test_mat <- read_tsv("bulk_mat_mouse.tsv") %>%
as.data.frame() %>%
tibble::column_to_rownames("gene_symbol")
test_that("mmcp_counter works", {
res <- deconvolute_mmcp_counter(test_mat)
assert("matrix dimensions consistent", ncol(res) == ncol(test_mat))
})
test_that("seqimmucc works", {
res <- deconvolute_seqimmucc(test_mat, algorithm = "LLSR")
assert("matrix dimensions consistent", ncol(res) == ncol(test_mat))
})
test_that("DCQ works", {
res <- deconvolute_dcq(test_mat)
assert("matrix dimensions consistent", ncol(res) == ncol(test_mat))
})
test_that("BASE works", {
res <- deconvolute_base_algorithm(test_mat, n_permutations = 5)
assert("matrix dimensions consistent", ncol(res) == ncol(test_mat))
})
test_that("DCQ works without reducing cell types", {
res <- deconvolute_dcq(test_mat, combine_cells = FALSE, n_repeats = 5)
assert("matrix dimensions consistent", ncol(res) == ncol(test_mat))
})
test_that("generic deconvolution works for all methods", {
lapply(deconvolution_methods_mouse, function(method) {
print(paste0("method is ", method))
res <- deconvolute_mouse(test_mat, method, algorithm = "LLSR")
# matrix has the 'cell type' column -> +1
assert("matrix dimensions consistent", ncol(res) == ncol(test_mat) + 1)
assert("cell type column exists", colnames(res)[1] == "cell_type")
assert("sample names consistent with input", colnames(res)[-1] == colnames(test_mat))
})
})
# test_that("mouse gene names can be converted into their human orthologus, and vice versa", {
# test_mat_newGenes <- convert_human_mouse_genes(test_mat[1:1000, ], convert_to = "human")
# assert("matrix dimensions consistent", ncol(test_mat_newGenes) == ncol(test_mat))
#
# test_mat_human <- read_tsv("bulk_mat.tsv") %>%
# as.data.frame() %>%
# tibble::column_to_rownames("gene_symbol")
# test_mat_newGenes <- convert_human_mouse_genes(test_mat_human[1:1000, ], convert_to = "mouse")
# assert("matrix dimensions consistent", ncol(test_mat_newGenes) == ncol(test_mat_human))
# })
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