breseq version 0.35.7 revision b7a44cd89118
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
read file | reads | bases | passed filters | average | longest | mapped | |
---|---|---|---|---|---|---|---|
errors | G2_CCGTCC_L007_R1_001 | 503,257 | 63,410,382 | 100.0% | 126.0 bases | 126 bases | 98.1% |
errors | G2_CCGTCC_L007_R2_001 | 502,544 | 63,320,544 | 99.9% | 126.0 bases | 126 bases | 97.9% |
total | 1,005,801 | 126,730,926 | 99.9% | 126.0 bases | 126 bases | 98.0% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | ADP1-WT | 3,600,835 | 35.1 | 1.7 | 100.0% | Acinetobacter sp. ADP1 chromosome, complete genome. |
junction‑only | pYTK001_with_tdk_kan | 3,341 | NA | NA | 0.0% | . | |
total | 3,600,835 | 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 | 336 |
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 | 14 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.001 |
reference sequence | pr(no read start) |
---|---|
ADP1-WT | 0.88368 |
pYTK001_with_tdk_kan | NA |
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 |
Minimum probablilty assigned that no mapped read will start at a given position and strand for junction prediction | 0.1 |
Junction allow suboptimal matches | FALSE |
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 | 0.8 |
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 | 4.0.0 |
step | start | end | elapsed |
---|---|---|---|
Read and reference sequence file input | 07:49:52 20 Jul 2021 | 07:53:33 20 Jul 2021 | 3 minutes 41 seconds |
Read alignment to reference genome | 07:56:12 20 Jul 2021 | 07:59:13 20 Jul 2021 | 3 minutes 1 second |
Preprocessing alignments for candidate junction identification | 07:59:13 20 Jul 2021 | 08:00:21 20 Jul 2021 | 1 minute 8 seconds |
Preliminary analysis of coverage distribution | 08:00:21 20 Jul 2021 | 08:12:20 20 Jul 2021 | 11 minutes 59 seconds |
Identifying junction candidates | 08:12:20 20 Jul 2021 | 08:12:20 20 Jul 2021 | 0 seconds |
Re-alignment to junction candidates | 08:12:20 20 Jul 2021 | 08:13:04 20 Jul 2021 | 44 seconds |
Resolving best read alignments | 08:13:04 20 Jul 2021 | 08:15:08 20 Jul 2021 | 2 minutes 4 seconds |
Creating BAM files | 08:15:08 20 Jul 2021 | 08:15:32 20 Jul 2021 | 24 seconds |
Tabulating error counts | 08:15:32 20 Jul 2021 | 08:16:42 20 Jul 2021 | 1 minute 10 seconds |
Re-calibrating base error rates | 08:16:42 20 Jul 2021 | 08:16:44 20 Jul 2021 | 2 seconds |
Examining read alignment evidence | 08:16:44 20 Jul 2021 | 09:19:11 20 Jul 2021 | 1 hour 2 minutes 27 seconds |
Polymorphism statistics | 09:19:11 20 Jul 2021 | 09:19:11 20 Jul 2021 | 0 seconds |
Output | 09:19:11 20 Jul 2021 | 09:19:30 20 Jul 2021 | 19 seconds |
Output :: Mutation Prediction | 09:19:11 20 Jul 2021 | 09:19:12 20 Jul 2021 | 1 second |
Output :: Mutation Annotation | 09:19:12 20 Jul 2021 | 09:19:19 20 Jul 2021 | 7 seconds |
Total | 1 hour 27 minutes 7 seconds |