#!/usr/bin/env Rscript
## Run on hpc
library(devtools)
load_all('/hpc/cog_bioinf/cuppen/project_data/Luan_projects/CHORD/scripts_main/hmfGeneAnnotation/')
args <- commandArgs(trailingOnly=T)
detGeneStatuses(
out.dir = args[1],
input.file.paths = c(germ_vcf=args[2], som_vcf=args[3], gene_cnv=args[4], cnv=args[5]),
sample.name = args[6],
java.path = args[7],
bed.file = args[8]
)
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