mutation predictions | marginal predictions | summary statistics | genome diff | command line log
|
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 | ACB122_Van_A9_F116_I1_R1_S42_L001_R1_001.good.fq | 542,841 | 69,256,155 | 100.0% | 127.6 bases | 135 bases | 94.5% |
| errors | ACB122_Van_A9_F116_I1_R1_S42_L001_R2_001.good.fq | 542,841 | 69,258,176 | 100.0% | 127.6 bases | 135 bases | 91.5% |
| errors | ACB122_Van_A9_F116_I1_R1_S42_L002_R1_001.good.fq | 537,028 | 68,692,343 | 100.0% | 127.9 bases | 135 bases | 95.8% |
| errors | ACB122_Van_A9_F116_I1_R1_S42_L002_R2_001.good.fq | 537,028 | 68,692,456 | 100.0% | 127.9 bases | 135 bases | 93.9% |
| errors | ACB122_Van_A9_F116_I1_R1_S42_L003_R1_001.good.fq | 542,976 | 69,493,164 | 100.0% | 128.0 bases | 135 bases | 94.4% |
| errors | ACB122_Van_A9_F116_I1_R1_S42_L003_R2_001.good.fq | 542,976 | 69,492,786 | 100.0% | 128.0 bases | 135 bases | 92.4% |
| errors | ACB122_Van_A9_F116_I1_R1_S42_L004_R1_001.good.fq | 544,273 | 69,414,185 | 100.0% | 127.5 bases | 135 bases | 95.8% |
| errors | ACB122_Van_A9_F116_I1_R1_S42_L004_R2_001.good.fq | 544,273 | 69,415,158 | 100.0% | 127.5 bases | 135 bases | 94.0% |
| total | 4,334,236 | 553,714,423 | 100.0% | 127.8 bases | 135 bases | 94.0% |
| seq id | length | fit mean | fit dispersion | % mapped reads | description | ||
|---|---|---|---|---|---|---|---|
| coverage | distribution | ACB122 | 6,184,097 | 85.9 | 4.1 | 100.0% | tig00000001|arrow. |
| total | 6,184,097 | 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 | 2653 |
| 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 | 254 |
| Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.011 |
| reference sequence | pr(no read start) |
|---|---|
| ACB122 | 0.81698 |
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 | 0.75 |
| 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 | 2.2.6 |
| R | 3.4.4 |
| step | start | end | elapsed |
|---|---|---|---|
| Read and reference sequence file input | 22:07:15 01 May 2023 | 22:08:28 01 May 2023 | 1 minute 13 seconds |
| Read alignment to reference genome | 22:08:28 01 May 2023 | 22:18:38 01 May 2023 | 10 minutes 10 seconds |
| Preprocessing alignments for candidate junction identification | 22:18:38 01 May 2023 | 22:19:33 01 May 2023 | 55 seconds |
| Preliminary analysis of coverage distribution | 22:19:33 01 May 2023 | 22:22:06 01 May 2023 | 2 minutes 33 seconds |
| Identifying junction candidates | 22:22:06 01 May 2023 | 22:22:08 01 May 2023 | 2 seconds |
| Re-alignment to junction candidates | 22:22:08 01 May 2023 | 22:24:31 01 May 2023 | 2 minutes 23 seconds |
| Resolving best read alignments | 22:24:31 01 May 2023 | 22:25:49 01 May 2023 | 1 minute 18 seconds |
| Creating BAM files | 22:25:49 01 May 2023 | 22:28:08 01 May 2023 | 2 minutes 19 seconds |
| Tabulating error counts | 22:28:08 01 May 2023 | 22:28:57 01 May 2023 | 49 seconds |
| Re-calibrating base error rates | 22:28:57 01 May 2023 | 22:29:01 01 May 2023 | 4 seconds |
| Examining read alignment evidence | 22:29:01 01 May 2023 | 22:39:29 01 May 2023 | 10 minutes 28 seconds |
| Polymorphism statistics | 22:39:29 01 May 2023 | 22:39:29 01 May 2023 | 0 seconds |
| Output | 22:39:29 01 May 2023 | 22:39:55 01 May 2023 | 26 seconds |
| Total | 32 minutes 40 seconds | ||
