Dec 2019 | 04:41:23 11 Dec 2019 | 5 minutes 47 seconds |
Preprocessing alignments for candidate junction identification | 04:41:23 11 Dec 2019 | 04:42:34 11 Dec 2019 | 1 minute 11 seconds |
Preliminary analysis of coverage distribution | 04:42:34 11 Dec 2019 | 04:44:10 11 Dec 2019 | 1 minute 36 seconds |
Identifying junction candidates | 04:44:10 11 Dec 2019 | 04:44:12 11 Dec 2019 | 2 seconds |
Re-alignment to junction candidates | 04:44:12 11 Dec 2019 | 04:45:49 11 Dec 2019 | 1 minute 37 seconds |
Resolving best read alignments | 04:45:49 11 Dec 2019 | 04:47:28 11 Dec 2019 | 1 minute 39 seconds |
Creating BAM files | 04:47:28 11 Dec 2019 | 04:48:57 11 Dec 2019 | 1 minute 29 seconds |
Tabulating error counts | 04:48:57 11 Dec 2019 | 04:49:25 11 Dec 2019 | 28 seconds |
Re-calibrating base error rates | 04:49:25 11 Dec 2019 | 04:49:26 11 Dec 2019 | 1 second |
Examining read alignment evidence | 04:49:26 11 Dec 2019 | 04:57:29 11 Dec 2019 | 8 minutes 3 seconds |
Polymorphism statistics | 04:57:29 11 Dec 2019 | 04:57:30 11 Dec 2019 | 1 second |
Output | 04:57:30 11 Dec 2019 | 04:58:19 11 Dec 2019 | 49 seconds |
Total | 23 minutes 34 seconds |