单细胞多样本多平台合并分析（二）

继续上篇文章所做的，接下来进行数据质控使用R语言代码：

scRNA <- scRNA3  #以后的分析使用整合的数据进行
##meta.data添加信息
proj_name <- data.frame(proj_name=rep("demo2",ncol(scRNA)))
rownames(proj_name) <- row.names(scRNA@meta.data)
scRNA <- AddMetaData(scRNA, proj_name)

##切换数据集
DefaultAssay(scRNA) <- "RNA"

##计算线粒体和红细胞基因比例
scRNA[["percent.mt"]] <- PercentageFeatureSet(scRNA, pattern = "^MT-")
#计算红细胞比例
HB.genes <- c("HBA1","HBA2")
HB_m <- match(HB.genes, rownames(scRNA@assays$RNA)) 
HB.genes <- rownames(scRNA@assays$RNA)[HB_m] 
HB.genes <- HB.genes[!is.na(HB.genes)] 
scRNA[["percent.HB"]]<-PercentageFeatureSet(scRNA, features=HB.genes) 
#head(scRNA@meta.data)
col.num <- length(levels(as.factor(scRNA@meta.data$orig.ident)))

##绘制小提琴图
#所有样本一个小提琴图用group.by="proj_name"，每个样本一个小提琴图用group.by="orig.ident"
violin <-VlnPlot(scRNA, group.by = "proj_name",  
         features = c("nFeature_RNA", "nCount_RNA", "percent.mt","percent.HB"), 
         cols =rainbow(col.num), 
         pt.size = 0.01, #不需要显示点，可以设置pt.size = 0
         ncol = 4) + 
         theme(axis.title.x=element_blank(), axis.text.x=element_blank(), axis.ticks.x=element_blank()) 
ggsave("cluster1/vlnplot_before_qc.pdf", plot = violin, width = 12, height = 6) 
ggsave("cluster1/vlnplot_before_qc.png", plot = violin, width = 12, height = 6)  
plot1 <- FeatureScatter(scRNA, feature1 = "nCount_RNA", feature2 = "percent.mt")
plot2 <- FeatureScatter(scRNA, feature1 = "nCount_RNA", feature2 = "nFeature_RNA")
plot3 <- FeatureScatter(scRNA, feature1 = "nCount_RNA", feature2 = "percent.HB")
pearplot <- CombinePlots(plots = list(plot1, plot2, plot3), nrow=1, legend="none") 
ggsave("cluster1/pearplot_before_qc.pdf", plot = pearplot, width = 12, height = 5) 
ggsave("cluster1/pearplot_before_qc.png", plot = pearplot, width = 12, height = 5)

##设置质控标准
print(c("请输入允许基因数和核糖体比例，示例如下：", "minGene=500", "maxGene=4000", "pctMT=20"))
minGene=500
maxGene=3000
pctMT=10

##数据质控
scRNA <- subset(scRNA, subset = nFeature_RNA > minGene & nFeature_RNA < maxGene & percent.mt < pctMT)
col.num <- length(levels(as.factor(scRNA@meta.data$orig.ident)))
violin <-VlnPlot(scRNA, group.by = "proj_name",
         features = c("nFeature_RNA", "nCount_RNA", "percent.mt","percent.HB"), 
         cols =rainbow(col.num), 
         pt.size = 0.1, 
         ncol = 4) + 
         theme(axis.title.x=element_blank(), axis.text.x=element_blank(), axis.ticks.x=element_blank()) 
ggsave("QC/vlnplot_after_qc.pdf", plot = violin, width = 12, height = 6) 
ggsave("QC/vlnplot_after_qc.png", plot = violin, width = 12, height = 6)

质控后的结果：质控前的结果：

前后对比很明显，这也就说明了对数据的质控的重要性。

最后我所做的所有分析与教程的代码都会在我的个人公众号中，请打开微信搜索“生信学徒”进行关注，欢迎生信的研究人员和同学前来讨论分析。
ps：公众号刚刚建立比较简陋，但是该有的内容都不会少。

最后

以上就是有魅力菠萝为你收集整理的单细胞多样本多平台合并分析（二）的全部内容，希望文章能够帮你解决单细胞多样本多平台合并分析（二）所遇到的程序开发问题。

如果觉得靠谱客网站的内容还不错，欢迎将靠谱客网站推荐给程序员好友。