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 | ALE-13_S13_L001_R1_001.good.fq | 331,019 | 46,819,834 | 100.0% | 141.4 bases | 149 bases | 93.9% |
errors | ALE-13_S13_L001_R2_001.good.fq | 331,019 | 46,626,376 | 100.0% | 140.9 bases | 149 bases | 94.6% |
errors | ALE-13_S13_L002_R1_001.good.fq | 322,573 | 45,532,762 | 100.0% | 141.2 bases | 149 bases | 95.2% |
errors | ALE-13_S13_L002_R2_001.good.fq | 322,573 | 45,385,475 | 100.0% | 140.7 bases | 149 bases | 95.1% |
errors | ALE-13_S13_L003_R1_001.good.fq | 337,213 | 47,561,782 | 100.0% | 141.0 bases | 149 bases | 95.1% |
errors | ALE-13_S13_L003_R2_001.good.fq | 337,213 | 47,386,467 | 100.0% | 140.5 bases | 149 bases | 95.6% |
errors | ALE-13_S13_L004_R1_001.good.fq | 308,851 | 43,554,966 | 100.0% | 141.0 bases | 149 bases | 95.0% |
errors | ALE-13_S13_L004_R2_001.good.fq | 308,851 | 43,414,919 | 100.0% | 140.6 bases | 149 bases | 94.7% |
total | 2,599,312 | 366,282,581 | 100.0% | 140.9 bases | 149 bases | 94.9% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_002947 | 6,181,873 | 54.2 | 2.2 | 100.0% | Pseudomonas putida KT2440 chromosome, complete genome. |
total | 6,181,873 | 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 | 51714 |
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 | 437 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.022 |
reference sequence | pr(no read start) |
---|---|
NC_002947 | 0.83412 |
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 | 01:11:36 18 Feb 2020 | 01:12:15 18 Feb 2020 | 39 seconds |
Read alignment to reference genome | 01:12:15 18 Feb 2020 | 01:17:53 18 Feb 2020 | 5 minutes 38 seconds |
Preprocessing alignments for candidate junction identification | 01:17:53 18 Feb 2020 | 01:18:30 18 Feb 2020 | 37 seconds |
Preliminary analysis of coverage distribution | 01:18:30 18 Feb 2020 | 01:19:58 18 Feb 2020 | 1 minute 28 seconds |
Identifying junction candidates | 01:19:58 18 Feb 2020 | 01:25:53 18 Feb 2020 | 5 minutes 55 seconds |
Re-alignment to junction candidates | 01:25:53 18 Feb 2020 | 01:27:38 18 Feb 2020 | 1 minute 45 seconds |
Resolving best read alignments | 01:27:38 18 Feb 2020 | 01:28:35 18 Feb 2020 | 57 seconds |
Creating BAM files | 01:28:35 18 Feb 2020 | 01:29:57 18 Feb 2020 | 1 minute 22 seconds |
Tabulating error counts | 01:29:57 18 Feb 2020 | 01:30:23 18 Feb 2020 | 26 seconds |
Re-calibrating base error rates | 01:30:23 18 Feb 2020 | 01:30:26 18 Feb 2020 | 3 seconds |
Examining read alignment evidence | 01:30:26 18 Feb 2020 | 01:44:15 18 Feb 2020 | 13 minutes 49 seconds |
Polymorphism statistics | 01:44:15 18 Feb 2020 | 01:44:17 18 Feb 2020 | 2 seconds |
Output | 01:44:17 18 Feb 2020 | 01:47:43 18 Feb 2020 | 3 minutes 26 seconds |
Total | 36 minutes 7 seconds |