## ---- include = FALSE---------------------------------------------------------
knitr::opts_chunk$set(
collapse = TRUE,
comment = "#>"
)
## ----installation, eval=FALSE-------------------------------------------------
# if(!requireNamespace("BiocManager", quietly = TRUE))
# install.packages("BiocManager")
# BiocManager::install("SpatialDecon")
# BiocManager::install("GeoMxTools")
## ----setup--------------------------------------------------------------------
library(SpatialDecon)
library(GeomxTools)
## ----loaddata-----------------------------------------------------------------
data("nsclc")
dim(nsclc)
head(pData(nsclc))
nsclc@assayData$exprs[seq_len(5), seq_len(5)]
# better segment names:
sampleNames(nsclc) <-
paste0(nsclc$ROI, nsclc$AOI.name)
## ----derivebg-----------------------------------------------------------------
bg = derive_GeoMx_background(norm = nsclc@assayData$exprs_norm,
probepool = fData(nsclc)$Module,
negnames = c("NegProbe-CTP01", "NegProbe-Kilo"))
## ----showsafetme, fig.height=5, fig.width=10, fig.cap = "The safeTME cell profile matrix"----
data("safeTME")
data("safeTME.matches")
signif(safeTME[seq_len(3), seq_len(3)], 2)
heatmap(sweep(safeTME, 1, apply(safeTME, 1, max), "/"),
labRow = NA, margins = c(10, 5))
## ----downloadmatrix, fig.height=7, fig.width=10, fig.cap = "The Mouse Spleen profile matrix", eval=T----
mousespleen <- download_profile_matrix(species = "Mouse",
age_group = "Adult",
matrixname = "Spleen_MCA")
dim(mousespleen)
mousespleen[1:4,1:4]
head(cellGroups)
metadata
heatmap(sweep(mousespleen, 1, apply(mousespleen, 1, max), "/"),
labRow = NA, margins = c(10, 5), cexCol = 0.7)
## ----single cell data---------------------------------------------------------
data("mini_singleCell_dataset")
mini_singleCell_dataset$mtx@Dim # genes x cells
as.matrix(mini_singleCell_dataset$mtx)[1:4,1:4]
head(mini_singleCell_dataset$annots)
table(mini_singleCell_dataset$annots$LabeledCellType)
## ----creatematrix, fig.height=7, fig.width=10, fig.cap = "Custom profile matrix"----
custom_mtx <- create_profile_matrix(mtx = mini_singleCell_dataset$mtx, # cell x gene count matrix
cellAnnots = mini_singleCell_dataset$annots, # cell annotations with cell type and cell name as columns
cellTypeCol = "LabeledCellType", # column containing cell type
cellNameCol = "CellID", # column containing cell ID/name
matrixName = "custom_mini_colon", # name of final profile matrix
outDir = NULL, # path to desired output directory, set to NULL if matrix should not be written
normalize = FALSE, # Should data be normalized?
minCellNum = 5, # minimum number of cells of one type needed to create profile, exclusive
minGenes = 10, # minimum number of genes expressed in a cell, exclusive
scalingFactor = 5, # what should all values be multiplied by for final matrix
discardCellTypes = TRUE) # should cell types be filtered for types like mitotic, doublet, low quality, unknown, etc.
head(custom_mtx)
heatmap(sweep(custom_mtx, 1, apply(custom_mtx, 1, max), "/"),
labRow = NA, margins = c(10, 5), cexCol = 0.7)
## ----runiss-------------------------------------------------------------------
res = runspatialdecon(object = nsclc,
norm_elt = "exprs_norm",
raw_elt = "exprs",
X = safeTME,
align_genes = TRUE)
str(pData(res))
names(res@assayData)
## ----plotissres, fig.height = 5, fig.width = 8, fig.cap = "Cell abundance estimates"----
heatmap(t(res$beta), cexCol = 0.5, cexRow = 0.7, margins = c(10,7))
## ----showmatches--------------------------------------------------------------
str(safeTME.matches)
## ----runisstils---------------------------------------------------------------
# vector identifying pure tumor segments:
nsclc$istumor = nsclc$AOI.name == "Tumor"
# run spatialdecon with all the bells and whistles:
restils = runspatialdecon(object = nsclc,
norm_elt = "exprs_norm", # normalized data
raw_elt = "exprs", # expected background counts for every data point in norm
X = safeTME, # safeTME matrix, used by default
cellmerges = safeTME.matches, # safeTME.matches object, used by default
cell_counts = nsclc$nuclei, # nuclei counts, used to estimate total cells
is_pure_tumor = nsclc$istumor, # identities of the Tumor segments/observations
n_tumor_clusters = 5) # how many distinct tumor profiles to append to safeTME
str(pData(restils))
names(restils@assayData)
str(restils@experimentData@other)
## ----shownewX, fig.height=5, fig.width=8, fig.cap = "safeTME merged with newly-derived tumor profiles"----
heatmap(sweep(restils@experimentData@other$SpatialDeconMatrix, 1, apply(restils@experimentData@other$SpatialDeconMatrix, 1, max), "/"),
labRow = NA, margins = c(10, 5))
## ----barplot, fig.width=9, fig.height=6, fig.cap="Barplots of TIL abundance"----
# For reference, show the TILs color data object used by the plotting functions
# when safeTME has been used:
data("cellcols")
cellcols
# show just the TME segments, since that's where the immune cells are:
o = hclust(dist(t(restils$cell.counts$cell.counts)))$order
layout(mat = (matrix(c(1, 2), 1)), widths = c(7, 3))
TIL_barplot(t(restils$cell.counts$cell.counts[, o]), draw_legend = TRUE,
cex.names = 0.5)
# or the proportions of cells:
temp = replace(restils$prop_of_nontumor, is.na(restils$prop_of_nontumor), 0)
o = hclust(dist(temp[restils$AOI.name == "TME",]))$order
TIL_barplot(t(restils$prop_of_nontumor[restils$AOI.name == "TME",])[, o],
draw_legend = TRUE, cex.names = 0.75)
## ----florets, fig.width=8, fig.height=6, fig.cap = "TIL abundance plotted on PC space"----
# PCA of the normalized data:
pc = prcomp(t(log2(pmax(nsclc@assayData$exprs_norm, 1))))$x[, c(1, 2)]
# run florets function:
par(mar = c(5,5,1,1))
layout(mat = (matrix(c(1, 2), 1)), widths = c(6, 2))
florets(x = pc[, 1], y = pc[, 2],
b = t(restils$beta), cex = .5,
xlab = "PC1", ylab = "PC2")
par(mar = c(0,0,0,0))
frame()
legend("center", fill = cellcols[colnames(restils$beta)],
legend = colnames(restils$beta), cex = 0.7)
## ----collapse, fig.width=5, fig.height=5, fig.cap="Cell abundance estimates with related cell types collapsed"----
matching = list()
matching$myeloid = c( "macrophages", "monocytes", "mDCs")
matching$T.NK = c("CD4.T.cells","CD8.T.cells", "Treg", "NK")
matching$B = c("B")
matching$mast = c("mast")
matching$neutrophils = c("neutrophils")
matching$stroma = c("endothelial.cells", "fibroblasts")
collapsed = runCollapseCellTypes(object = restils,
matching = matching)
heatmap(t(collapsed$beta), cexRow = 0.85, cexCol = 0.75)
## ----appendtumor, fig.width = 10, fig.height= 5, fig.cap = "safeTME merged with newly-derived tumor profiles"----
pure.tumor.ids = res$AOI.name == "Tumor"
safeTME.with.tumor = runMergeTumorIntoX(object = nsclc,
norm_elt = "exprs_norm",
pure_tumor_ids = pure.tumor.ids,
X = safeTME,
K = 3)
heatmap(sweep(safeTME.with.tumor, 1, apply(safeTME.with.tumor, 1, max), "/"),
labRow = NA, margins = c(10, 5))
## ----reverse, fig.height=6, fig.width=6, fig.cap="Residuals from reverseDecon"----
rdecon = runReverseDecon(object = nsclc,
norm_elt = "exprs_norm",
beta = res$beta)
str(fData(rdecon))
names(rdecon@assayData)
# look at the residuals:
heatmap(pmax(pmin(rdecon@assayData$resids, 2), -2))
## ----reverse2, fig.height=6, fig.width=6, fig.cap="Genes' dependency on cell mixing"----
# look at the two metrics of goodness-of-fit:
plot(fData(rdecon)$cors, fData(rdecon)$resid.sd, col = 0)
showgenes = c("CXCL14", "LYZ", "FOXP3")
text(fData(rdecon)$cors[!rownames(fData(rdecon)) %in% showgenes],
fData(rdecon)$resid.sd[!rownames(fData(rdecon)) %in% showgenes],
setdiff(rownames(fData(rdecon)), showgenes), cex = 0.5)
text(fData(rdecon)$cors[rownames(fData(rdecon)) %in% showgenes], fData(rdecon)$resid.sd[rownames(fData(rdecon)) %in% showgenes],
showgenes, cex = 0.75, col = 2)
## ----sessioninfo--------------------------------------------------------------
sessionInfo()