Reads in a directory of VCF files and converts them into a single dataframe
arrange_data(
vardir,
reference_fasta,
annotated = "yes",
ntlist = c("A", "G", "T", "C", "-"),
verbose = FALSE
)
A large dataframe containing information from all input VCF files
Directory path containing vcf files
Reference fasta file used for alignment
Whether the VCF files are annotated using snpeff "yes" or "no" (default "yes")
Nucleotides (default A, T, G, C) used for finding multiple alt alleles
set verbosity of the vcfR commands