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library(ctl)
# The genotypes.csv file containing the genotype matrix is stored individuals (rows) x genetic marker (columns):
args = commandArgs(trailingOnly=TRUE)
if (length(args)==0) {
stop("Argument for the geno and pheno file location is required", call.=FALSE)
} else {
# default output file
geno_file = args[1]
pheno_file = args[2]
}
genotypes <- read.csv(geno_file,row.names=1, header=FALSE, sep="\t")
# The phenotypes.csv file containing individuals (rows) x traits (columns) measurements:
traits <- read.csv(pheno_file,row.names=1, header=FALSE, sep="\t")
ctls <- CTLscan(geno,traits,strategy=input$strategy,
nperm=input$nperms,parametric =input$parametric,
nthreads=6,verbose=TRUE)
#output matrix significant CTL interactions with 4 columns: trait, marker, trait, lod
sign <- CTLsignificant(ctls,significance = input$significance)
# add plots
json_data <- list(significance=signs,
images=lists("image_1":"image_location"),
network_figure_location="/location")
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