View source: R/TrinucleotideVariantsLib.R
dnvTabToTNVcatalogue | R Documentation |
This function takes as input a list of double nucleotide variants (DNVs), and computes a list of trinucleotide variants (TNVs) finding which DNVs are next to each other. It then returns the annotated TNVs and the TNV catalogues. The trinucleotide mutations considered are only those where all three bases change, i.e. TTT>AAA but not TTT>ATA.
dnvTabToTNVcatalogue(dnvtab)
dnvtab |
requires columns Sample, Chrom, Pos, Ref, Alt, with Ref and Alt of length 2 |
list of TNVs and TNV catalogue
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