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-56_S56_L001_R1_001.good.fq | 366,259 | 52,253,550 | 100.0% | 142.7 bases | 149 bases | 92.2% |
errors | ALE-56_S56_L001_R2_001.good.fq | 366,259 | 51,924,348 | 100.0% | 141.8 bases | 149 bases | 93.3% |
errors | ALE-56_S56_L002_R1_001.good.fq | 359,721 | 51,246,217 | 100.0% | 142.5 bases | 149 bases | 93.6% |
errors | ALE-56_S56_L002_R2_001.good.fq | 359,721 | 50,980,695 | 100.0% | 141.7 bases | 149 bases | 93.7% |
errors | ALE-56_S56_L003_R1_001.good.fq | 370,286 | 52,693,949 | 100.0% | 142.3 bases | 149 bases | 93.3% |
errors | ALE-56_S56_L003_R2_001.good.fq | 370,286 | 52,374,254 | 100.0% | 141.4 bases | 149 bases | 94.3% |
errors | ALE-56_S56_L004_R1_001.good.fq | 345,663 | 49,191,680 | 100.0% | 142.3 bases | 149 bases | 93.4% |
errors | ALE-56_S56_L004_R2_001.good.fq | 345,663 | 48,931,673 | 100.0% | 141.6 bases | 149 bases | 93.3% |
total | 2,883,858 | 409,596,366 | 100.0% | 142.0 bases | 149 bases | 93.4% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_002947 | 6,181,873 | 62.2 | 2.3 | 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 | 81630 |
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 | 651 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.032 |
reference sequence | pr(no read start) |
---|---|
NC_002947 | 0.81901 |
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 | ≤ 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 | 2.3.4.1 |
R | 3.4.4 |
step | start | end | elapsed |
---|---|---|---|
Read and reference sequence file input | 09:06:42 18 Feb 2020 | 09:07:25 18 Feb 2020 | 43 seconds |
Read alignment to reference genome | 09:07:25 18 Feb 2020 | 09:13:52 18 Feb 2020 | 6 minutes 27 seconds |
Preprocessing alignments for candidate junction identification | 09:13:52 18 Feb 2020 | 09:14:33 18 Feb 2020 | 41 seconds |
Preliminary analysis of coverage distribution | 09:14:33 18 Feb 2020 | 09:16:09 18 Feb 2020 | 1 minute 36 seconds |
Identifying junction candidates | 09:16:09 18 Feb 2020 | 09:32:21 18 Feb 2020 | 16 minutes 12 seconds |
Re-alignment to junction candidates | 09:32:21 18 Feb 2020 | 09:34:24 18 Feb 2020 | 2 minutes 3 seconds |
Resolving best read alignments | 09:34:24 18 Feb 2020 | 09:35:26 18 Feb 2020 | 1 minute 2 seconds |
Creating BAM files | 09:35:26 18 Feb 2020 | 09:36:56 18 Feb 2020 | 1 minute 30 seconds |
Tabulating error counts | 09:36:56 18 Feb 2020 | 09:37:26 18 Feb 2020 | 30 seconds |
Re-calibrating base error rates | 09:37:26 18 Feb 2020 | 09:37:29 18 Feb 2020 | 3 seconds |
Examining read alignment evidence | 09:37:29 18 Feb 2020 | 09:43:14 18 Feb 2020 | 5 minutes 45 seconds |
Polymorphism statistics | 09:43:14 18 Feb 2020 | 09:43:15 18 Feb 2020 | 1 second |
Output | 09:43:15 18 Feb 2020 | 09:43:57 18 Feb 2020 | 42 seconds |
Total | 37 minutes 15 seconds |