breseq version 0.35.4 revision f352f80f4bc9
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
read file | reads | bases | passed filters | average | longest | mapped | |
---|---|---|---|---|---|---|---|
errors | SvNSRound3_8_57POP_S2495_L007_R1_001.good.fq | 592,788 | 88,870,067 | 100.0% | 149.9 bases | 150 bases | 98.0% |
errors | SvNSRound3_8_57POP_S2495_L007_R2_001.good.fq | 592,788 | 88,870,067 | 100.0% | 149.9 bases | 150 bases | 95.5% |
errors | SvNSRound3_8_57POP_S2495_L008_R1_001.good.fq | 388,163 | 58,194,294 | 100.0% | 149.9 bases | 150 bases | 97.9% |
errors | SvNSRound3_8_57POP_S2495_L008_R2_001.good.fq | 388,163 | 58,194,294 | 100.0% | 149.9 bases | 150 bases | 95.2% |
total | 1,961,902 | 294,128,722 | 100.0% | 149.9 bases | 150 bases | 96.7% |
seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_000913_3_hsa_tpiA | 4,641,634 | 61.5 | 3.5 | 100.0% | Escherichia coli str. K-12 substr. MG1655, H. sapien tpiA gene, complete genome. |
total | 4,641,634 | 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 | 8874 |
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 | 143 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.010 |
reference sequence | pr(no read start) |
---|---|
NC_000913_3_hsa_tpiA | 0.83734 |
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 | ≤ 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 | 2.2.6 |
R | 3.4.4 |
step | start | end | elapsed |
---|---|---|---|
Read and reference sequence file input | 18:17:47 19 Dec 2020 | 18:19:36 19 Dec 2020 | 1 minute 49 seconds |
Read alignment to reference genome | 18:19:37 19 Dec 2020 | 18:34:27 19 Dec 2020 | 14 minutes 50 seconds |
Preprocessing alignments for candidate junction identification | 18:34:27 19 Dec 2020 | 18:35:49 19 Dec 2020 | 1 minute 22 seconds |
Preliminary analysis of coverage distribution | 18:35:49 19 Dec 2020 | 18:39:13 19 Dec 2020 | 3 minutes 24 seconds |
Identifying junction candidates | 18:39:13 19 Dec 2020 | 18:39:16 19 Dec 2020 | 3 seconds |
Re-alignment to junction candidates | 18:39:16 19 Dec 2020 | 18:43:08 19 Dec 2020 | 3 minutes 52 seconds |
Resolving best read alignments | 18:43:08 19 Dec 2020 | 18:45:14 19 Dec 2020 | 2 minutes 6 seconds |
Creating BAM files | 18:45:14 19 Dec 2020 | 18:48:42 19 Dec 2020 | 3 minutes 28 seconds |
Tabulating error counts | 18:48:42 19 Dec 2020 | 18:50:00 19 Dec 2020 | 1 minute 18 seconds |
Re-calibrating base error rates | 18:50:00 19 Dec 2020 | 18:50:04 19 Dec 2020 | 4 seconds |
Examining read alignment evidence | 18:50:04 19 Dec 2020 | 19:49:40 19 Dec 2020 | 59 minutes 36 seconds |
Polymorphism statistics | 19:49:40 19 Dec 2020 | 19:49:41 19 Dec 2020 | 1 second |
Output | 19:49:41 19 Dec 2020 | 19:50:16 19 Dec 2020 | 35 seconds |
Total | 1 hour 32 minutes 28 seconds |