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breseq version 0.38.1
mutation predictions | marginal predictions | summary statistics | genome diff | command line log |
read file | reads | bases | passed filters | average | longest | mapped | |
---|---|---|---|---|---|---|---|
errors | 11109049673_S2060_Dung_Dnfi_c10.rawdata‡ | 963,957 | 192,791,400 | 98.3% | 200.0 bases | 200 bases | 94.3% |
total | 963,957 | 192,791,400 | 98.3% | 200.0 bases | 200 bases | 94.3% |
‡ Read and base numbers are after long reads in this file were split to exactly 200 bases (extra bases discarded)
seq id | length | fit mean | fit relative_variance | % mapped reads | description | ||
---|---|---|---|---|---|---|---|
coverage | distribution | NC_010473 | 4,686,137 | 37.4 | 1.3 | 100.0% | Escherichia coli str. K-12 substr. DH10B, complete sequence. |
total | 4,686,137 | 100.0% |
fit relative_variance 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 | 100039 |
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 | 864 |
Total length of all junction candidates (factor times the reference genome length) | ≤ 0.1 | 0.074 |
reference sequence | pr(no read start) |
---|---|
NC_010473 | 0.91267 |
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 | NO |
Skip indel polymorphisms in homopolymers runs of | ≥4 bases |
Skip base substitutions when they create a homopolymer flanked on each side by | OFF |
program | version |
---|---|
bowtie2 | 2.4.4 |
R | 4.1.1 |
step | start | end | elapsed |
---|---|---|---|
Read and reference sequence file input | 10:34:32 29 Sep 2024 | 10:34:52 29 Sep 2024 | 20 seconds |
Read alignment to reference genome | 10:34:52 29 Sep 2024 | 10:35:49 29 Sep 2024 | 57 seconds |
Preprocessing alignments for candidate junction identification | 10:35:49 29 Sep 2024 | 10:36:10 29 Sep 2024 | 21 seconds |
Preliminary analysis of coverage distribution | 10:36:10 29 Sep 2024 | 10:36:45 29 Sep 2024 | 35 seconds |
Identifying junction candidates | 10:36:45 29 Sep 2024 | 10:37:06 29 Sep 2024 | 21 seconds |
Re-alignment to junction candidates | 10:37:06 29 Sep 2024 | 10:37:21 29 Sep 2024 | 15 seconds |
Resolving best read alignments | 10:37:21 29 Sep 2024 | 10:37:52 29 Sep 2024 | 31 seconds |
Creating BAM files | 10:37:52 29 Sep 2024 | 10:38:19 29 Sep 2024 | 27 seconds |
Tabulating error counts | 10:38:19 29 Sep 2024 | 10:38:48 29 Sep 2024 | 29 seconds |
Re-calibrating base error rates | 10:38:48 29 Sep 2024 | 10:38:49 29 Sep 2024 | 1 second |
Examining read alignment evidence | 10:38:49 29 Sep 2024 | 10:42:46 29 Sep 2024 | 3 minutes 57 seconds |
Polymorphism statistics | 10:42:46 29 Sep 2024 | 10:42:47 29 Sep 2024 | 1 second |
Output | 10:42:47 29 Sep 2024 | 10:42:58 29 Sep 2024 | 11 seconds |
Output :: Mutation Prediction | 10:42:47 29 Sep 2024 | 10:42:51 29 Sep 2024 | 4 seconds |
Output :: Mutation Annotation | 10:42:51 29 Sep 2024 | 10:42:51 29 Sep 2024 | 0 seconds |
Total | 8 minutes 30 seconds |