Description Usage Arguments Value
View source: R/mutationCalling.R
Identifies relevant mitochondrial somatic variants from raw counts of nucleotide frequencies. Applies two sets of filters: In the first step, filters on coverage and minimum allele frequency to exclude potentially noisy variants; in the second step, filters against a blacklist of variants that were observed in several individuals and that therefore are unlikely to represent true somatic variants (e.g. RNA editing events). These blacklists are created using mutationCallsFromCohort
1 2 3 4 5 6 7 8 9 10 11 12 | mutationCallsFromBlacklist(
BaseCounts,
lim.cov = 20,
min.af = 0.2,
min.num.samples = 0.01 * length(BaseCounts),
min.af.universal = min.af,
universal.var.cells = 0.95 * length(BaseCounts),
blacklists.use = blacklists,
max.var.na = 0.5,
max.cell.na = 0.95,
...
)
|
BaseCounts |
A list of base call matrices (one matrix per cell) as produced by |
lim.cov |
Minimal coverage required per cell for a cell to be classified as covered |
min.af |
Minimal allele frequency for a cell to be classified as mutant |
min.num.samples |
Minimal number of cells required to be classified as covered and mutant according to the thresholds set in |
min.af.universal |
Minimal allele frequency for a cell to be classified as mutant, in the context of removing universal variants. Defaults to |
universal.var.cells |
Maximum number of cells required to be classified as mutant according to the threshold set in |
max.var.na |
Final filtering step: Remove all mutations with no coverage in more than this fraction of cells |
max.cell.na |
Final filtering step: Remove all cells with no coverage in more than this fraction of mutations |
... |
Parameters passed to |
blacklists |
Blacklists to use **explanations ben** |
An object of class mutationCalls
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