Description Usage Arguments Value
View source: R/call_resistance.R
Command line version of the website application Takes as input a VCF, varscan tab or fasta file. The program assumes variant files are generated relative to Merlin strain. Fasta files if not Whole Genome, or not aligned / assembled relative to Merlin are Processed using MAFFT & snp-sites. In this case the output files are returned to your working directory.
1 2 3 4 5 6 | call_resistance(
infile = system.file("testdata", "A10.vcf", package = "cmvdrg"),
all_mutations = FALSE,
inc_anecdotal = FALSE,
outdir = ""
)
|
infile |
the input fasta, vcf or varscan.tab file |
all_mutations |
when FALSE only recognised resistant variants present are returned. |
inc_anecdotal |
include anectodat database entries in returned results? |
outdir |
for fasta input files intermediate alignment fasta & vcf files are generated, this defines the directory they are saved to. "out.fasta" "out.vcf" |
A data.frame containing resistance information for variants identified
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