rnaseqGene初探

这次偶然发现了处理RNA-seq的新神器，首先附上地址：http://www.bioconductor.org/packages/devel/workflows/html/rnaseqGene.html

其中我比较喜欢的是降维这一部分和去除批次效应这一部分

降维

去除批次效应

1.数据准备

在说明文档里，作者采用的是salmon进行定量的

library("airway")
dir <- system.file("extdata", package="airway", mustWork=TRUE)
list.files(dir)

那么我们的目录里面包括

csvfile <- file.path(dir, "sample_table.csv")
coldata <- read.csv(csvfile, row.names=1, stringsAsFactors=FALSE)

coldata <- coldata[1:2,]
coldata$names <- coldata$Run
coldata$files <- file.path(dir, "quants", coldata$names, "quant.sf.gz")

由于salmon的output为了让数据包更小，quant.sf往往采用.gz的方式压缩，当然也可能存在quant.sf，两种形式都可以存在

se <- tximeta(coldata)
gse <- summarizeToGene(se)

2.差异表达

我们先可以采用如下命令看看数据对象长什么样

assayNames(gse)
head(assay(gse), 3)
colSums(assay(gse))
rowRanges(gse)
seqinfo(rowRanges(gse))
colData(gse)

然后设置分组

gse$cell <- gse$donor
gse$dex <- gse$condition
# when renaming levels, the order must be preserved!
levels(gse$dex) <- c("untrt", "trt")

gse$donor

gse$condition

其中

# when renaming levels, the order must be preserved!
levels(gse$dex) <- c("untrt", "trt")

可以用magrittr包的函数代替

library("magrittr")
gse$dex %<>% relevel("untrt")

接下来就是构建dds对象

library("DESeq2")
dds <- DESeqDataSet(gse, design = ~ cell + dex)

如果想看看表达矩阵，那么：

countdata <- round(assays(gse)[["counts"]])
head(countdata, 3)

3.可视化

3.1 热图

我们先画个聚类热图看看

vsd <- vst(dds, blind = FALSE)
sampleDists <- dist(t(assay(vsd)))

library("pheatmap")
library("RColorBrewer")

sampleDistMatrix <- as.matrix( sampleDists )
rownames(sampleDistMatrix) <- paste( vsd$dex, vsd$cell, sep = " - " )
colnames(sampleDistMatrix) <- NULL
colors <- colorRampPalette( rev(brewer.pal(9, "Blues")) )(255)
pheatmap(sampleDistMatrix,
         clustering_distance_rows = sampleDists,
         clustering_distance_cols = sampleDists,
         col = colors)

或者换种写法

library("PoiClaClu")
poisd <- PoissonDistance(t(counts(dds)))

samplePoisDistMatrix <- as.matrix( poisd$dd )
rownames(samplePoisDistMatrix) <- paste( dds$dex, dds$cell, sep=" - " )
colnames(samplePoisDistMatrix) <- NULL
pheatmap(samplePoisDistMatrix,
         clustering_distance_rows = poisd$dd,
         clustering_distance_cols = poisd$dd,
         col = colors)

3.2 降维

首先是PCA

vsd <- vst(dds, blind = FALSE)
sampleDists <- dist(t(assay(vsd)))
plotPCA(vsd, intgroup = c("dex", "cell"))

那么我们还可以提取降维后的PC1和PC2的坐标

pcaData <- plotPCA(vsd, intgroup = c( "dex", "cell"), returnData = TRUE)
pcaData

然后我们就可以随心所欲的画图了，比方说双分组：

ggplot(pcaData, aes(x = PC1, y = PC2, color = dex, shape = cell)) +
  geom_point(size =3) +
  xlab(paste0("PC1: ", percentVar[1], "% variance")) +
  ylab(paste0("PC2: ", percentVar[2], "% variance")) +
  coord_fixed() +
  ggtitle("PCA with VST data")

接着是广义的PCA，什么时候用广义的PCA呢？当我们的数据不满足于正态分布的时候（比方说，over-dispersed count data），我们才用广义PCA

library("glmpca")
gpca <- glmpca(counts(dds), L=2)
gpca.dat <- gpca$factors
gpca.dat$dex <- dds$dex
gpca.dat$cell <- dds$cell

ggplot(gpca.dat, aes(x = dim1, y = dim2, color = dex, shape = cell)) +
  geom_point(size =3) + coord_fixed() + ggtitle("glmpca - Generalized PCA")

接着是MDS降维

mds <- as.data.frame(colData(vsd))  %>%
         cbind(cmdscale(sampleDistMatrix))
ggplot(mds, aes(x = `1`, y = `2`, color = dex, shape = cell)) +
  geom_point(size = 3) + coord_fixed() + ggtitle("MDS with VST data")

mdsPois <- as.data.frame(colData(dds)) %>%
   cbind(cmdscale(samplePoisDistMatrix))
ggplot(mdsPois, aes(x = `1`, y = `2`, color = dex, shape = cell)) +
  geom_point(size = 3) + coord_fixed() + ggtitle("MDS with PoissonDistances")

4.差异表达

dds <- DESeq(dds)
res <- results(dds)

提取对应分组的差异表达

res <- results(dds, contrast=c("dex","trt","untrt"))
summary(res)
res.05 <- results(dds, alpha = 0.05)
table(res.05$padj < 0.05)

选取差异表达最显著的基因看各组表达量情况

topGene <- rownames(res)[which.min(res$padj)]

library("ggbeeswarm")
geneCounts <- plotCounts(dds, gene = topGene, intgroup = c("dex","cell"),
                         returnData = TRUE)
ggplot(geneCounts, aes(x = dex, y = count, color = cell)) +
  scale_y_log10() +  geom_beeswarm(cex = 3)

5. 基因聚类

library("genefilter")
topVarGenes <- head(order(rowVars(assay(vsd)), decreasing = TRUE), 20)

mat  <- assay(vsd)[ topVarGenes, ]
mat  <- mat - rowMeans(mat)
anno <- as.data.frame(colData(vsd)[, c("cell","dex")])
pheatmap(mat, annotation_col = anno)

6.注释

将基因ID注释成基因名称

library("AnnotationDbi")
library("org.Hs.eg.db")

ens.str <- substr(rownames(res), 1, 15)
res$symbol <- mapIds(org.Hs.eg.db,
                     keys=ens.str,
                     column="SYMBOL",
                     keytype="ENSEMBL",
                     multiVals="first")
res$entrez <- mapIds(org.Hs.eg.db,
                     keys=ens.str,
                     column="ENTREZID",
                     keytype="ENSEMBL",
                     multiVals="first")

7. 去除批次效应

去除批次效应有两个R包可以完成，sva和RUVSeq

7.1. sva

library("sva")

dat  <- counts(dds, normalized = TRUE)
idx  <- rowMeans(dat) > 1
dat  <- dat[idx, ]
mod  <- model.matrix(~ dex, colData(dds))
mod0 <- model.matrix(~   1, colData(dds))
svseq <- svaseq(dat, mod, mod0, n.sv = 2)

ddssva <- dds
ddssva$SV1 <- svseq$sv[,1]
ddssva$SV2 <- svseq$sv[,2]
design(ddssva) <- ~ SV1 + SV2 + dex

7.2 RUV

library("RUVSeq")

set <- newSeqExpressionSet(counts(dds))
idx  <- rowSums(counts(set) > 5) >= 2
set  <- set[idx, ]
set <- betweenLaneNormalization(set, which="upper")
not.sig <- rownames(res)[which(res$pvalue > .1)]
empirical <- rownames(set)[ rownames(set) %in% not.sig ]
set <- RUVg(set, empirical, k=2)

ddsruv <- dds
ddsruv$W1 <- set$W_1
ddsruv$W2 <- set$W_2
design(ddsruv) <- ~ W1 + W2 + dex