标准的Seurat工作流程
标准的Seurat工作流程采用原始的单细胞表达数据，并旨在在数据中查找簇。有关完整的详细信息，请阅读我们的教程。此过程包括数据标准化和可变特征选择，数据缩放，可变特征上的PCA，共享最近邻图的构建以及使用模块化优化器的聚类。最后，我们使用t-SNE在二维空间中可视化群集。
pbmc.counts <- Read10X(data.dir = "~/Downloads/pbmc3k/filtered_gene_bc_matrices/hg19/")
pbmc <- CreateSeuratObject(counts = pbmc.counts)
pbmc <- NormalizeData(object = pbmc)
pbmc <- FindVariableFeatures(object = pbmc)
pbmc <- ScaleData(object = pbmc)
pbmc <- RunPCA(object = pbmc)
pbmc <- FindNeighbors(object = pbmc)
pbmc <- FindClusters(object = pbmc)
pbmc <- RunTSNE(object = pbmc)
DimPlot(object = pbmc, reduction = "tsne")
对象互动
使用Seurat v3.0，我们对Seurat对象进行了改进，并增加了用于用户交互的新方法。我们还为镜像R的普通任务引入了简单的函数，例如子集和合并。
# Get cell and feature names, and total numbers
colnames(x = pbmc)
Cells(object = pbmc)
rownames(x = pbmc)
ncol(x = pbmc)
nrow(x = pbmc)
# Get cell identity classes
Idents(object = pbmc)
levels(x = pbmc)
# Stash cell identity classes
pbmc[["old.ident"]] <- Idents(object = pbmc)
pbmc <- StashIdent(object = pbmc, save.name = "old.ident")
# Set identity classes
Idents(object = pbmc) <- "CD4 T cells"
Idents(object = pbmc, cells = 1:10) <- "CD4 T cells"
# Set identity classes to an existing column in meta data
Idents(object = pbmc, cells = 1:10) <- "orig.ident"
Idents(object = pbmc) <- "orig.ident"
# Rename identity classes
pbmc <- RenameIdents(object = pbmc, `CD4 T cells` = "T Helper cells")
# Subset Seurat object based on identity class, also see ?SubsetData
subset(x = pbmc, idents = "B cells")
subset(x = pbmc, idents = c("CD4 T cells", "CD8 T cells"), invert = TRUE)
# Subset on the expression level of a gene/feature
subset(x = pbmc, subset = MS4A1 > 3)
# Subset on a combination of criteria
subset(x = pbmc, subset = MS4A1 > 3 & PC1 > 5)
subset(x = pbmc, subset = MS4A1 > 3, idents = "B cells")
# Subset on a value in the object meta data
subset(x = pbmc, subset = orig.ident == "Replicate1")
# Downsample the number of cells per identity class
subset(x = pbmc, downsample = 100)
# Merge two Seurat objects
merge(x = pbmc1, y = pbmc2)
# Merge more than two Seurat objects
merge(x = pbmc1, y = list(pbmc2, pbmc3))
访问数据
在Seurat中访问数据非常简单，使用明确定义的访问器和设置器即可快速找到所需的数据。
# View metadata data frame, stored in [email protected]
pbmc[[]]
# Retrieve specific values from the metadata
pbmc$nCount_RNA
pbmc[[c("percent.mito", "nFeature_RNA")]]
# Add metadata, see ?AddMetaData
random_group_labels <- sample(x = c("g1", "g2"), size = ncol(x = pbmc), replace = TRUE)
pbmc$groups <- random_group_labels
# Retrieve or set data in an expression matrix ('counts', 'data', and 'scale.data')
GetAssayData(object = pbmc, slot = "counts")
pbmc <- SetAssayData(object = pbmc, slot = "scale.data", new.data = new.data)
# Get cell embeddings and feature loadings
Embeddings(object = pbmc, reduction = "pca")
Loadings(object = pbmc, reduction = "pca")
Loadings(object = pbmc, reduction = "pca", projected = TRUE)
# FetchData can pull anything from expression matrices, cell embeddings, or metadata
FetchData(object = pbmc, vars = c("PC_1", "percent.mito", "MS4A1"))
数据可视化
Seurat有一个庞大的基于ggplot2的绘图库。默认情况下，所有绘图功能都将返回ggplot2绘图，从而允许使用ggplot2轻松自定义。
# Dimensional reduction plot for PCA or tSNE
DimPlot(object = pbmc, reduction = "tsne")
DimPlot(object = pbmc, reduction = "pca")
# Dimensional reduction plot, with cells colored by a quantitative feature
FeaturePlot(object = pbmc, features = "MS4A1")
# Scatter plot across single cells, replaces GenePlot
FeatureScatter(object = pbmc, feature1 = "MS4A1", feature2 = "PC_1")
FeatureScatter(object = pbmc, feature1 = "MS4A1", feature2 = "CD3D")
# Scatter plot across individual features, repleaces CellPlot
CellScatter(object = pbmc, cell1 = "AGTCTACTAGGGTG", cell2 = "CACAGATGGTTTCT")
VariableFeaturePlot(object = pbmc)
# Violin and Ridge plots
VlnPlot(object = pbmc, features = c("LYZ", "CCL5", "IL32"))
RidgePlot(object = pbmc, feature = c("LYZ", "CCL5", "IL32"))
# Heatmaps
DoHeatmap(object = pbmc, features = heatmap_markers)
DimHeatmap(object = pbmc, reduction = "pca", cells = 200)
# New things to try! Note that plotting functions now return ggplot2 objects, so you can add themes, titles, and options
# onto them
VlnPlot(object = pbmc, features = "MS4A1", split.by = "groups")
DotPlot(object = pbmc, features = c("LYZ", "CCL5", "IL32"), split.by = "groups")
FeaturePlot(object = pbmc, features = c("MS4A1", "CD79A"), blend = TRUE)
DimPlot(object = pbmc) + DarkTheme()
DimPlot(object = pbmc) + labs(title = "2,700 PBMCs clustered using Seurat and viewed\non a two-dimensional tSNE")
Seurat提供了许多预建主题，可以将其添加到ggplot2图中以进行快速自定义
主题 功能
DarkTheme 设置带有白色文本的黑色背景
FontSize 设置图的各种元素的字体大小
NoAxes 删除轴和轴文本
NoLegend 删除所有图例元素
RestoreLegend 删除后恢复图例
RotatedAxis 旋转x轴标签
# Plotting helper functions work with ggplot2-based scatter plots, such as DimPlot, FeaturePlot, CellScatter, and
# FeatureScatter
plot <- DimPlot(object = pbmc) + NoLegend()
# HoverLocator replaces the former `do.hover` argument It can also show extra data throught the `information` argument,
# designed to work smoothly with FetchData
HoverLocator(plot = plot, information = FetchData(object = pbmc, vars = c("ident", "PC_1", "nFeature_RNA")))
# FeatureLocator replaces the former `do.identify`
select.cells <- FeatureLocator(plot = plot)
# Label points on a ggplot object
LabelPoints(plot = plot, points = TopCells(object = pbmc[["pca"]]), repel = TRUE)
多重分析功能
使用Seurat v3.0，您可以轻松地在单个细胞水平上在不同的测定之间切换（例如，来自CITE-seq的ADT计数或经过积分/批校正的数据）。现在，大多数功能都带有化验参数，但是您可以将默认化验设置为不重复的语句。
cbmc <- CreateSeuratObject(counts = cbmc.rna)
# Add ADT data
cbmc[["ADT"]] <- CreateAssayObject(counts = cbmc.adt)
# Run analyses by specifying the assay to use
NormalizeData(object = cbmc, assay = "RNA")
NormalizeData(object = cbmc, assay = "ADT", method = "CLR")
# Retrieve and set the default assay
DefaultAssay(object = cbmc)
DefaultAssay(object = cbmc) <- "ADT"
DefaultAssay(object = cbmc)
# Pull feature expression from both assays by using keys
FetchData(object = cbmc, vars = c("rna_CD3E", "adt_CD3"))
# Plot data from multiple assays using keys
FeatureScatter(object = cbmc, feature1 = "rna_CD3E", feature2 = "adt_CD3")
V2 V3 区别
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https://satijalab.org/seurat/essential_commands.html