Benchmarking SignacX and SingleR with synovial flow cytometry data

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Mathew Chamberlain

2021-11-18

This vignette shows how to use Signac to annotate flow-sorted synovial cells by integrating SignacX with Seurat. We also compared Signac to another popular cell type annotation tool, SingleR. We start with raw counts.

Load data

Read the CEL-seq2 data.

ReadCelseq <- function(counts.file, meta.file) {
    E = suppressWarnings(readr::read_tsv(counts.file))
    gns <- E$gene
    E = E[, -1]
    E = Matrix::Matrix(as.matrix(E), sparse = TRUE)
    rownames(E) <- gns
    E
}

counts.file = "./fls/celseq_matrix_ru10_molecules.tsv.gz"
meta.file = "./fls/celseq_meta.immport.723957.tsv"

E = ReadCelseq(counts.file = counts.file, meta.file = meta.file)
M = suppressWarnings(readr::read_tsv(meta.file))

# filter data based on depth and number of genes detected
kmu = Matrix::colSums(E != 0)
kmu2 = Matrix::colSums(E)
E = E[, kmu > 200 & kmu2 > 500]

# filter by mitochondrial percentage
logik = grepl("^MT-", rownames(E))
MitoFrac = Matrix::colSums(E[logik, ])/Matrix::colSums(E) * 100
E = E[, MitoFrac < 20]

SingleR

require(SingleR)
data("hpca")
Q = SingleR(sc_data = E, ref_data = hpca$data, types = hpca$main_types, fine.tune = F, numCores = 4)
save(file = "fls/SingleR_Results.rda", Q)
True_labels = M$type[match(colnames(E), M$cell_name)]
saveRDS(True_labels, file = "fls/celltypes_amp_synovium_true.rds")

Seurat

Start with the standard pre-processing steps for a Seurat object.

library(Seurat)

Create a Seurat object, and then perform SCTransform normalization. Note:

You can use the legacy functions here (i.e., NormalizeData, ScaleData, etc.), use SCTransform or any other normalization method (including no normalization). We did not notice a significant difference in cell type annotations with different normalization methods.
We think that it is best practice to use SCTransform, but it is not a necessary step. Signac will work fine without it.

# load data
synovium <- CreateSeuratObject(counts = E, project = "FACs")

# run sctransform
synovium <- SCTransform(synovium, verbose = F)

Perform dimensionality reduction by PCA and UMAP embedding. Note:

Signac actually needs these functions since it uses the nearest neighbor graph generated by Seurat.

# These are now standard steps in the Seurat workflow for visualization and clustering
synovium <- RunPCA(synovium, verbose = FALSE)
synovium <- RunUMAP(synovium, dims = 1:30, verbose = FALSE)
synovium <- FindNeighbors(synovium, dims = 1:30, verbose = FALSE)

SignacX

library(SignacX)

Generate Signac labels for the Seurat object. Note:

Optionally, you can do parallel computing by setting num.cores > 1 in the Signac function.
Run time is ~10 minutes for <100,000 cells.

# Run Signac
labels <- Signac(synovium, num.cores = 4)
celltypes = GenerateLabels(labels, E = synovium)

Compare SignacX and SingleR with FACs labels

SignacX (rows are FACs labels, columns are SignacX)

	B	F	M	NonImmune	T	Unclassified
B	945	0	2	0	0	19
F	0	2218	10	223	0	58
M	1	28	891	18	0	96
T	4	0	0	0	1768	21

SingleR (rows are FACs labels, columns are SingleR)

	B	Chondr.	F	M	NK	NonImmune	T
B	958	1	0	6	1	0	0
F	2	1468	36	19	23	960	1
M	4	39	0	964	6	21	0
T	9	0	0	2	368	0	1414

Note:

These data were flow-sorted for CD3, and therefore lack NK cells. Signac detected no NK cells.
F = Fibroblasts; M = monocytes; T = T cells; B = B cells
Note that SingleR inaccurately annotated the majority of fibroblast cells as chondrocytes (Chondr.) and non immune cells, and also significantly identified NK cells (even though the data were flow-sorted for CD3, and thus lacked NK cells).

Signac accuracy

logik = xy != "Unclassified"
Signac_Accuracy = round(sum(xy[logik] == True_labels[logik])/sum(logik) * 100, 2)
Signac_Accuracy

## [1] 95.32

SingleR accuracy

SingleR_Accuracy = round(sum(xx == True_labels)/sum(logik) * 100, 2)
SingleR_Accuracy

## [1] 55.21

Save results

saveRDS(synovium, file = "synovium_signac.rds")
saveRDS(celltypes, file = "synovium_signac_celltypes.rds")

Session Info

## R version 4.0.3 (2020-10-10)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 18.04.5 LTS
## 
## Matrix products: default
## BLAS:   /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.7.1
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.7.1
## 
## locale:
##  [1] LC_CTYPE=en_US.UTF-8       LC_NUMERIC=C              
##  [3] LC_TIME=en_US.UTF-8        LC_COLLATE=en_US.UTF-8    
##  [5] LC_MONETARY=en_US.UTF-8    LC_MESSAGES=en_US.UTF-8   
##  [7] LC_PAPER=en_US.UTF-8       LC_NAME=C                 
##  [9] LC_ADDRESS=C               LC_TELEPHONE=C            
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C       
## 
## attached base packages:
## [1] stats     graphics  grDevices utils     datasets  methods   base     
## 
## loaded via a namespace (and not attached):
##  [1] compiler_4.0.3    magrittr_2.0.1    formatR_1.7       htmltools_0.5.1.1
##  [5] tools_4.0.3       yaml_2.2.1        stringi_1.5.3     rmarkdown_2.6    
##  [9] highr_0.8         knitr_1.30        stringr_1.4.0     digest_0.6.27    
## [13] xfun_0.20         rlang_0.4.10      evaluate_0.14

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