Nothing
setpath.wrapper <-
function(d1,d2,pathwaygenes,pathwaynames,M=1,transform=NULL,minalpha=NULL,normalize=TRUE,pvalue="chisq",npermutations=10000)
{
K = length(pathwaynames)
results = matrix(NA,K,2*(M+1)+2)
dimnames(results)[[1]] = pathwaynames
dimnames(results)[[2]] = c("n.genes",paste("alpha.0",1:M,sep="."),"T.0",paste("alpha.0",1:M,sep="."),"T.0","pval")
# make sure gene names align:
if(!identical(dimnames(d1)[[2]],dimnames(d2)[[2]]))
{
stop("d1 and d2 have different feature (column) names.")
}
# now run the method on each pathway:
for(k in 1:K)
{
# check formatting of pathways:
missinggenes = setdiff(pathwaygenes[[k]],dimnames(d1)[[2]])
if(length(missinggenes)>0)
{
warning(c("The following pathway genes are missing from the dataset:",missinggenes))
pathwaygenes[[k]] = intersect(pathwaygenes[[k]],dimnames(d1)[[2]])
}
temp = setpath(d1[,pathwaygenes[[k]]],d2[,pathwaygenes[[k]]],M=M,transform=transform,verbose=TRUE,minalpha=minalpha,normalize=normalize,pvalue=pvalue,npermutations=npermutations)
results[k,] = c(length(pathwaygenes[[k]]),temp$stats[,1],temp$stats[,2],temp$pval)
}
return(results)
}
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