Closed JpGuegan closed 3 years ago
That's a nice idea. I think it's an exploratory analysis that might produce interesting results. But methodology-wise it's fairly avant garde, so I wouldn't want to have to defend that analysis to a journal.
Thanks for the reply. I should thus wait !
Hello,
I just have a foolish question concerning your reverseDecon function. Can I split my result from spatialdecon by condition (let's say by segments), apply the reverse deconvolution and look after for differentially expressed genes in each cell types using the coefs as input (limma or others) ?
data_annot$Segment <- as.factor(c("stroma_treated", "tumor_treated", "stroma_control","tumor_control"))
restils <- spatialdecon(norm = data_norm,
raw = data_raw,
bg = bg,
X = safeTME,
cell_counts = data_annot$AOINucleiCount,
is_pure_tumor = data_annot$istumor,
n_tumor_clusters = 2)
list_rdecon <- list()
for (i in 1:nlevels(data_annot$Segment)) { Sample <- data_annot %>% dplyr::filter(as.integer(Segment)==i) %>% rownames() x <- reverseDecon(norm = data_norm[,Sample], beta = restils$beta[,Sample]) list_rdecon[i]<-x }
Thanks for your help!