palimpsest_addSVcategoriesToVcf | R Documentation |
Function to add SV mutation categories to vcf
palimpsest_addSVcategoriesToVcf(
sv = sv,
type.col = "Type",
sample.col = "Sample",
CHROM_1.col = "CHROM",
CHROM_2.col = "CHROM",
POS_1.col = "POS",
POS_2.col = "POS",
resdir = resdir,
genome_build = "hg19"
)
sv |
vcf data frame containing the SVs |
type.col |
SV type description column name in mutation_data ["DEL","DUP","INV"] |
sample.col |
Sample column name in sv |
CHROM_1.col |
Start chromosome column name in sv |
CHROM_2.col |
End chromosome column name in sv |
POS_1.col |
Start position column name in sv |
POS_2.col |
End position column name in sv |
resdir |
Result directory |
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