CiteFuse: getting started
26 October 2021
1 Introduction
CiteFuse is a computational framework that implements a suite of methods and tools for CITE-seq data from pre-processing through to integrative analytics. This includes doublet detection, network-based modality integration, cell type clustering, differential RNA and protein expression analysis, ADT evaluation, ligand-receptor interaction analysis, and interactive web-based visualisation of the analyses. This vignette demonstrates the usage of CiteFuse on a subset data of CITE-seq data from human PBMCs as an example (Mimitou et al., 2019).
First, install CiteFuse using BiocManager.
if (!requireNamespace("BiocManager", quietly = TRUE)) {
install.packages("BiocManager")
}
BiocManager::install("CiteFuse")library(CiteFuse)
library(scater)
library(SingleCellExperiment)
library(DT)data("CITEseq_example", package = "CiteFuse")
names(CITEseq_example)
#> [1] "RNA" "ADT" "HTO"
lapply(CITEseq_example, dim)
#> $RNA
#> [1] 19521 500
#>
#> $ADT
#> [1] 49 500
#>
#> $HTO
#> [1] 4 500Here, we start from a list of three matrices of unique molecular identifier (UMI), antibody derived tags (ADT) and hashtag oligonucleotide (HTO) count, which have common cell names. There are 500 cells in our subsetted dataset. And characteristically of CITE-seq data, the matrices are matched, meaning that for any given cell we know the expression level of their RNA transcripts (genome-wide) and its corresponding cell surface protein expression. The preprocessing function will utilise the three matrices and its common cell names to create a SingleCellExperiment object, which stores RNA data in an assay and ADT and HTO data within in the altExp slot.
sce_citeseq <- preprocessing(CITEseq_example)
sce_citeseq
#> class: SingleCellExperiment
#> dim: 19521 500
#> metadata(0):
#> assays(1): counts
#> rownames(19521): hg19_AL627309.1 hg19_AL669831.5 ... hg19_MT-ND6
#> hg19_MT-CYB
#> rowData names(0):
#> colnames(500): AAGCCGCGTTGTCTTT GATCGCGGTTATCGGT ... TTGGCAACACTAGTAC
#> GCTGCGAGTTGTGGCC
#> colData names(0):
#> reducedDimNames(0):
#> mainExpName: NULL
#> altExpNames(2): ADT HTO2 Detecting both cross- and within-sample doublets using CiteFuse
2.1 HTO Normalisation and Visualisation
The function normaliseExprs is used to scale the alternative expression. Here, we used it to perform log-transformation of the HTO count, by setting transform = "log".
sce_citeseq <- normaliseExprs(sce = sce_citeseq,
altExp_name = "HTO",
transform = "log")Then we can perform dimension reduction on the HTO count by using runTSNE or runUMAP, then use visualiseDim function to visualise the reduced dimension plot. Our CITE-seq dataset contain data from four samples that were pooled before sequencing. The samples were multiplexed through cell hashing (Stoekius et al., 2018). The four clusters observed on reduced dimension plots equate to the four different samples.
sce_citeseq <- scater::runTSNE(sce_citeseq,
altexp = "HTO",
name = "TSNE_HTO",
pca = TRUE)
visualiseDim(sce_citeseq,
dimNames = "TSNE_HTO") + labs(title = "tSNE (HTO)")
sce_citeseq <- scater::runUMAP(sce_citeseq,
altexp = "HTO",
name = "UMAP_HTO")
visualiseDim(sce_citeseq,
dimNames = "UMAP_HTO") + labs(title = "UMAP (HTO)")
2.2 Doublet identification step 1: cross-sample doublet detection
An important step in single cell data analysis is the removal of doublets. Doublets form as a result of co-encapsulation of cells within a droplet, leading to a hybrid transcriptome from two or more cells. In CiteFuse, we implement a step-wise doublet detection approach to remove doublets. We first identify the cross-sample doublets via the crossSampleDoublets function.
sce_citeseq <- crossSampleDoublets(sce_citeseq)
#> number of iterations= 20
#> number of iterations= 24
#> number of iterations= 46
#> number of iterations= 50The results of the cross sample doublets are then saved in colData as doubletClassify_between_label and doubletClassify_between_class.
table(sce_citeseq$doubletClassify_between_label)
#>
#> 1 2 3 4
#> 115 121 92 129
#> doublet/multiplet
#> 43
table(sce_citeseq$doubletClassify_between_class)
#>
#> Singlet doublet/multiplet
#> 457 43We can then highlight the cross-sample doublets in our tSNE plot of HTO count.
visualiseDim(sce_citeseq,
dimNames = "TSNE_HTO",
colour_by = "doubletClassify_between_label")
Furthermore, plotHTO function allows us to plot the pairwise scatter HTO count. Any cells that show co-expression of orthologocal HTOs (red) are considered as doublets.
plotHTO(sce_citeseq, 1:4)
2.3 Doublet identification step 1: within-sample doublet detection
We then identify the within-sample doublets via the withinSampleDoublets function.
sce_citeseq <- withinSampleDoublets(sce_citeseq,
minPts = 10)The results of the cross sample doublets are then saved in the colData as doubletClassify_within_label and doubletClassify_within_class.
table(sce_citeseq$doubletClassify_within_label)
#>
#> Doublets(Within)_1 Doublets(Within)_2 Doublets(Within)_3 Doublets(Within)_4
#> 3 7 4 6
#> NotDoublets(Within)
#> 480
table(sce_citeseq$doubletClassify_within_class)
#>
#> Doublet Singlet
#> 20 480Again, we can visualise the within-sample doublets in our tSNE plot.
visualiseDim(sce_citeseq,
dimNames = "TSNE_HTO",
colour_by = "doubletClassify_within_label")
Finally, we can filter out the doublet cells (both within and between batches) for the downstream analysis.
sce_citeseq <- sce_citeseq[, sce_citeseq$doubletClassify_within_class == "Singlet" & sce_citeseq$doubletClassify_between_class == "Singlet"]
sce_citeseq
#> class: SingleCellExperiment
#> dim: 19521 437
#> metadata(3): doubletClassify_between_threshold
#> doubletClassify_between_resultsMat doubletClassify_within_resultsMat
#> assays(1): counts
#> rownames(19521): hg19_AL627309.1 hg19_AL669831.5 ... hg19_MT-ND6
#> hg19_MT-CYB
#> rowData names(0):
#> colnames(437): GATCGCGGTTATCGGT GGCTGGTAGAGGTTAT ... TTGGCAACACTAGTAC
#> GCTGCGAGTTGTGGCC
#> colData names(5): doubletClassify_between_label
#> doubletClassify_between_class nUMI doubletClassify_within_label
#> doubletClassify_within_class
#> reducedDimNames(2): TSNE_HTO UMAP_HTO
#> mainExpName: NULL
#> altExpNames(2): ADT HTO3 Clustering
3.1 Performing SNF
The first step of analysis is to integrate the RNA and ADT matrix. We use a popular integration algorithm called similarity network fusion (SNF) to integrate the multiomic data.
sce_citeseq <- scater::logNormCounts(sce_citeseq)
sce_citeseq <- normaliseExprs(sce_citeseq, altExp_name = "ADT", transform = "log")
system.time(sce_citeseq <- CiteFuse(sce_citeseq))
#> Calculating affinity matrix
#> Performing SNF
#> user system elapsed
#> 5.885 0.076 5.964We now proceed with the fused matrix, which is stored as SNF_W in our sce_citeseq object.
3.2 Performing spectral clustering
CiteFuse implements two different clustering algorithms on the fused matrix, spectral clustering and Louvain clustering. First, we perform spectral clustering with sufficient numbers of K and use the eigen values to determine the optimal number of clusters.
SNF_W_clust <- spectralClustering(metadata(sce_citeseq)[["SNF_W"]], K = 20)
#> Computing Spectral Clustering
plot(SNF_W_clust$eigen_values)
which.max(abs(diff(SNF_W_clust$eigen_values)))
#> [1] 5Using the optimal cluster number defined from the previous step, we can now use the spectralClutering function to cluster the single cells by specifying the number of clusters in K. The function takes a cell-to-cell similarity matrix as an input. We have already created the fused similarity matrix from CiteFuse. Since the CiteFuse function creates and stores the similarity matries from ADT and RNA expression, as well the fused matrix, we can use these two to compare the clustering outcomes by data modality.
SNF_W_clust <- spectralClustering(metadata(sce_citeseq)[["SNF_W"]], K = 5)
#> Computing Spectral Clustering
sce_citeseq$SNF_W_clust <- as.factor(SNF_W_clust$labels)
SNF_W1_clust <- spectralClustering(metadata(sce_citeseq)[["ADT_W"]], K = 5)
#> Computing Spectral Clustering
sce_citeseq$ADT_clust <- as.factor(SNF_W1_clust$labels)
SNF_W2_clust <- spectralClustering(metadata(sce_citeseq)[["RNA_W"]], K = 5)
#> Computing Spectral Clustering
sce_citeseq$RNA_clust <- as.factor(SNF_W2_clust$labels)3.3 Visualisation
The outcome of the clustering can be easily visualised on a reduced dimensions plot by highlighting the points by cluster label.
sce_citeseq <- reducedDimSNF(sce_citeseq,
method = "tSNE",
dimNames = "tSNE_joint")
g1 <- visualiseDim(sce_citeseq, dimNames = "tSNE_joint", colour_by = "SNF_W_clust") +
labs(title = "tSNE (SNF clustering)")
g2 <- visualiseDim(sce_citeseq, dimNames = "tSNE_joint", colour_by = "ADT_clust") +
labs(title = "tSNE (ADT clustering)")
g3 <- visualiseDim(sce_citeseq, dimNames = "tSNE_joint", colour_by = "RNA_clust") +
labs(title = "tSNE (RNA clustering)")
library(gridExtra)
grid.arrange(g3, g2, g1, ncol = 2)
The expression of genes and proteins can be visualised by changing the colour_by parameter to assess the clusters. As an example, we highlight the plot by the RNA and ADT expression level of CD8.
g1 <- visualiseDim(sce_citeseq, dimNames = "tSNE_joint",
colour_by = "hg19_CD8A",
data_from = "assay",
assay_name = "logcounts") +
labs(title = "tSNE: hg19_CD8A (RNA expression)")
g2 <- visualiseDim(sce_citeseq,dimNames = "tSNE_joint",
colour_by = "CD8",
data_from = "altExp",
altExp_assay_name = "logcounts") +
labs(title = "tSNE: CD8 (ADT expression)")
grid.arrange(g1, g2, ncol = 2)
3.4 Louvain clustering
As well as spectral clustering, CiteFuse can implement Louvain clustering if users wish to use another clustering method. We use the igraph package, and any community detection algorithms available in their package can be selected by changing the method parameter.
SNF_W_louvain <- igraphClustering(sce_citeseq, method = "louvain")
table(SNF_W_louvain)
#> SNF_W_louvain
#> 1 2 3 4 5 6 7
#> 88 137 65 32 51 28 36
sce_citeseq$SNF_W_louvain <- as.factor(SNF_W_louvain)
visualiseDim(sce_citeseq, dimNames = "tSNE_joint", colour_by = "SNF_W_louvain") +
labs(title = "tSNE (SNF louvain clustering)")
visualiseKNN(sce_citeseq, colour_by = "SNF_W_louvain")
4 Differential Expression Analysis
4.1 Exploration of feature expression
CiteFuse has a wide range of visualisation tools to facilitate exploratory analysis of CITE-seq data. The visualiseExprs function is an easy-to-use function to generate boxplots, violinplots, jitter plots, density plots, and pairwise scatter/density plots of genes and proteins expressed in the data. The plots can be grouped by using the cluster labels stored in the sce_citeseq object.
visualiseExprs(sce_citeseq,
plot = "boxplot",
group_by = "SNF_W_louvain",
feature_subset = c("hg19_CD2", "hg19_CD4", "hg19_CD8A", "hg19_CD19"))
visualiseExprs(sce_citeseq,
plot = "violin",
group_by = "SNF_W_louvain",
feature_subset = c("hg19_CD2", "hg19_CD4", "hg19_CD8A", "hg19_CD19"))
visualiseExprs(sce_citeseq,
plot = "jitter",
group_by = "SNF_W_louvain",
feature_subset = c("hg19_CD2", "hg19_CD4", "hg19_CD8A", "hg19_CD19"))
visualiseExprs(sce_citeseq,
plot = "density",
group_by = "SNF_W_louvain",
feature_subset = c("hg19_CD2", "hg19_CD4", "hg19_CD8A", "hg19_CD19"))
visualiseExprs(sce_citeseq,
altExp_name = "ADT",
group_by = "SNF_W_louvain",
plot = "violin", n = 5)
visualiseExprs(sce_citeseq, altExp_name = "ADT",
plot = "jitter",
group_by = "SNF_W_louvain",
feature_subset = c("CD2", "CD8", "CD4", "CD19"))
visualiseExprs(sce_citeseq, altExp_name = "ADT",
plot = "density",
group_by = "SNF_W_louvain",
feature_subset = c("CD2", "CD8", "CD4", "CD19"))
visualiseExprs(sce_citeseq, altExp_name = "ADT",
plot = "pairwise",
feature_subset = c("CD4", "CD8"))
#> number of iterations= 12
#> number of iterations= 21
visualiseExprs(sce_citeseq, altExp_name = "ADT",
plot = "pairwise",
feature_subset = c("CD45RA", "CD4", "CD8"),
threshold = rep(4, 3))
4.2 Perform DE Analysis with Wilcoxon Rank Sum test
CiteFuse also calculates differentially expressed (DE) genes through the DEgenes function. The cluster grouping to use must be specified in the group parameter. If altExp_name is not specified, RNA expression will be used as the default expression matrix.
Results form the DE analysis is stored in sce_citeseq as DE_res_RNA_filter and DE_res_ADT_filter for RNA and ADT expression, respectively.
4.2.1 For RNA expression
# DE will be performed for RNA if altExp_name = "none"
sce_citeseq <- DEgenes(sce_citeseq,
altExp_name = "none",
group = sce_citeseq$SNF_W_louvain,
return_all = TRUE,
exprs_pct = 0.5)
sce_citeseq <- selectDEgenes(sce_citeseq,
altExp_name = "none")
datatable(format(do.call(rbind, metadata(sce_citeseq)[["DE_res_RNA_filter"]]),
digits = 2))4.2.2 For ADT count
sce_citeseq <- DEgenes(sce_citeseq,
altExp_name = "ADT",
group = sce_citeseq$SNF_W_louvain,
return_all = TRUE,
exprs_pct = 0.5)
sce_citeseq <- selectDEgenes(sce_citeseq,
altExp_name = "ADT")
datatable(format(do.call(rbind, metadata(sce_citeseq)[["DE_res_ADT_filter"]]),
digits = 2))4.3 Visualising DE Results
The DE genes can be visualised with the DEbubblePlot and DEcomparisonPlot. In each case, the gene names must first be extracted from the DE result objects.
4.3.1 circlepackPlot
The circlepackPlot takes a list of all DE genes from RNA and ADT DE analysis and will plot only the top most significant DE genes to plot.
rna_DEgenes <- metadata(sce_citeseq)[["DE_res_RNA_filter"]]
adt_DEgenes <- metadata(sce_citeseq)[["DE_res_ADT_filter"]]
rna_DEgenes <- lapply(rna_DEgenes, function(x){
x$name <- gsub("hg19_", "", x$name)
x})
DEbubblePlot(list(RNA = rna_DEgenes, ADT = adt_DEgenes))
4.3.2 DEcomparisonPlot
For the DEcomparisonPlot, as well as a list containing the DE genes for RNA and ADT, a feature_list specifying the genes and proteins of interest is required.
rna_list <- c("hg19_CD4",
"hg19_CD8A",
"hg19_HLA-DRB1",
"hg19_ITGAX",
"hg19_NCAM1",
"hg19_CD27",
"hg19_CD19")
adt_list <- c("CD4", "CD8", "MHCII (HLA-DR)", "CD11c", "CD56", "CD27", "CD19")
rna_DEgenes_all <- metadata(sce_citeseq)[["DE_res_RNA"]]
adt_DEgenes_all <- metadata(sce_citeseq)[["DE_res_ADT"]]
feature_list <- list(RNA = rna_list, ADT = adt_list)
de_list <- list(RNA = rna_DEgenes_all, ADT = adt_DEgenes_all)
DEcomparisonPlot(de_list = de_list,
feature_list = feature_list)
5 ADT Importance Evaluation
An important evaluation in CITE-seq data analysis is to assess the quality of each ADT and to evaluate the contribution of ADTs towards clustering outcome. CiteFuse calculates the relative importance of ADT towards clustering outcome by using a random forest model. The higher the score of an ADT, the greater its importance towards the final clustering outcome.
set.seed(2020)
sce_citeseq <- importanceADT(sce_citeseq,
group = sce_citeseq$SNF_W_louvain,
subsample = TRUE)
visImportance(sce_citeseq, plot = "boxplot")
visImportance(sce_citeseq, plot = "heatmap")
sort(metadata(sce_citeseq)[["importanceADT"]], decreasing = TRUE)[1:20]
#> CD27 CD8 CD4 PECAM (CD31)
#> 41.032868 35.381533 33.494609 12.263987
#> CD5 CD28 CD7 CD11b
#> 12.201304 12.123428 11.791693 10.808128
#> IL7Ralpha (CD127) MHCII (HLA-DR) CD2 CD44
#> 9.868645 8.657011 8.589313 8.466849
#> CD366 (tim3) HLA-A,B,C CD11c CD3
#> 5.893551 5.832131 4.933470 4.517884
#> CD45RA CD26 (Adenosine) CD69 PD-1 (CD279)
#> 4.016464 3.776677 3.734701 3.508469The importance scores can be visualised in a boxplot and heatmap. Our evaluation of ADT importance show that unsurprisingly CD4 and CD8 are the top two discriminating proteins in PBMCs.
Let us try clustering with only ADTs with a score greater than 5.
subset_adt <- names(which(metadata(sce_citeseq)[["importanceADT"]] > 5))
subset_adt
#> [1] "CD11b" "CD2" "CD27"
#> [4] "CD28" "CD366 (tim3)" "CD4"
#> [7] "CD44" "CD5" "CD7"
#> [10] "CD8" "HLA-A,B,C" "IL7Ralpha (CD127)"
#> [13] "MHCII (HLA-DR)" "PECAM (CD31)"
system.time(sce_citeseq <- CiteFuse(sce_citeseq,
ADT_subset = subset_adt,
metadata_names = c("W_SNF_adtSubset1",
"W_ADT_adtSubset1",
"W_RNA")))
#> Calculating affinity matrix
#> Performing SNF
#> user system elapsed
#> 3.844 0.020 3.864
SNF_W_clust_adtSubset1 <- spectralClustering(metadata(sce_citeseq)[["W_SNF_adtSubset1"]], K = 5)
#> Computing Spectral Clustering
sce_citeseq$SNF_W_clust_adtSubset1 <- as.factor(SNF_W_clust_adtSubset1$labels)
library(mclust)
adjustedRandIndex(sce_citeseq$SNF_W_clust_adtSubset1, sce_citeseq$SNF_W_clust)
#> [1] 0.8499764When we compare between the two clustering outcomes, we find that the adjusted rand index is approximately 0.93, where a value of 1 denotes complete concordance.
6 Gene - ADT network
The geneADTnetwork function plots an interaction network between genes identified from the DE analysis. The nodes denote proteins and RNA whilst the edges denote positive and negative correlation in expression.
RNA_feature_subset <- unique(as.character(unlist(lapply(rna_DEgenes_all, "[[", "name"))))
ADT_feature_subset <- unique(as.character(unlist(lapply(adt_DEgenes_all, "[[", "name"))))
geneADTnetwork(sce_citeseq,
RNA_feature_subset = RNA_feature_subset,
ADT_feature_subset = ADT_feature_subset,
cor_method = "pearson",
network_layout = igraph::layout_with_fr)
#> IGRAPH 78721ab UN-B 72 134 --
#> + attr: name (v/c), label (v/c), class (v/c), type (v/l), shape (v/c),
#> | color (v/c), size (v/n), label.cex (v/n), label.color (v/c), value
#> | (e/n), color (e/c), weights (e/n)
#> + edges from 78721ab (vertex names):
#> [1] RNA_hg19_CD8A --ADT_CD4 RNA_hg19_CCL5 --ADT_CD4 RNA_hg19_GNLY --ADT_CD4
#> [4] RNA_hg19_KLRD1--ADT_CD4 RNA_hg19_GZMB --ADT_CD4 RNA_hg19_CST7 --ADT_CD4
#> [7] RNA_hg19_NKG7 --ADT_CD4 RNA_hg19_CTSW --ADT_CD4 RNA_hg19_LTB --ADT_CD27
#> [10] RNA_hg19_TCF7 --ADT_CD27 RNA_hg19_RPL32--ADT_CD27 RNA_hg19_IL7R --ADT_CD27
#> [13] RNA_hg19_RPL13--ADT_CD27 RNA_hg19_RPL37--ADT_CD27 RNA_hg19_RPS8 --ADT_CD27
#> [16] RNA_hg19_RPL11--ADT_CD27 RNA_hg19_CD27 --ADT_CD27 RNA_hg19_RPS12--ADT_CD27
#> + ... omitted several edges7 RNA Ligand - ADT Receptor Analysis
With the advent of CITE-seq, we can now predict ligand-receptor interactions by using cell surface protein expression. CiteFuse implements a ligandReceptorTest to find ligand receptor interactions between sender and receiver cells. Importantly, the ADT count is used to predict receptor expression within receiver cells. Note that the setting altExp_name = "RNA" would enable users to predict ligand-receptor interaction from RNA expression only.
data("lr_pair_subset", package = "CiteFuse")
head(lr_pair_subset)
#> [,1] [,2]
#> [1,] "hg19_IL17RA" "CD45"
#> [2,] "hg19_FAS" "CD11b"
#> [3,] "hg19_GZMK" "CD62L"
#> [4,] "hg19_CD40LG" "CD11b"
#> [5,] "hg19_FLT3LG" "CD62L"
#> [6,] "hg19_GZMA" "CD19"
sce_citeseq <- normaliseExprs(sce = sce_citeseq,
altExp_name = "ADT",
transform = "zi_minMax")
sce_citeseq <- normaliseExprs(sce = sce_citeseq,
altExp_name = "none",
exprs_value = "logcounts",
transform = "minMax")
sce_citeseq <- ligandReceptorTest(sce = sce_citeseq,
ligandReceptor_list = lr_pair_subset,
cluster = sce_citeseq$SNF_W_louvain,
RNA_exprs_value = "minMax",
use_alt_exp = TRUE,
altExp_name = "ADT",
altExp_exprs_value = "zi_minMax",
num_permute = 1000)
#> 100 ......200 ......300 ......400 ......500 ......600 ......700 ......800 ......900 ......1000 ......visLigandReceptor(sce_citeseq,
type = "pval_heatmap",
receptor_type = "ADT")
visLigandReceptor(sce_citeseq,
type = "pval_dotplot",
receptor_type = "ADT")
visLigandReceptor(sce_citeseq,
type = "group_network",
receptor_type = "ADT")
visLigandReceptor(sce_citeseq,
type = "group_heatmap",
receptor_type = "ADT")
visLigandReceptor(sce_citeseq,
type = "lr_network",
receptor_type = "ADT")
8 Between-sample analysis
Lastly, we will jointly analyse the current PBMC CITE-seq data, taken from healthy human donors, and another subset of CITE-seq data from patients with cutaneous T-cell lymphoma (CTCL), again from Mimitou et al. (2019). The data sce_ctcl_subset provided in our CiteFuse package already contains the clustering information.
data("sce_ctcl_subset", package = "CiteFuse")To visualise and compare gene or protein expression data, we can use visualiseExprsList function.
visualiseExprsList(sce_list = list(control = sce_citeseq,
ctcl = sce_ctcl_subset),
plot = "boxplot",
altExp_name = "none",
exprs_value = "logcounts",
feature_subset = c("hg19_S100A10", "hg19_CD8A"),
group_by = c("SNF_W_louvain", "SNF_W_louvain"))
visualiseExprsList(sce_list = list(control = sce_citeseq,
ctcl = sce_ctcl_subset),
plot = "boxplot",
altExp_name = "ADT",
feature_subset = c("CD19", "CD8"),
group_by = c("SNF_W_louvain", "SNF_W_louvain"))
We can then perform differential expression analysis of the RNA expression level across the two clusters that have high CD19 expression in ADT.
de_res <- DEgenesCross(sce_list = list(control = sce_citeseq,
ctcl = sce_ctcl_subset),
colData_name = c("SNF_W_louvain", "SNF_W_louvain"),
group_to_test = c("2", "6"))
de_res_filter <- selectDEgenes(de_res = de_res)
de_res_filter
#> $control
#> stats.W pval p.adjust meanExprs.1 meanExprs.2
#> hg19_GNLY 28.0 6.646869e-23 6.646869e-23 0.07220401 4.591530
#> hg19_CST7 149.5 4.403301e-21 4.403301e-21 0.22512314 2.640981
#> hg19_NKG7 165.0 8.951222e-21 8.951222e-21 0.51066894 3.815105
#> hg19_GZMH 301.0 1.984392e-19 1.984392e-19 0.00000000 1.972667
#> hg19_GZMB 474.0 3.856340e-17 3.856340e-17 0.11667246 2.017016
#> hg19_CCL5 474.0 1.010639e-16 1.010639e-16 1.04348029 3.772472
#> hg19_FGFBP2 548.0 1.623043e-16 1.623043e-16 0.03101677 1.666924
#> hg19_KLRD1 574.5 4.662465e-16 4.662465e-16 0.09327555 1.568567
#> hg19_EFHD2 794.0 5.121771e-14 5.121771e-14 0.02064028 1.212213
#> hg19_PRF1 801.5 9.024284e-14 9.024284e-14 0.06473009 1.467354
#> meanPct.1 meanPct.2 meanDiff pctDiff name group
#> hg19_GNLY 0.02325581 0.9927007 4.519326 0.9694449 hg19_GNLY control
#> hg19_CST7 0.13953488 0.9927007 2.415857 0.8531658 hg19_CST7 control
#> hg19_NKG7 0.30232558 1.0000000 3.304436 0.6976744 hg19_NKG7 control
#> hg19_GZMH 0.00000000 0.8978102 1.972667 0.8978102 hg19_GZMH control
#> hg19_GZMB 0.06976744 0.8832117 1.900344 0.8134442 hg19_GZMB control
#> hg19_CCL5 0.37209302 1.0000000 2.728992 0.6279070 hg19_CCL5 control
#> hg19_FGFBP2 0.02325581 0.8248175 1.635907 0.8015617 hg19_FGFBP2 control
#> hg19_KLRD1 0.09302326 0.8321168 1.475292 0.7390935 hg19_KLRD1 control
#> hg19_EFHD2 0.02325581 0.7372263 1.191573 0.7139705 hg19_EFHD2 control
#> hg19_PRF1 0.04651163 0.7591241 1.402624 0.7126125 hg19_PRF1 control
#>
#> $ctcl
#> stats.W pval p.adjust meanExprs.1 meanExprs.2
#> hg19_LTB 368.0 6.626368e-28 6.626368e-28 0.1049424 1.978730
#> hg19_RPS26 0.0 4.957273e-23 4.957273e-23 1.6292756 5.072471
#> hg19_IL7R 747.0 5.147332e-21 5.147332e-21 0.1597474 1.651591
#> hg19_SELL 1006.0 3.198651e-20 3.198651e-20 0.0659935 1.152572
#> hg19_LEPROTL1 699.0 1.893136e-18 1.893136e-18 0.2381900 1.300745
#> hg19_EEF1B2 512.5 3.188785e-16 3.188785e-16 1.7119640 3.043623
#> hg19_HBB 1712.5 1.982149e-15 1.982149e-15 0.0000000 0.431026
#> hg19_NOSIP 1034.0 2.135217e-14 2.135217e-14 0.2014222 1.157235
#> hg19_FOS 1278.5 1.229947e-13 1.229947e-13 0.1492607 1.125337
#> hg19_NPM1 927.0 1.013945e-11 1.013945e-11 1.1724979 2.202268
#> meanPct.1 meanPct.2 meanDiff pctDiff name group
#> hg19_LTB 0.08029197 0.9069767 1.8737878 0.8266848 hg19_LTB ctcl
#> hg19_RPS26 0.89051095 1.0000000 3.4431949 0.1094891 hg19_RPS26 ctcl
#> hg19_IL7R 0.10218978 0.8139535 1.4918432 0.7117637 hg19_IL7R ctcl
#> hg19_SELL 0.05109489 0.6976744 1.0865780 0.6465795 hg19_SELL ctcl
#> hg19_LEPROTL1 0.18978102 0.9069767 1.0625555 0.7171957 hg19_LEPROTL1 ctcl
#> hg19_EEF1B2 0.86131387 0.9767442 1.3316593 0.1154303 hg19_EEF1B2 ctcl
#> hg19_HBB 0.00000000 0.4186047 0.4310260 0.4186047 hg19_HBB ctcl
#> hg19_NOSIP 0.19708029 0.7674419 0.9558133 0.5703616 hg19_NOSIP ctcl
#> hg19_FOS 0.11678832 0.6511628 0.9760767 0.5343745 hg19_FOS ctcl
#> hg19_NPM1 0.72992701 0.9534884 1.0297701 0.2235614 hg19_NPM1 ctcl9 Read data from 10X Genomics
Readers unfamiliar with the workflow of converting a count matrix into a SingleCellExperiment object may use the readFrom10X function to convert count matrix from a 10X experiment into an object that can be used for all functions in CiteFuse.
tmpdir <- tempdir()
download.file("http://cf.10xgenomics.com/samples/cell-exp/3.1.0/connect_5k_pbmc_NGSC3_ch1/connect_5k_pbmc_NGSC3_ch1_filtered_feature_bc_matrix.tar.gz", file.path(tmpdir, "/5k_pbmc_NGSC3_ch1_filtered_feature_bc_matrix.tar.gz"))
untar(file.path(tmpdir, "5k_pbmc_NGSC3_ch1_filtered_feature_bc_matrix.tar.gz"),
exdir = tmpdir)
sce_citeseq_10X <- readFrom10X(file.path(tmpdir, "filtered_feature_bc_matrix/"))
sce_citeseq_10X10 SessionInfo
sessionInfo()
#> R version 4.1.1 (2021-08-10)
#> Platform: x86_64-pc-linux-gnu (64-bit)
#> Running under: Ubuntu 20.04.3 LTS
#>
#> Matrix products: default
#> BLAS: /home/biocbuild/bbs-3.14-bioc/R/lib/libRblas.so
#> LAPACK: /home/biocbuild/bbs-3.14-bioc/R/lib/libRlapack.so
#>
#> locale:
#> [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
#> [3] LC_TIME=en_GB LC_COLLATE=C
#> [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] stats4 stats graphics grDevices utils datasets methods
#> [8] base
#>
#> other attached packages:
#> [1] mclust_5.4.7 gridExtra_2.3
#> [3] DT_0.19 scater_1.22.0
#> [5] ggplot2_3.3.5 scuttle_1.4.0
#> [7] SingleCellExperiment_1.16.0 SummarizedExperiment_1.24.0
#> [9] Biobase_2.54.0 GenomicRanges_1.46.0
#> [11] GenomeInfoDb_1.30.0 IRanges_2.28.0
#> [13] S4Vectors_0.32.0 BiocGenerics_0.40.0
#> [15] MatrixGenerics_1.6.0 matrixStats_0.61.0
#> [17] CiteFuse_1.6.0 BiocStyle_2.22.0
#>
#> loaded via a namespace (and not attached):
#> [1] ggbeeswarm_0.6.0 Rtsne_0.15
#> [3] colorspace_2.0-2 ellipsis_0.3.2
#> [5] ggridges_0.5.3 bluster_1.4.0
#> [7] XVector_0.34.0 BiocNeighbors_1.12.0
#> [9] farver_2.1.0 graphlayouts_0.7.1
#> [11] ggrepel_0.9.1 RSpectra_0.16-0
#> [13] fansi_0.5.0 splines_4.1.1
#> [15] sparseMatrixStats_1.6.0 knitr_1.36
#> [17] polyclip_1.10-0 jsonlite_1.7.2
#> [19] cluster_2.1.2 kernlab_0.9-29
#> [21] uwot_0.1.10 pheatmap_1.0.12
#> [23] ggforce_0.3.3 BiocManager_1.30.16
#> [25] compiler_4.1.1 dqrng_0.3.0
#> [27] assertthat_0.2.1 Matrix_1.3-4
#> [29] fastmap_1.1.0 limma_3.50.0
#> [31] tweenr_1.0.2 BiocSingular_1.10.0
#> [33] htmltools_0.5.2 tools_4.1.1
#> [35] rsvd_1.0.5 igraph_1.2.7
#> [37] gtable_0.3.0 glue_1.4.2
#> [39] GenomeInfoDbData_1.2.7 reshape2_1.4.4
#> [41] dplyr_1.0.7 Rcpp_1.0.7
#> [43] jquerylib_0.1.4 vctrs_0.3.8
#> [45] rhdf5filters_1.6.0 crosstalk_1.1.1
#> [47] DelayedMatrixStats_1.16.0 ggraph_2.0.5
#> [49] xfun_0.27 stringr_1.4.0
#> [51] beachmat_2.10.0 lifecycle_1.0.1
#> [53] irlba_2.3.3 statmod_1.4.36
#> [55] edgeR_3.36.0 zlibbioc_1.40.0
#> [57] MASS_7.3-54 scales_1.1.1
#> [59] tidygraph_1.2.0 parallel_4.1.1
#> [61] rhdf5_2.38.0 RColorBrewer_1.1-2
#> [63] yaml_2.2.1 sass_0.4.0
#> [65] segmented_1.3-4 stringi_1.7.5
#> [67] highr_0.9 ScaledMatrix_1.2.0
#> [69] randomForest_4.6-14 scran_1.22.0
#> [71] BiocParallel_1.28.0 rlang_0.4.12
#> [73] pkgconfig_2.0.3 bitops_1.0-7
#> [75] evaluate_0.14 lattice_0.20-45
#> [77] purrr_0.3.4 Rhdf5lib_1.16.0
#> [79] labeling_0.4.2 htmlwidgets_1.5.4
#> [81] cowplot_1.1.1 tidyselect_1.1.1
#> [83] plyr_1.8.6 magrittr_2.0.1
#> [85] bookdown_0.24 R6_2.5.1
#> [87] magick_2.7.3 generics_0.1.1
#> [89] metapod_1.2.0 DelayedArray_0.20.0
#> [91] DBI_1.1.1 withr_2.4.2
#> [93] pillar_1.6.4 mixtools_1.2.0
#> [95] survival_3.2-13 RCurl_1.98-1.5
#> [97] tibble_3.1.5 crayon_1.4.1
#> [99] utf8_1.2.2 rmarkdown_2.11
#> [101] viridis_0.6.2 locfit_1.5-9.4
#> [103] grid_4.1.1 FNN_1.1.3
#> [105] propr_4.2.6 digest_0.6.28
#> [107] tidyr_1.1.4 dbscan_1.1-8
#> [109] munsell_0.5.0 beeswarm_0.4.0
#> [111] viridisLite_0.4.0 vipor_0.4.5
#> [113] bslib_0.3.1