library(monocle)
library(HSMMSingleCell)
context("markerDiffTable is functioning properly")
pd <- new("AnnotatedDataFrame", data = HSMM_sample_sheet)
fd <- new("AnnotatedDataFrame", data = HSMM_gene_annotation)
HSMM <- newCellDataSet(as.matrix(HSMM_expr_matrix), phenoData = pd, featureData = fd)
HSMM <- newCellDataSet(as(umi_matrix, "sparseMatrix"),
phenoData = pd,
featureData = fd,
lowerDetectionLimit = 0.5,
expressionFamily = negbinomial.size())
cellranger_pipestance_path <- "/path/to/your/pipeline/output/directory"
gbm <- load_cellranger_matrix(cellranger_pipestance_path)
gbm_cds <- newCellDataSet(exprs(gbm),
phenoData = new("AnnotatedDataFrame", data = pData(gbm)),
phenoData = new("AnnotatedDataFrame", data = fData(gbm)),
lowerDetectionLimit = 0.5,
expressionFamily = negbinomial.size())
HSMM <- detectGenes(HSMM, min_expr = 0.1)
expressed_genes <- row.names(subset(fData(HSMM), num_cells_expressed >= 10))
valid_cells <- row.names(subset(pData(HSMM),
Cells.in.Well == 1 &
Control == FALSE &
Clump == FALSE &
Debris == FALSE &
Mapped.Fragments > 1000000))
HSMM <- HSMM[,valid_cells]
pData(HSMM)$Total_mRNAs <- Matrix::colSums(exprs(HSMM))
HSMM <- HSMM[,pData(HSMM)$Total_mRNAs < 1e6]
upper_bound <- 10^(mean(log10(pData(HSMM)$Total_mRNAs)) +
2*sd(log10(pData(HSMM)$Total_mRNAs)))
lower_bound <- 10^(mean(log10(pData(HSMM)$Total_mRNAs)) -
2*sd(log10(pData(HSMM)$Total_mRNAs)))
HSMM <- HSMM[,pData(HSMM)$Total_mRNAs > lower_bound &
pData(HSMM)$Total_mRNAs < upper_bound]
HSMM <- detectGenes(HSMM, min_expr = 0.1)
# Log-transform each value in the expression matrix.
L <- log(exprs(HSMM[expressed_genes,]))
# Standardize each gene, so that they are all on the same scale,
# Then melt the data with plyr so we can plot it easily
melted_dens_df <- melt(Matrix::t(scale(Matrix::t(L))))
# Plot the distribution of the standardized gene expression values.
qplot(value, geom = "density", data = melted_dens_df) +
stat_function(fun = dnorm, size = 0.5, color = 'red') +
xlab("Standardized log(FPKM)") +
ylab("Density")
MYF5_id <- row.names(subset(fData(HSMM), gene_short_name == "MYF5"))
ANPEP_id <- row.names(subset(fData(HSMM), gene_short_name == "ANPEP"))
cth <- newCellTypeHierarchy()
cth <- addCellType(cth, "Myoblast", classify_func = function(x) { x[MYF5_id,] >= 1 })
cth <- addCellType(cth, "Fibroblast", classify_func = function(x)
{ x[MYF5_id,] < 1 & x[ANPEP_id,] > 1 })
HSMM <- classifyCells(HSMM, cth, 0.1)
test_that("markerDiffTable works properly in vignette",
expect_error(markerDiffTable(HSMM[expressed_genes,],
cth,
residualModelFormulaStr = "~Media + num_genes_expressed",
cores = 1), NA))
test_that("markerDiffTable works when 'balanced set to true'",
expect_error(markerDiffTable(HSMM[expressed_genes,],
cth,
balanced = TRUE,
residualModelFormulaStr = "~Media + num_genes_expressed",
cores = 1), NA))
test_that("markerDiffTable works when 'verbose set to true'",
expect_error(markerDiffTable(HSMM[expressed_genes,],
cth,
verbose = TRUE,
residualModelFormulaStr = "~Media + num_genes_expressed",
cores = 1), NA))
test_that("markerDiffTable throws error if cds is not of type 'CellDataSet'",
expect_error(markerDiffTable(cth,
cth,
balanced = TRUE,
residualModelFormulaStr = "~Media + num_genes_expressed",
cores = 1), "Error cds is not of type 'CellDataSet'"))
test_that("markerDiffTable throws error if cds is not of type 'CellDataSet'",
expect_error(markerDiffTable(HSMM[expressed_genes,],
HSMM[expressed_genes],
balanced = TRUE,
residualModelFormulaStr = "~Media + num_genes_expressed",
cores = 1), "Error cth is not of type 'CellTypeHierarchy'"))
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.