sc-RAN-seq 數據分析||Seurat新版教程：整合分析
- 2020 年 3 月 30 日
- 筆記
如果只是做單個樣本的sc-RNA-seq數據分析，並不能體會到Seurat的強大，因為Seurat天生為整合而生。
本教程展示的是兩個pbmc數據（受刺激組和對照組）整合分析策略，執行整合分析，以便識別常見細胞類型以及比較分析。雖然本例只展示了兩個數據集，但是本方法已經能夠處理多個數據集了。
整個分析的目的：
- 識別兩個數據集中都存在的細胞類型
- 在對照組和受刺激組均存在的細胞類型標記（cell type markers）
- 比較數據集，找出對刺激有反應的特殊細胞類型（cell-type）
數據準備
我已經下載好數據了，但是： 遇到的第一個問題就是，數據太大在windows上Rstudio連數據都讀不了。誰叫我是伺服器的男人呢，Windows讀不了沒關係啊，我到伺服器上操作，生成rds在讀到Rstudio裡面。然後就遇到
scRNAseq.integrated <- RunUMAP(object = scRNAseq.integrated, reduction = "pca", dims = 1:30) Error in RunUMAP.default(object = data.use, assay = assay, n.neighbors = n.neighbors, : Cannot find UMAP, please install through pip (e.g. pip install umap-learn).
我明明已經裝了umap-learn了呀，而且本地跑RunUMAP沒問題，投遞上去就不行。Google了半天，原來是conda的Python與R之間的調度不行，於是
library(reticulate) use_python("pathto/personal_dir/zhouyunlai/software/conda/envs/scRNA/bin/python")
可以了。
library(Seurat) library(cowplot) ctrl.data <- read.table(file = "../data/immune_control_expression_matrix.txt.gz", sep = "t") stim.data <- read.table(file = "../data/immune_stimulated_expression_matrix.txt.gz", sep = "t") # Set up control object ctrl <- CreateSeuratObject(counts = ctrl.data, project = "IMMUNE_CTRL", min.cells = 5) ctrl$stim <- "CTRL" ctrl <- subset(ctrl, subset = nFeature_RNA > 500) ctrl <- NormalizeData(ctrl, verbose = FALSE) ctrl <- FindVariableFeatures(ctrl, selection.method = "vst", nfeatures = 2000) # Set up stimulated object stim <- CreateSeuratObject(counts = stim.data, project = "IMMUNE_STIM", min.cells = 5) stim$stim <- "STIM" stim <- subset(stim, subset = nFeature_RNA > 500) stim <- NormalizeData(stim, verbose = FALSE) stim <- FindVariableFeatures(stim, selection.method = "vst", nfeatures = 2000)
在針對SeuratV3 的文章Comprehensive integration of single cell data中Anchors 是十分核心的概念。翻譯成漢語叫做錨也就是基於CCA的一種數據比對（alignment）的方法。所以這兩個函數亦需要看一下，以這樣的方式來找到兩個以致多個數據集的共有結構，這不是代替了之前的函數RunCCA()的應用場景了嗎？
##Perform integration ?FindIntegrationAnchors ?IntegrateData immune.anchors <- FindIntegrationAnchors(object.list = list(ctrl, stim), dims = 1:20) immune.combined <- IntegrateData(anchorset = immune.anchors, dims = 1:20)
整合完之後，下面的操作就比較熟悉了，和單樣本的思路一樣。
#Perform an integrated analysis DefaultAssay(immune.combined) <- "integrated" # Run the standard workflow for visualization and clustering immune.combined <- ScaleData(immune.combined, verbose = FALSE) immune.combined <- RunPCA(immune.combined, npcs = 30, verbose = FALSE) # t-SNE and Clustering immune.combined <- RunUMAP(immune.combined, reduction = "pca", dims = 1:20) immune.combined <- FindNeighbors(immune.combined, reduction = "pca", dims = 1:20) immune.combined <- FindClusters(immune.combined, resolution = 0.5)
以上，都是我在服務上跑的，所以我要把他們讀進來：
immune.combined<-readRDS("D:\Users\Administrator\Desktop\RStudio\single_cell\seurat_files_nbt\seurat_files_nbt\immune.combined_tutorial.rds") > immune.combined An object of class Seurat 16053 features across 13999 samples within 2 assays Active assay: integrated (2000 features) 1 other assay present: RNA 2 dimensional reductions calculated: pca, umap
# Visualization p1 <- DimPlot(immune.combined, reduction = "umap", group.by = "stim") p2 <- DimPlot(immune.combined, reduction = "umap", label = TRUE) plot_grid(p1, p2)
可以用split.by 參數來分別展示兩個數據：
DimPlot(immune.combined, reduction = "umap", split.by = "stim")
Identify conserved cell type markers
所謂保守的和高變的是對應的，也可以理解為兩個數據集中一致的markers.FindConservedMarkers()函數對兩個數據集執行差異檢驗，並使用MetaDE R包中的meta分析方法組合p值。例如，我們可以計算出在cluster 6 (NK細胞)中，無論刺激條件如何，都是保守標記的基因。但凡遇到差異分析的部分都會比較耗時。
#Identify conserved cell type markers ? FindConservedMarkers DefaultAssay(immune.combined) <- "RNA" nk.markers <- FindConservedMarkers(immune.combined, ident.1 = 7, grouping.var = "stim", verbose = FALSE) head(nk.markers) CTRL_p_val CTRL_avg_logFC CTRL_pct.1 CTRL_pct.2 CTRL_p_val_adj STIM_p_val STIM_avg_logFC STIM_pct.1 STIM_pct.2 STIM_p_val_adj max_pval minimump_p_val GNLY 0 4.186117 0.943 0.046 0 0.000000e+00 4.033650 0.955 0.061 0.000000e+00 0.000000e+00 0 NKG7 0 3.164712 0.953 0.085 0 0.000000e+00 2.914724 0.952 0.082 0.000000e+00 0.000000e+00 0 GZMB 0 2.915692 0.839 0.044 0 0.000000e+00 3.142391 0.898 0.061 0.000000e+00 0.000000e+00 0 CLIC3 0 2.407695 0.601 0.024 0 0.000000e+00 2.470769 0.629 0.031 0.000000e+00 0.000000e+00 0 FGFBP2 0 2.241968 0.500 0.021 0 9.524349e-156 1.483922 0.259 0.016 1.338457e-151 9.524349e-156 0 CTSW 0 2.088278 0.537 0.030 0 0.000000e+00 2.196390 0.604 0.035 0.000000e+00 0.000000e+00 0
FeaturePlot(immune.combined, features = c("CD3D", "SELL", "CREM", "CD8A", "GNLY", "CD79A", "FCGR3A", "CCL2", "PPBP"), min.cutoff = "q9")
immune.combined <- RenameIdents(immune.combined, `0` = "CD14 Mono", `1` = "CD4 Naive T", `2` = "CD4 Memory T", `3` = "CD16 Mono", `4` = "B", `5` = "CD8 T", `6` = "T activated", `7` = "NK", `8` = "DC", `9` = "B Activated", `10` = "Mk", `11` = "pDC", `12` = "Eryth", `13` = "Mono/Mk Doublets") DimPlot(immune.combined, label = TRUE)
Idents(immune.combined) <- factor(Idents(immune.combined), levels = c("Mono/Mk Doublets", "pDC", "Eryth", "Mk", "DC", "CD14 Mono", "CD16 Mono", "B Activated", "B", "CD8 T", "NK", "T activated", "CD4 Naive T", "CD4 Memory T")) markers.to.plot <- c("CD3D", "CREM", "HSPH1", "SELL", "GIMAP5", "CACYBP", "GNLY", "NKG7", "CCL5", "CD8A", "MS4A1", "CD79A", "MIR155HG", "NME1", "FCGR3A", "VMO1", "CCL2", "S100A9", "HLA-DQA1", "GPR183", "PPBP", "GNG11", "HBA2", "HBB", "TSPAN13", "IL3RA", "IGJ") DotPlot(immune.combined, features = rev(markers.to.plot), cols = c("blue", "red"), dot.scale = 8, split.by = "stim") + RotatedAxis()
差異基因
在這裡，我們取受刺激和受控制的原始T細胞和CD14單核細胞群的平均表達量，並生成散點圖，突出顯示對干擾素刺激有顯著反應的基因。
#Identify differential expressed genes across conditions t.cells <- subset(immune.combined, idents = "CD4 Naive T") Idents(t.cells) <- "stim" avg.t.cells <- log1p(AverageExpression(t.cells, verbose = FALSE)$RNA) avg.t.cells$gene <- rownames(avg.t.cells) cd14.mono <- subset(immune.combined, idents = "CD14 Mono") Idents(cd14.mono) <- "stim" avg.cd14.mono <- log1p(AverageExpression(cd14.mono, verbose = FALSE)$RNA) avg.cd14.mono$gene <- rownames(avg.cd14.mono) genes.to.label = c("ISG15", "LY6E", "IFI6", "ISG20", "MX1", "IFIT2", "IFIT1", "CXCL10", "CCL8") p1 <- ggplot(avg.t.cells, aes(CTRL, STIM)) + geom_point() + ggtitle("CD4 Naive T Cells") p1 <- LabelPoints(plot = p1, points = genes.to.label, repel = TRUE) p2 <- ggplot(avg.cd14.mono, aes(CTRL, STIM)) + geom_point() + ggtitle("CD14 Monocytes") p2 <- LabelPoints(plot = p2, points = genes.to.label, repel = TRUE) plot_grid(p1, p2)
我們來用FindMarkers()看看這些基因是不是marker基因。
immune.combined$celltype.stim <- paste(Idents(immune.combined), immune.combined$stim, sep = "_") immune.combined$celltype <- Idents(immune.combined) Idents(immune.combined) <- "celltype.stim" b.interferon.response <- FindMarkers(immune.combined, ident.1 = "B_STIM", ident.2 = "B_CTRL", verbose = FALSE) head(b.interferon.response, n = 15) p_val avg_logFC pct.1 pct.2 p_val_adj ISG15 8.611499e-155 3.1934171 0.998 0.236 1.210174e-150 IFIT3 1.319470e-150 3.1195144 0.965 0.053 1.854251e-146 IFI6 4.716672e-148 2.9264004 0.964 0.078 6.628339e-144 ISG20 1.061563e-145 2.0390802 1.000 0.664 1.491814e-141 IFIT1 1.830963e-136 2.8706318 0.909 0.030 2.573053e-132 MX1 1.775606e-120 2.2540787 0.909 0.118 2.495259e-116 LY6E 2.824749e-116 2.1460522 0.896 0.153 3.969620e-112 TNFSF10 4.227184e-109 2.6372382 0.785 0.020 5.940461e-105 IFIT2 4.627440e-106 2.5102230 0.789 0.038 6.502941e-102 B2M 1.344345e-94 0.4193618 1.000 1.000 1.889208e-90 PLSCR1 5.170871e-94 1.9769476 0.794 0.113 7.266624e-90 IRF7 1.451494e-92 1.7994058 0.838 0.190 2.039785e-88 CXCL10 6.201621e-84 3.6906104 0.650 0.010 8.715138e-80 UBE2L6 1.324818e-81 1.4879509 0.854 0.301 1.861767e-77 PSMB9 1.098134e-76 1.1378896 0.940 0.571 1.543208e-72
這裡構造數據的過程值得玩味，然後繪製兩樣本的小提琴圖，那麼問題來了：兩個以上數據集的小提琴圖要如何繪製呢？
FeaturePlot(immune.combined, features = c("CD3D", "GNLY", "IFI6"), split.by = "stim", max.cutoff = 3, cols = c("grey", "red"))
plots <- VlnPlot(immune.combined, features = c("LYZ", "ISG15", "CXCL10"), split.by = "stim", group.by = "celltype", pt.size = 0, combine = FALSE) CombinePlots(plots = plots, ncol = 1)
