——标题:“5。Advanced Lab - Explore the Data " author: "Sonali Arora" output: BiocStyle::html_document: toc: true toc_depth: 2 vignette: > % \VignetteIndexEntry{5。Advanced Lab - Explore the Data} % \VignetteEngine{knitr::rmarkdown}——' ' ' {r style, echo = FALSE, results = 'asis'} BiocStyle::markdown() options(width=100, max.print=1000) knitr::opts_chunk$set(eval=as.logical(Sys. print=1000);采用“KNITR_EVAL”,“真正的”)),缓存= as.logical (Sys。采用“KNITR_CACHE”,“真正的”)),错误= FALSE)作者:Sonali Arora (sarora@fredhutch.org.）
日期:2015年7月20-22日
本课程中的材料需要R版本3.2.1和Biocumon V9.2 ##高级实验室的Biocultomonder - 探索该实验室中的数据，我们将浏览来自`R Biocpkg（“Airway”）的数据集，然后随后使用同样运行快速RNA-SEQ分析。步骤包括 - 加载数据包并使用基本访问者探索数据集 - 执行“RLOG`转换” - 评估哪些样本彼此相似 - 使用主成分分析（PCA） - 使用多维缩放（MDS）） - 总结该实验室的数据数据，该实验室中使用的数据是用地塞米松处理的气道平滑肌细胞的RNA-SEQ试验，一种具有抗炎作用的合成糖皮质激素类固醇。例如，在哮喘患者中使用糖皮质激素，以防止或减少气道的炎症。在实验中，用1微摩尔地塞米松处理了四次初级人气道平滑肌细胞系18小时。对于四种细胞系中的每一种，我们具有治疗和未处理的样品。实验的参考是：Hemes是，江X，瓦格纳P，胡河，王Q，Klanderman B，Whitaker RM，段Q，Lasky-Su J，Nikolos C，Jester W，Johnson M，Panettieri R JR，TantisiriKg，Weiss ST，Lu Q.“RNA-SEQ转录组分析将Cyrld2识别为糖皮质激素响应基因，调节气道平滑肌细胞中细胞因子功能。”Plos一个。2014年6月13日; 9（6）：E99625。 PMID: [24926665](http://www.ncbi.nlm.nih.gov/pubmed/24926665). GEO: [GSE52778](http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE52778). For our analysis, we wil use data from the data package `r Biocpkg("airway")`. ```{r load-data} library("airway") data(airway) ``` ## Solutions ### Answer 1 : Load the Data _Bioconductor_ software packages often define and use a custom class for their data object, which makes sure that all the needed data slots are consistently provided and fulfill the requirements. The data stored inside `r Biocpkg("airway")` is a *SummarizedExperiment* object. ```{r play} library("airway") data(airway) se <- airway se ``` For a *SummarizedExperiment* object, The `assay(s)` contains the matrix (or matrices) of summarized values, the `rowData` contains information about the genomic ranges, and the `colData` contains information about the samples or experiments. ```{r revise-se} head(assay(se)) colSums(assay(se)) colData(se) rowRanges(se) ``` In `r Biocpkg("DESeq2")`, the custom class is called *DESeqDataSet*. It is built on top of the *SummarizedExperiment* class. ```{r make-dds} library(DESeq2) dds <- DESeqDataSet(se, design = ~ cell + dex) ``` ### Answer 2 : rlog transformation Many common statistical methods for exploratory analysis of multidimensional data, especially methods for clustering and ordination (e.g., principal-component analysis and the like), work best for (at least approximately) homoskedastic data; this means that the variance of an observed quantity (here, the expression strength of a gene) does not depend on the mean. In RNA-Seq data, the variance grows with the mean.If one performs PCA (principal components analysis) directly on a matrix of normalized read counts, the result typically depends only on the few most strongly expressed genes because they show the largest absolute differences between samples. As a solution, DESeq2 offers the regularized-logarithm transformation, or rlog for short. See the help for ?rlog for more information and options. The function rlog returns a SummarizedExperiment object which contains the rlog-transformed values in its assay slot: ```{r do-rlog} rld <- rlog(dds) head(assay(rld)) ``` ### Answer 3 : Visualize the Data To assess overall similarity between samples: Which samples are similar to each other, which are different? Does this fit to the expectation from the experiment's design? We use the R function dist to calculate the Euclidean distance between samples. To avoid that the distance measure is dominated by a few highly variable genes, and have a roughly equal contribution from all genes, we use it on the rlog-transformed data ```{r dist} sampleDists <- dist( t( assay(rld) ) ) sampleDists ``` Note the use of the function t to transpose the data matrix. We need this because dist calculates distances between data rows and our samples constitute the columns. #### Heatmaps We visualize the sample-to-sample distances in a heatmap, using the function heatmap.2 from the gplots package. Note that we have changed the row names of the distance matrix to contain treatment type and patient number instead of sample ID, so that we have all this information in view when looking at the heatmap. ```{r message=FALSE} library("gplots") library("RColorBrewer") sampleDistMatrix <- as.matrix( sampleDists ) rownames(sampleDistMatrix) <- paste( rld$dex, rld$cell, sep="-" ) colors <- colorRampPalette( rev(brewer.pal(9, "Blues")) )(255) hc <- hclust(sampleDists) heatmap.2( sampleDistMatrix, Rowv=as.dendrogram(hc), symm=TRUE, trace="none", col=colors, margins=c(2,10), labCol=FALSE ) ``` #### PCA Another way to visualize sample-to-sample distances is a principal-components analysis (PCA). In this ordination method, the data points (i.e., here, the samples) are projected onto the 2D plane such that they spread out in the two directions which explain most of the differences in the data. The x-axis is the direction (or principal component) which separates the data points the most. The amount of the total variance which is contained in the direction is printed in the axis label. Here, we have used the function plotPCA which comes with DESeq2. The two terms specified by intgroup are the interesting groups for labelling the samples; they tell the function to use them to choose colors. ```{r pca} plotPCA(rld, intgroup = c("dex", "cell")) ``` #### MDS Another plot, very similar to the PCA plot, can be made using the multidimensional scaling (MDS) function in base R. This is useful when we don't have the original data, but only a matrix of distances. Here we have the MDS plot for the distances calculated from the rlog transformed counts: ```{r mds} library(ggplot2) mds <- data.frame(cmdscale(sampleDistMatrix)) mds <- cbind(mds, colData(rld)) qplot(X1,X2,color=dex,shape=cell,data=as.data.frame(mds)) ``` ### Answer 4 : Summarize the plots We see that the differences between cells are considerable, though not stronger than the differences due to treatment with dexamethasone. This shows why it will be important to account for this in differential testing by using a paired design ('paired', because each dex treated sample is paired with one untreated sample from the same cell line). We are already set up for this by using the design formula ~ cell + dex when setting up the data object in the beginning. ## References For a much detailed analysis see - [Case Study- How to build a SummarizedExperiment - airway dataset](//www.andersvercelli.com/packages/devel/data/experiment/vignettes/airway/inst/doc/airway.html) - [Exploring the Data using Machine Learning Techniques](//www.andersvercelli.com/help/course-materials/2015/SeattleApr2015/D_MachineLearning.html) ## What to not miss at BioC2015 ! If you liked this lab and want to learn more in this area, do not miss the following labs at BioC2015 - _Differential expression, manipulation, and visualization of RNA-seq reads_ by Mike Love. (Session 1, Tuesday, 1:00pm -2:45pm) - _Automated NGS workflows with systemPipeR running on clusters or single machines, with a focus on VAR-seq_ by Thomas Girke. (Session 4, Tuesday, 3:15pm - 5:00pm) ## `sessionInfo()` ```{r sessionInfo} sessionInfo() ```