View source: R/annotate_VCF_functions.R
add_ID_cats_ToVCF | R Documentation |
Adds Indel mutation categories to a VCF.
add_ID_cats_ToVCF(
vcf = NULL,
ref_fasta = NULL,
palimpdir_man = NA,
genome = NA,
GRCh37 = FALSE
)
vcf |
VCF to which Indel mutation categories are to be added. |
ref_fasta |
Path to fasta file for reference genome of choice (e.g. hg19 genome). |
palimpdir_man |
Path to palimpsest directory entered manually. Must contain the "exec" folder. |
genome |
Taken from annotate_VCF function. |
GRCh37 |
Logical indicating whether reference fasta file is GRCh37 (i.e. no 'chr' prefixes). |
vcf <- add_ID_cats_ToVCF(vcf = vcf,ref_fasta = ref_fasta)
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.