### Create: Jianming Zeng
### Date: 2019-04-02 21:59:01
### Email: jmzeng1314@163.com
rm(list=ls())
options(stringsAsFactors = F)
Rdata_dir='../Rdata/'
Figure_dir='../figures/'
# 加载上一步从RTCGA.miRNASeq包里面提取miRNA表达矩阵和对应的样本临床信息。
# 见 //www.greatytc.com/p/a5f687d2e7b7
load( file =
file.path(Rdata_dir,'TCGA-KIRC-miRNA-example.Rdata')
)
dim(expr)
dim(meta)
# 可以看到是 537个病人，但是有593个样本，每个样本有 552个miRNA信息。
# 当然，这个数据集可以下载原始测序数据进行重新比对，可以拿到更多的miRNA信息
# 这里需要解析TCGA数据库的ID规律，来判断样本归类问题。
group_list=ifelse(as.numeric(substr(colnames(expr),14,15)) < 10,'tumor','normal') ##经验
table(group_list) #71个normal，522个tumor
exprSet=na.omit(expr)
source('../functions.R')
DESeq2包、edgeR包和limma包均可获取DEGs，下面依次展示
### Firstly run DESeq2
if(T){
library(DESeq2)
(colData <- data.frame(row.names=colnames(exprSet),
group_list=group_list) )
dds <- DESeqDataSetFromMatrix(countData = exprSet,
colData = colData,
design = ~ group_list)
tmp_f=file.path(Rdata_dir,'TCGA-KIRC-miRNA-DESeq2-dds.Rdata')
if(!file.exists(tmp_f)){
dds <- DESeq(dds)
save(dds,file = tmp_f)
}
load(file = tmp_f)
res <- results(dds,
contrast=c("group_list","tumor","normal"))
resOrdered <- res[order(res$padj),]
head(resOrdered)
DEG =as.data.frame(resOrdered)
DESeq2_DEG = na.omit(DEG)
nrDEG=DESeq2_DEG[,c(2,6)]
colnames(nrDEG)=c('log2FoldChange','pvalue')
draw_h_v(exprSet,nrDEG,'DEseq2',group_list,1)
}
PCA
DEG_top50_heatmap
volcano
### Then run edgeR
###
### ---------------
if(T){
library(edgeR)
d <- DGEList(counts=exprSet,group=factor(group_list))
keep <- rowSums(cpm(d)>1) >= 2
table(keep)
d <- d[keep, , keep.lib.sizes=FALSE]
d$samples$lib.size <- colSums(d$counts)
d <- calcNormFactors(d)
d$samples
dge=d
design <- model.matrix(~0+factor(group_list))
rownames(design)<-colnames(dge)
colnames(design)<-levels(factor(group_list))
dge=d
dge <- estimateGLMCommonDisp(dge,design)
dge <- estimateGLMTrendedDisp(dge, design)
dge <- estimateGLMTagwiseDisp(dge, design)
fit <- glmFit(dge, design)
# https://www.biostars.org/p/110861/
lrt <- glmLRT(fit, contrast=c(-1,1))
nrDEG=topTags(lrt, n=nrow(dge))
nrDEG=as.data.frame(nrDEG)
head(nrDEG)
edgeR_DEG =nrDEG
nrDEG=edgeR_DEG[,c(1,5)]
colnames(nrDEG)=c('log2FoldChange','pvalue')
draw_h_v(exprSet,nrDEG,'edgeR',group_list,1)
}
PCA
heatmap
volcano
### Lastly run voom from limma
if(T){
suppressMessages(library(limma))
design <- model.matrix(~0+factor(group_list))
colnames(design)=levels(factor(group_list))
rownames(design)=colnames(exprSet)
design
dge <- DGEList(counts=exprSet)
dge <- calcNormFactors(dge)
logCPM <- cpm(dge, log=TRUE, prior.count=3)
v <- voom(dge,design,plot=TRUE, normalize="quantile")
fit <- lmFit(v, design)
group_list
cont.matrix=makeContrasts(contrasts=c('tumor-normal'),levels = design)
fit2=contrasts.fit(fit,cont.matrix)
fit2=eBayes(fit2)
tempOutput = topTable(fit2, coef='tumor-normal', n=Inf)
DEG_limma_voom = na.omit(tempOutput)
head(DEG_limma_voom)
nrDEG=DEG_limma_voom[,c(1,4)]
colnames(nrDEG)=c('log2FoldChange','pvalue')
draw_h_v(exprSet,nrDEG,'limma',group_list,1)
}
PCA
heatmap
volcano
tmp_f=file.path(Rdata_dir,'TCGA-KIRC-miRNA-DEG_results.Rdata')
if(file.exists(tmp_f)){
save(DEG_limma_voom,DESeq2_DEG,edgeR_DEG, file = tmp_f)
}else{
load(file = tmp_f)
}
nrDEG1=DEG_limma_voom[,c(1,4)]
colnames(nrDEG1)=c('log2FoldChange','pvalue')
nrDEG2=edgeR_DEG[,c(1,5)]
colnames(nrDEG2)=c('log2FoldChange','pvalue')
nrDEG3=DESeq2_DEG[,c(2,6)]
colnames(nrDEG3)=c('log2FoldChange','pvalue')
mi=unique(c(rownames(nrDEG1),rownames(nrDEG1),rownames(nrDEG1)))
lf=data.frame(lf1=nrDEG1[mi,1],
lf2=nrDEG2[mi,1],
lf3=nrDEG3[mi,1])
cor(na.omit(lf))
[图片上传中...(image.png-f55ef-1557501086273-0)]
# 可以看到采取不同R包，会有不同的归一化算法，这样算到的logFC会稍微有差异。而且up&down基因数量也有差别
image.png
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