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前边咱们演示了10X空转的上游分析（10X-Visum空间转录组(1)---上游分析），主如果为了叮咛一些罕见的景色，从这节运转，咱们将逐步进行卑劣分析。其实卑劣分析仍是不是什么难事了，岂论是官网，如故其他阶梯，皆有很注主义演示不错参考，咱们不错对比一下，搞显然其中的一些细节。本节本色已发布微信VIP。

咱们这里演示的是多个样本，如果您是单个的，大略需要单独分析，那么径直走单个的经过即可，无谓合并分析。分析如故使用熟练的seurat，熟练的配方！

setwd("/home/tq_ziv/data_analysis/10X空间转录组/")library(Seurat)library(ggplot2)library(hdf5r)library(tidydr)

加载数据，load data原本并不是什么需要说的，然而毕竟跟着各人数据库的增多，好多本领需要讹诈别东谈主的数据，那么这本领读取数据可能就不是那么顺畅了。就像scRNA教程开首相同，咱们写了好多种情况的数据读取。空间转录组亦然如斯，如果我方跑了space ranger上游，获得了数据，那么就很好读取了，Load10X_Spatial即可。读取条目是将抒发矩阵filtered_feature_bc_matrix.h5文献和spatial文献夹放在合并目次下。咱们有多个data，分离读取！

#Early1Early1 <- CreateSeuratObject(counts = Read10X("./raw/Early_R1/"), assay = "Spatial")#读取exp matrix，并创建seurat objEarly1_img <- Read10X_Image(image.dir = file.path("./sptial/Early_R01_S1_spatial/"), filter.matrix = TRUE)#Load a 10X Genomics Visium ImageEarly1_img <- Early1_img[Cells(x = Early1)]DefaultAssay(Early1 = Early1_img) <- "Spatial"Early1[["slice1"]] <- Early1_img#Early2Early2 <- CreateSeuratObject(counts = Read10X("./raw/Early_R2/"), assay = "Spatial")#读取exp matrix，并创建seurat objEarly2_img <- Read10X_Image(image.dir = file.path("./sptial/Early_R02_S1_spatial/"), filter.matrix = TRUE)#Load a 10X Genomics Visium ImageEarly2_img <- Early2_img[Cells(x = Early2)]DefaultAssay(Early2 = Early2_img) <- "Spatial"Early2[["slice1"]] <- Early2_img#Mid1Mid1 <- CreateSeuratObject(counts = Read10X("./raw/Mid_R1/"), assay = "Spatial")#读取exp matrix，并创建seurat objMid1_img <- Read10X_Image(image.dir = file.path("./sptial/Mid_R01_S1_spatial/"), filter.matrix = TRUE)#Load a 10X Genomics Visium ImageMid1_img <- Mid1_img[Cells(x = Mid1)]DefaultAssay(Mid1 = Mid1_img) <- "Spatial"Mid1[["slice1"]] <- Mid1_img#Mid2Mid2 <- CreateSeuratObject(counts = Read10X("./raw/Mid_R2/"), assay = "Spatial")#读取exp matrix，并创建seurat objMid2_img <- Read10X_Image(image.dir = file.path("./sptial/Mid_R02_S2_spatial/"), filter.matrix = TRUE)#Load a 10X Genomics Visium ImageMid2_img <- Mid2_img[Cells(x = Mid2)]DefaultAssay(Mid2 = Mid2_img) <- "Spatial"Mid2[["slice1"]] <- Mid2_img#Old1Old1 <- CreateSeuratObject(counts = Read10X("./raw/Old_R1/"), assay = "Spatial")#读取exp matrix，并创建seurat objOld1_img <- Read10X_Image(image.dir = file.path("./sptial/Old_R01_S1_spatial/"), filter.matrix = TRUE)#Load a 10X Genomics Visium ImageOld1_img <- Old1_img[Cells(x = Old1)]DefaultAssay(Old1 = Old1_img) <- "Spatial"Old1[["slice1"]] <- Old1_img#Old2Old2 <- CreateSeuratObject(counts = Read10X("./raw/Old_R2/"), assay = "Spatial")#读取exp matrix，并创建seurat objOld2_img <- Read10X_Image(image.dir = file.path("./sptial/Old_R02_S2_spatial/"), filter.matrix = TRUE)#Load a 10X Genomics Visium ImageOld2_img <- Old2_img[Cells(x = Old2)]DefaultAssay(Old2 = Old2_img) <- "Spatial"Old2[["slice1"]] <- Old2_img

质控，QC无非等于对每个spot的features、counts、大略线粒体基因的比例的质控。因为spots并不是像单个细胞，我对比了好多的著作，他们质控并不是一致的,可能需要具体对待，有的著作致使莫得进行质控!

Spatial_list <- list(Early1,Early2,Mid1,Mid2,Old1,Old2)names(Spatial_list) <- c("Early1","Early2","Mid1","Mid2","Old1","Old2")Spatial_merge <-  Reduce(function(x,y) merge(x,y) , Spatial_list) Spatial_merge <- Spatial_merge[,Spatial_merge$nCount_Spatial >=5]

多个数据整合分析：

DefaultAssay(Spatial_merge) <- 'Spatial'object_splitlist <- SplitObject(Spatial_merge, split.by = "orig.ident")for (i in names(object_splitlist)) {  object_splitlist[[i]] <- SCTransform(object_splitlist[[i]], verbose = T, assay = 'Spatial')}#这就和作念scRNA的没啥区别了，nfeatures不错自行遴荐调度Integration.features <- SelectIntegrationFeatures(object.list = object_splitlist, nfeatures = 2000)object_splitlist <- PrepSCTIntegration(object.list = object_splitlist, anchor.features = Integration.features, verbose = T)#integration，因为是cca整合，速率可能会稍稍慢少许，耐性恭候integration.anchors <- FindIntegrationAnchors(object.list = object_splitlist, normalization.method = "SCT",                                              anchor.features = Integration.features, verbose = T)Spatial_integrated <- IntegrateData(anchorset =integration.anchors, normalization.method = "SCT")

降维聚类：

Spatial_integrated <- RunPCA(object = Spatial_integrated, verbose = T)Spatial_integrated <- FindNeighbors(Spatial_integrated, dims = 1:30)Spatial_integrated <- FindClusters(Spatial_integrated, resolution = 0.8)#resolution可成就多个，自行遴荐Spatial_integrated <- RunUMAP(Spatial_integrated, dims = 1:30, verbose = T)

可视化聚类，和scRNA相同，望望spots分群：

cols= c("#EDB931","#eb6841","#cc2a36","#00a0b0","#7A989A", "#849271", "#CF9546", "#C67052", "#C1AE8D",        "#3F6F76", "#C65840", "#62496F", "#69B7CE","#91323A", "#3A4960", "#6D7345", "#D7C969",        "#C1395E", "#AEC17B", "#E07B42", "#89A7C2", "#F0CA50","#a53e1f", "#457277", "#8f657d", "#8dcee2",        "#E69253", "#EDB931", "#E4502E", "#4378A0", "#272A2A","#3F6148", "#A4804C", "#4B5F80", "#DBD3A4")#转录组UMAP降维效果DimPlot(Spatial_integrated, label = F, cols = cols,pt.size = 0.1)+  theme_dr()+theme(panel.grid.major = element_blank(),                   panel.grid.minor = element_blank())

图片

展示spots空间位置！

patialDimPlot(Spatial_integrated, stroke=0.1,ncol=3)&   scale_fill_manual(values = cols) &  theme_bw()&  theme(axis.text = element_blank(),        axis.ticks = element_blank(),        axis.title = element_blank())

图片

熟练了scRNA的经过，那么空转的分析也会很顺畅，到这里关于空转，才算是运转。那么有一个问题等于，既然空转不是单细胞，每个spot其实包含几个细胞，那么接下来的要点等于如何进行谛视了，也等于常传说的反卷积，咱们后头迟缓了解。那么咱们如故但愿空转能尽快冲破单细胞水平吧！但愿咱们的共享对你灵验，单个赞再走呗!