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单细胞转录组基础分析五：细胞再聚类
发布日期：2021-07-16浏览：
次
单细胞数据分析中，一般需要对可以细分的细胞再聚类，比如本次分析中的T细胞群体可以细分为Naive T cells、CD8+ T cells、Treg cells、Tmemory cells等。细胞子集的提取使用subset函数，主要依据meta.data的分类项目选择，也可以自定义细胞barcode提取。
提取细胞子集
重新降维聚类
因为再聚类的细胞之间差异比较小，所以聚类函数FindClusters()控制分辨率的参数建议调高到resolution = 0.9。
Cluster差异分析
SingleR细胞鉴定
Subcluster的细胞同样可以使用SingleR鉴定细胞类型。使用的时候注意调整参考数据库和分类标签，以便鉴定结果更有针对性。上节使用SingleR时使用的参考数据库是人类主要细胞图谱（HumanPrimaryCellAtlasData），采用分类标签是主分类标签（label.main）；这次建议使用人类免疫细胞数据（MonacoImmuneData），分类标签采用精细分类标签（label.fine）。希望详细了解SingleR的朋友可以到github看看：
https://github.com/dviraran/singler
library(Seurat)library(monocle)library(tidyverse)library(patchwork)rm(list=ls())dir.create("subcluster")scRNA <- readRDS("scRNA.rds")##提取细胞子集Cells.sub <- subset(scRNA@meta.data, celltype=="T_cells")scRNAsub <- subset(scRNA, cells=row.names(Cells.sub))
##PCA降维scRNAsub <- FindVariableFeatures(scRNAsub, selection.method = "vst", nfeatures = 2000)scale.genes <- rownames(scRNAsub)scRNAsub <- ScaleData(scRNAsub, features = scale.genes)scRNAsub <- RunPCA(scRNAsub, features = VariableFeatures(scRNAsub))ElbowPlot(scRNAsub, ndims=20, reduction="pca")pc.num=1:10##细胞聚类scRNAsub <- FindNeighbors(scRNAsub, dims = pc.num) scRNAsub <- FindClusters(scRNAsub, resolution = 0.9)table(scRNAsub@meta.data$seurat_clusters)metadata <- scRNAsub@meta.datacell_cluster <- data.frame(cell_ID=rownames(metadata), cluster_ID=metadata$seurat_clusters)write.csv(cell_cluster,'subcluster/cell_cluster.csv',row.names = F)##非线性降维#tSNEscRNAsub = RunTSNE(scRNAsub, dims = pc.num)embed_tsne <- Embeddings(scRNAsub, 'tsne')write.csv(embed_tsne,'subcluster/embed_tsne.csv')plot1 = DimPlot(scRNAsub, reduction = "tsne") ggsave("subcluster/tSNE.pdf", plot = plot1, width = 8, height = 7)ggsave("subcluster/tSNE.png", plot = plot1, width = 8, height = 7)#UMAPscRNAsub <- RunUMAP(scRNAsub, dims = pc.num)embed_umap <- Embeddings(scRNAsub, 'umap')write.csv(embed_umap,'subcluster/embed_umap.csv') plot2 = DimPlot(scRNAsub, reduction = "umap") ggsave("subcluster/UMAP.pdf", plot = plot2, width = 8, height = 7)ggsave("subcluster/UMAP.png", plot = plot2, width = 8, height = 7)#合并tSNE与UMAPplotc <- plot1+plot2+ plot_layout(guides = 'collect')ggsave("subcluster/tSNE_UMAP.pdf", plot = plotc, width = 10, height = 5)ggsave("subcluster/tSNE_UMAP.png", plot = plotc, width = 10, height = 5)
diff.wilcox = FindAllMarkers(scRNAsub)all.markers = diff.wilcox %>% select(gene, everything()) %>% subset(p_val<0.05)top10 = all.markers %>% group_by(cluster) %>% top_n(n = 10, wt = avg_logFC)write.csv(all.markers, "subcluster/diff_genes_wilcox.csv", row.names = F)write.csv(top10, "subcluster/top10_diff_genes_wilcox.csv", row.names = F)
##细胞类型鉴定library(SingleR)refdata <- MonacoImmuneData()testdata <- GetAssayData(scRNAsub, slot="data")clusters <- scRNAsub@meta.data$seurat_clusterscellpred <- SingleR(test = testdata, ref = refdata, labels = refdata$label.fine, method = "cluster", clusters = clusters, assay.type.test = "logcounts", assay.type.ref = "logcounts")celltype = data.frame(ClusterID=rownames(cellpred), celltype=cellpred$labels, stringsAsFactors = F)write.csv(celltype,"subcluster/celltype_singleR.csv",row.names = F)scRNAsub@meta.data$celltype = "NA"for(i in 1:nrow(celltype)){scRNAsub@meta.data[which(scRNAsub@meta.data$seurat_clusters == celltype$ClusterID[i]),'celltype'] <- celltype$celltype[i]}p1 = DimPlot(scRNAsub, group.by="celltype", label=T, label.size=5, reduction='tsne')p2 = DimPlot(scRNAsub, group.by="celltype", label=T, label.size=5, reduction='umap')p3 = plotc <- p1+p2+ plot_layout(guides = 'collect')ggsave("subcluster/tSNE_celltype.pdf", p1, width=7 ,height=6)ggsave("subcluster/UMAP_celltype.pdf", p2, width=7 ,height=6)ggsave("subcluster/celltype.pdf", p3, width=10 ,height=5)ggsave("subcluster/celltype.png", p3, width=10 ,height=5)
