filterSNV {mutSignatures} | R Documentation |
Filter Single Nucleotide Variants.
Description
Remove entries corresponding to non-SNV, such as insertions and deletions.
Usage
filterSNV(dataSet, seq_colNames)
Arguments
dataSet |
data.frame including variant information |
seq_colNames |
character vector with the names of the columns storing variant data |
Details
This function is part of the user-interface set of tools included in mutSignatures. This is an exported function.
Value
a filtered data.frame only including SNVs
Author(s)
Damiano Fantini, damiano.fantini@gmail.com
References
More information and examples about mutational signature analysis can be found here:
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GitHub Repo: https://github.com/dami82/mutSignatures/
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More info and examples about the mutSignatures R library: https://www.data-pulse.com/dev_site/mutsignatures/
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Sci Rep paper, introducing mutS: https://www.nature.com/articles/s41598-020-75062-0/
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Oncogene paper, Mutational Signatures Operative in Bladder Cancer: https://www.nature.com/articles/s41388-017-0099-6
Examples
x <- mutSignatures:::getTestRunArgs("filterSNV")
nrow(x)
y <- mutSignatures::filterSNV(dataSet = x,
seq_colNames = c("REF", "ALT"))
nrow(y)