CoFAST: PBMC scRNA-seq data coembedding

Load and view data

We demonstrate the use of CoFAST to PBMC3k data that are in the SeuratData package, which can be downloaded to the current working path by the following command:

set.seed(2024) # set a random seed for reproducibility.
library(Seurat)
pbmc3k <- SeuratData::LoadData("pbmc3k")
## filter the seurat_annotation is NA
idx <- which(!is.na(pbmc3k$seurat_annotations))
pbmc3k <- pbmc3k[,idx]
pbmc3k

The package can be loaded with the command:

library(ProFAST) # load the package of FAST method
library(Seurat)

Preprocessing

First, we normalize the data.

pbmc3k <- NormalizeData(pbmc3k)

Then, we select the variable genes.

pbmc3k <- FindVariableFeatures(pbmc3k)

Coembedding using non-centered factor model

We introduce how to use the non-centered factor model (NCFM) to perform coembedding for this scRNA-seq data. First, we determine the dimension of coembeddings. Here, we use the parallel analysis method to select the dimension.

dat_cor <- diagnostic.cor.eigs(pbmc3k)
q_est <- attr(dat_cor, "q_est")
cat("q_est = ", q_est, '\n')

Subsequently, we calculate coembeddings by utilizing NCFM, and observe that the reductions field acquires an additional component named ncfm.

pbmc3k <- NCFM(pbmc3k, q = q_est)
pbmc3k

Downstream analysis

In the following, we show how to find the signature genes based on comebeddings. First, we calculate the distance matrix.

pbmc3k <- pdistance(pbmc3k, reduction = "ncfm")

Next, we find the signature genes for each cell type

print(table(pbmc3k$seurat_annotations))
Idents(pbmc3k) <- pbmc3k$seurat_annotations
df_sig_list <- find.signature.genes(pbmc3k)
str(df_sig_list)

Then, we obtain the top five signature genes and organize them into a data.frame. The colname distance means the distance between gene (i.e., VPREB3) and cells with the specific cell type (i.e., B cell), which is calculated based on the coembedding of genes and cells in the coembedding space. The distance is smaller, the association between gene and the cell type is stronger. The colname expr.prop represents the expression proportion of the gene (i.e., VPREB3) within the cell type (i.e., B cell). The colname label means the cell types and colname gene denotes the gene name. By the data.frame object, we know VPREB3 is the one of the top signature gene of B cell.

dat <- get.top.signature.dat(df_sig_list, ntop = 5, expr.prop.cutoff = 0.1)
head(dat)

Next, we calculate the UMAP projections of coembeddings of cells and the selected signature genes.

pbmc3k <- coembedding_umap(
  pbmc3k, reduction = "ncfm", reduction.name = "UMAP",
  gene.set = unique(dat$gene))

Furthermore, we visualize the cells and top five signature genes of B cell in the UMAP space of coembedding. We observe that the UMAP projections of the five signature genes are near to B cells, which indicates these genes are enriched in B cells.

## choose beutifual colors
cols_cluster <- c("black", PRECAST::chooseColors(palettes_name = "Light 13", n_colors = 9, plot_colors = TRUE))
p1 <- coembed_plot(
   pbmc3k, reduction = "UMAP",
   gene_txtdata = subset(dat, label=='B'), 
   cols=cols_cluster,pt_text_size = 3)
p1

Then, we visualize the cells and top five signature genes of all involved cell types in the UMAP space of coembedding. We observe that the UMAP projections of the five signature genes are near to the corresponding cell type, which indicates these genes are enriched in the corresponding cells.

p2 <- coembed_plot(
   pbmc3k, reduction = "UMAP",
   gene_txtdata = dat, cols=cols_cluster,
   pt_text_size = 3)
p2

In addtion, we can fully take advantages of the visualization functions in Seurat package for visualization. The following is an example that visualizes the cell types on the UMAP space.

cols_type <- cols_cluster[-1]
names(cols_type)<-  sort(levels(Idents(pbmc3k)))
DimPlot(pbmc3k, reduction = 'UMAP', cols=cols_type)

Then, there is another example that we plot the two signature genes of B cell on UMAP space, in which we observed the high expression in B cells in constrast to other cell types.

FeaturePlot(pbmc3k, reduction = 'UMAP', features = c("CD79A", "VPREB3"))

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