A convenience function to identify samples with specific variants.
Usage
samples_with(cesa, any_of = NULL)
Arguments
- cesa
CESAnalysis
- any_of
Select samples with ANY of the given variant names/IDs, such as
c("8:142506482_C>G", "KRAS G12C"). When a gene has multiple transcripts in reference
data, you may wish to use full IDs, such as "KRAS_G12C_ENSP00000256078".