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 | Plate-2-BOP-27-ACNB-ALE-1-flask-7_S25_L001_R1_001.good.fq | 185,530 | 23,358,177 | 100.0% | 125.9 bases | 149 bases | 94.7% |
errors | Plate-2-BOP-27-ACNB-ALE-1-flask-7_S25_L001_R2_001.good.fq | 185,530 | 23,028,528 | 100.0% | 124.1 bases | 149 bases | 98.0% |
errors | Plate-2-BOP-27-ACNB-ALE-1-flask-7_S25_L002_R1_001.good.fq | 145,010 | 18,146,741 | 100.0% | 125.1 bases | 149 bases | 94.2% |
errors | Plate-2-BOP-27-ACNB-ALE-1-flask-7_S25_L002_R2_001.good.fq | 145,010 | 17,869,624 | 100.0% | 123.2 bases | 149 bases | 97.5% |
errors | Plate-2-BOP-27-ACNB-ALE-1-flask-7_S25_L003_R1_001.good.fq | 167,187 | 20,954,974 | 100.0% | 125.3 bases | 149 bases | 94.5% |
errors | Plate-2-BOP-27-ACNB-ALE-1-flask-7_S25_L003_R2_001.good.fq | 167,187 | 20,646,811 | 100.0% | 123.5 bases | 149 bases | 97.9% |
errors | Plate-2-BOP-27-ACNB-ALE-1-flask-7_S25_L004_R1_001.good.fq | 142,773 | 17,822,793 | 100.0% | 124.8 bases | 149 bases | 94.1% |
errors | Plate-2-BOP-27-ACNB-ALE-1-flask-7_S25_L004_R2_001.good.fq | 142,773 | 17,561,564 | 100.0% | 123.0 bases | 149 bases | 97.3% |
total | 1,281,000 | 159,389,212 | 100.0% | 124.4 bases | 149 bases | 96.0% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_000913 | 4,641,652 | 33.0 | 2.4 | 100.0% | Escherichia coli str. K-12 substr. MG1655, complete genome. |
total | 4,641,652 | 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 | 15853 |
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 | 69 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.005 |
reference sequence | pr(no read start) |
---|---|
NC_000913 | 0.88225 |
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 | 13:06:03 29 Feb 2020 | 13:06:21 29 Feb 2020 | 18 seconds |
Read alignment to reference genome | 13:06:22 29 Feb 2020 | 13:08:44 29 Feb 2020 | 2 minutes 22 seconds |
Preprocessing alignments for candidate junction identification | 13:08:44 29 Feb 2020 | 13:09:02 29 Feb 2020 | 18 seconds |
Preliminary analysis of coverage distribution | 13:09:02 29 Feb 2020 | 13:09:35 29 Feb 2020 | 33 seconds |
Identifying junction candidates | 13:09:35 29 Feb 2020 | 13:10:09 29 Feb 2020 | 34 seconds |
Re-alignment to junction candidates | 13:10:09 29 Feb 2020 | 13:10:54 29 Feb 2020 | 45 seconds |
Resolving best read alignments | 13:10:54 29 Feb 2020 | 13:11:20 29 Feb 2020 | 26 seconds |
Creating BAM files | 13:11:20 29 Feb 2020 | 13:11:51 29 Feb 2020 | 31 seconds |
Tabulating error counts | 13:11:51 29 Feb 2020 | 13:12:02 29 Feb 2020 | 11 seconds |
Re-calibrating base error rates | 13:12:02 29 Feb 2020 | 13:12:05 29 Feb 2020 | 3 seconds |
Examining read alignment evidence | 13:12:05 29 Feb 2020 | 13:14:29 29 Feb 2020 | 2 minutes 24 seconds |
Polymorphism statistics | 13:14:29 29 Feb 2020 | 13:14:29 29 Feb 2020 | 0 seconds |
Output | 13:14:30 29 Feb 2020 | 13:14:40 29 Feb 2020 | 10 seconds |
Total | 8 minutes 35 seconds |