Example of running spASE on some simulated data.
library(spASE)
# Null simulation parameters ngenes <- 100 numi <- 5 p <- 0.5 phi <- 0.2 a <- p*(1-phi)/phi b <- (1-phi)*(1-p)/phi # Simulate raw ASE data in a square coords <- expand.grid(seq(1,5,0.1), seq(1,5,0.1)) npixels <- nrow(coords) matrix1 <- matrix(nrow = ngenes, ncol = npixels) matrix2 <- matrix(nrow = ngenes, ncol = npixels) for (i in 1:ngenes) { lambda.p <- rbeta(npixels, a, b) matrix1[i,] <- rbinom(npixels, size=numi, prob=lambda.p) matrix2[i,] <- numi - matrix1[i,] } rownames(matrix1) <- rownames(matrix2) <- paste0('gene', seq(1,ngenes)) colnames(matrix1) <- colnames(matrix2) <- paste0('pixel', seq(1,npixels)) covariates <- cbind(data.frame(pixel = paste0('pixel',seq(1,npixels))), coords) results <- spase(matrix1, matrix2, covariates, cores=1)
# view the results data frame results$result %>% arrange(qval)
# plot the results for the first gene plotSpase(matrix1, matrix2, covariates, results, genes = 'gene28', coords=coords)
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