Introduction to Multivariate Analysis of Gene Expression Data using MADE4

Aedin Culhane1

1Department of Data Science, Dana-Farber Cancer Institute, Department of Biostatistics, Harvard TH Chan School of Public Health

29 October 2024

Abstract

Vignette introduction function in the made4 package. This package is old and was originally designed for the analysis of microarray data. However most of the functions, such as bga, cia etc can be applied to any ’omics data. Some of these functions are avaialble in omicade4, mogsa and corral, and I am migrating this package into Bioconductor compliant package ;-) If you have found functions in made4 useful, and would like to assist, in updating it, please let me know. I’d be delighted.

Package

BiocStyle 2.34.0

1 Introduction

library(ade4)
library(made4)

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library(scatterplot3d)

The package made4 facilitates multivariate analysis of microarray gene expression data. The package provides a set of functions that utilise and extend multivariate statistical and graphical functions available in ade4, (Thioulouse et al. 1997) .
made4 accepts gene expression data is a variety of input formats, including Bioconductor formats, - SummarizedExperiment - ExpressionSet - data.frame - matrix and older microarray formats; ExpressionSet, marrayRaw

2 Installation

made4 requires the R package ade4. It should be installed automatically when you install made4. To install made4 from bioconductor

if (!requireNamespace("BiocManager", quietly=TRUE))
    install.packages("BiocManager")
BiocManager::install("made4")

3 Further help

The package made4 is described in more detail in the RNews newletter, December 2006.

Culhane AC and Thioulouse J. (2006) A multivariate approach to integrating datasets using made4 and ade4.R News, 6(5) 54-58. pdf

Extensive tutorials, examples and documentation on multivariate statistical methods are available from [the ade4 website] (http://pbil.univ-lyon1.fr/ADE-4) and ade4 user support
is available through the ADE4 mailing list.

This tutorial assumes a basic knowledge of R, but we have found that Emmanuel Paradis’s R for Beginners is a very good guide to those unfamiliar with R. This is [available at] (http://cran.r-project.org/doc/contrib/Paradis-rdebuts_en.pdf).

This documents assumes that data is normalized and preprocessed.

4 Citing

We are delighted if you use this package. Please do email us if you find a bug or have a suggestion. We would be very grateful if you could cite:

Culhane AC, Thioulouse J, Perriere G, Higgins DG.(2005) MADE4: an R package for multivariate analysis of gene expression data. Bioinformatics 21(11): 2789-90.

5 Quickstart

We will very briefly demonstrate some of the functions in made4. To do this we will use a small dataset that is available in made4. This dataset Khan contains gene expression profiles of four types of small round blue cell tumours of childhood (SRBCT) published by Khan et al. (2001). This is a subset of the published dataset. It contains gene expression levels for 306 genes for 64 patient samples. Load the necessary R packages and dataset.

 library(made4)
 library(ade4)
 data(khan)

This experiment studied gene expression in patient with four types of SRBCT. These were neuroblastoma (NB), rhabdomyosarcoma (RMS), Burkitt lymphoma, a subset of non-Hodgkin lymphoma (BL), and the Ewing family of tumours (EWS). Gene expression profiles from both tumour biopsy and cell line samples were obtained and are contained in this dataset. In this study data were divided into a training set of 64 samples, and a blind test dataset. These 2 dataset are called khan$train and khan$test. Have a look at the data. For this example we will just example the training dataset.

names(khan)

## [1] "train"                "test"                 "train.classes"       
## [4] "test.classes"         "annotation"           "gene.labels.imagesID"
## [7] "cellType"

k.data<-khan$train
k.class<-khan$train.classes

5.1 Overview

The made4 function overview() provides a quick way to get an overview or feel for data. overview() will draw a boxplot, histogram and dendrogram of a hierarchical analysis. Hierarchical clustering is produced using average linkage clustering with a Pearson correlation measure of similarity (Eisen et al. 1998) This gives a quick first glance at the data.

overview(k.data)

Often its useful to label the samples using a class vector or covariate of interest, in this case, the tumour type (EWS, BL, NB or RMS).

overview(k.data, labels=k.class)

$\label{fig:fig1}Overview of Khan data.$

Figure 1: Overview of Khan data

Figure 1: A) dendrogram showing results of average linkage clustering, B) boxplot and C) histrogram.

Often one will known classes in the data (eg Normal v Treatment, or different tumor types). We can insert a class colourbar under the dendrogram, and colour the boxplot.

overview(k.data, classvec=k.class, labels=k.class)

$\label{fig:fig2}Overview of Khan data.$

Figure 2: Overview of Khan data

dendrogram showing results of average linkage clustering, B) boxplot and C) histrogram. In this case we have added a vector of class (classvec) to color the overview by class membership.

6 Prinipcal Component, Correspondence Analysis

The function ord simplifies the running of ordination methods such as principal component, correspondence or non-symmetric correspondence analysis. It provides a wrapper which can call each of these methods in ade4. To run a correspondence analysis (Fellenberg et al. 2001) on this dataset.

k.coa<- ord(k.data, type="coa")

Output from ord is a list of length 2, containing the ordination results ($ord) and a factor ($fac) if input. The ordination results (k.coa$ord) contain a list of results (of length 12) which includes the eigenvalues ($eig) and the new column coordinates ($co) and the row (line) coordinatein $li. Hence we can visualise the projected coordinations of the genes ($li, 306 genes) and array samples ($co, 64 microarray samples).

names(k.coa)

## [1] "ord" "fac"

summary(k.coa$ord)

## Class: coa dudi
## Call: dudi.coa(df = data.tr, scannf = FALSE, nf = ord.nf)
## 
## Total inertia: 1.011
## 
## Eigenvalues:
##     Ax1     Ax2     Ax3     Ax4     Ax5 
## 0.17130 0.13831 0.10317 0.05995 0.04965 
## 
## Projected inertia (%):
##     Ax1     Ax2     Ax3     Ax4     Ax5 
##  16.947  13.683  10.207   5.931   4.912 
## 
## Cumulative projected inertia (%):
##     Ax1   Ax1:2   Ax1:3   Ax1:4   Ax1:5 
##   16.95   30.63   40.84   46.77   51.68 
## 
## (Only 5 dimensions (out of 63) are shown)

6.1 Visualising Results

There are many functions in ade4 and made4 for visualising results from ordination analysis. The simplest way to view the results produced by ord is to use plot. plot(k.ord) will draw a plot of the eigenvalues, along with plots of the variables (genes) and a plot of the cases (microarray samples). In this example Microarray samples are colour-coded using the classvec khan$train.classes which is saved as k.class.

k.class

##  [1] EWS    EWS    EWS    EWS    EWS    EWS    EWS    EWS    EWS    EWS   
## [11] EWS    EWS    EWS    EWS    EWS    EWS    EWS    EWS    EWS    EWS   
## [21] EWS    EWS    EWS    BL-NHL BL-NHL BL-NHL BL-NHL BL-NHL BL-NHL BL-NHL
## [31] BL-NHL NB     NB     NB     NB     NB     NB     NB     NB     NB    
## [41] NB     NB     NB     RMS    RMS    RMS    RMS    RMS    RMS    RMS   
## [51] RMS    RMS    RMS    RMS    RMS    RMS    RMS    RMS    RMS    RMS   
## [61] RMS    RMS    RMS    RMS   
## Levels: EWS BL-NHL NB RMS

plot(k.coa, classvec=k.class, genecol="grey3")

Figure 2 Correspondence analysis of Khan dataset. A. plot of the eigenvalues, B. projection of microarray samples from patient with tumour types EWS (red), BL(blue), NB (green) or RMS (brown), C. projection of genes (gray filled circles) and D. biplot showing both genes and samples. Samples and genes with a strong associated are projected in the same direction from the origin. The greater the distance from the origin the stronger the association.

Genes and array projections can also be plotted using plotgenes and plotarrays. The function s.groups required a character vector or factor that indicates the groupings or classes (classvec) and allowed groups to be coloured in different colours. For example, to plot microarray samples (cases),

plotgenes(k.coa)

To plot microarray samples, colour by group (tumour type) as specified by khan$train.classes

plotarrays(k.coa, arraylabels=k.class)

## [1] "Need to specify groups"

Alternative you can run these analysis and give a class vector to ord and it will automatically colour samples by this class vector

k.coa2<-ord(k.data, classvec=k.class)
plot(k.coa2)

Plot gene projections without labels (clab=0). Typically there are a large number of genes, thus it is not feasible to label all of these. The function plotgenes is more useful to use if you wish to add labels when there are lots of variables (genes)

The gene projections can be also visualised with plotgenes. The number of genes that are labelled at the end of the axis can be defined. The default is 10.

plotgenes(k.coa, n=5, col="red")

By default the variables (genes) are labelled with the rownames of the matrix. Typically these are spot IDs or Affymetrix accession numbers which are not very easy to interpret. But these can be easily labeled by your own labels. For example its often useful to labels using HUGO gene symbols. We find the Bioconductor annotate or biomaRt annotation packages are useful for this.

In this example we provide annotation from the Source database in khan$annotation. The gene symbol are in the vector khan$annotation$Symbol. (In this case its a factor)

gene.symbs<- khan$annotation$Symbol 
gene.symbs[1:4]

## [1] FDFT1 LYN   CKS2  MT1X 
## 1944 Levels:  101F6 182-FIP 7h3 A2LP AADAC AAMP ABCC3 ABCE1 ABCF1 ABCF2 ... ZWINT

plotgenes(k.coa, n=10, col="red", genelabels=gene.symbs)

Figure 3 Projection of genes (filled circles) in Correspondence analysis of Khan dataset. The genes at the ends of each of the axes are labelled with HUGO gene symbols.

To get a list of variables at the end of an axes, use topgenes. For example, to get a list of the 5 genes at the negative and postive end of axes 1.

topgenes(k.coa, axis = 1, n=5)

To only the a list of the genes (default 10 genes) at the negative end of the first axes

topgenes(k.coa, labels=gene.symbs, end="neg")

##  [1] "PTPN13"  "OLFM1"   "TNFAIP6" "GYG2"    "CAV1"    "MYC"     "FVT1"   
##  [8] "FCGRT"   "TUBB5"   "MYC"

Two character vectors can be compared using (the very poorly named function) comparelists

To visualise the arrays (or genes) in 3D either use do3d or html3d. do3d is a wrapper for scatterplot3d, but is modified so that groups can be coloured.

do3d(k.coa$ord$co, classvec=k.class, cex.symbols=3)

html3d produces a “pdb” output which can be visualised using rasmol or chime, a free interface for colour, rotating, zooming 3D graphs. The output from Output from html3D can be rotated and visualised on web browsers that can support chime (or a pdb viewer)

html3D(k.coa$ord$co, k.class, writehtml=TRUE)

Figure 3: Output from html3D

6.2 explor

It is also worth exploring the package explor which provides a nice R Shiny interface for browsing results from made4 and ade4. It is available from CRAN or from juba.github.io

6.3 Classification and Class Prediction using Between Group Analysis

Between Group Analysis (BGA) is a supervised PCA method (Dolédec and Chessel 1987) for classification/prediction. The basis of BGA is to ordinate the groups rather than the individual samples.

In tests on two microarray gene expression datasets, BGA performed comparably to supervised classification methods, including support vector machines and artifical neural networks (Culhane et al. 2002). To train a dataset, use bga, the projection of test data can be assessed using suppl. One leave out cross validation can be performed using bga.jackknife. See the BGA vignette for more details on this method.

k.bga<-bga(k.data, type="coa", classvec=k.class)

plot(k.bga, genelabels=gene.symbs) # Use the gene symbols earlier

Figure 5 Between group analysis of Khan dataset. A. Between.graph of the microarray samples, showing their separation on the discriminating BGA axes, B. Scatterplot of the first 2 axes of microarray samples, coloured by their class, C. graph of positions of genes on the same axis. Genes at the ends of the axis are most discriminating for that group

Sometimes its useful to visualise 1 axes of an analysis. To do this use graph1D or between.graph. The latter function is specifically for visualising results from a bga as it shows the separation of classes achieved.

between.graph(k.bga, ax=1)  # Show the separation on the first axes(ax)

6.4 Meta-analysis of microarray gene expression

Coinertia analysis cia (Dolédec S and Chessel D 1994) has been successfully applied to the cross-platform comparison of microarray gene expression datasets (Culhane, Perrière, and Higgins 2003, @meng_multivariate_2014, @meng_integrative_2016, @meng_dimension_2016), . CIA is a multivariate method that identifies trends or co-structure in the variance of multiple datasets which contain the same samples. That is either the rows or the columns of a matrix must be “matchable”. CIA can be applied to datasets where the number of variables (genes) far exceeds the number of samples (arrays) such is the case with microarray analyses. cia calls coinertia in the ade4 package. See the CIA vignette for more details on this method.

There are extended version of CIA in the Bioconducor packages mogsa and omicade4 (Meng et al. 2014, @meng_integrative_2016, @meng_dimension_2016)

# Example data are "G1_Ross_1375.txt" and "G5_Affy_1517.txt"
data(NCI60)
coin <- cia(NCI60$Ross, NCI60$Affy)
names(coin)

## [1] "call"      "coinertia" "coa1"      "coa2"

coin$coinertia$RV

## [1] 0.7859656

The RV coefficient $RV which is 0.786 in this instance, is a measure of global similarity between the datasets.
The greater (scale 0-1) the better.

plot(coin, classvec=NCI60$classes[,2], clab=0, cpoint=3)

Figure 6 Coinertia analysis of NCI 60 cell line Spotted and Affymetrix gene expression dataset. The same 60 cell lines were analysed by two different labs on a spotted cDNA array (Ross) and an affymetrix array (Affy). The Ross dataset contains 1375 genes, and the affy dataset contains 1517. There is little overlap betwen the genes represented on these platforms. CIA allows visualisation of genes with similar expression patterns across platforms. A) shows a plot of the 60 microarray samples projected onto the one space. The 60 circles represent dataset 1 (Ross) and the 60 arrows represent dataset 2 (affy). Each circle and arrow are joined by a line, the length of which is proportional to the divergence between that samples in the two datasets. The samples are coloured by cell type. B) The gene projections from datasets 1 (Ross), C) the gene projections from dataset 2 (Affy). Genes and samples projected in the same direction from the origin show genes that are expressed in those samples. See vingette for more help on interpreting these plots.

7 Functions in made4

7.1 Data Input

function	description
isDataFrame	converts matrix, data.frame, ExpressionSet,
	SummarizedExperiment, marrayRaw, microarray or
	RNAseq gene expression or any matrix data input
	into a data frame suitable for analysis in ADE4.
	The rows and columns are expected to contain the
	variables (genes) and cases (array samples)
overview	Draw boxplot, histogram and hierarchical tree of gene
	expression data. This is useful only for a first glance
	at data.

7.2 Example datasets provides with made4

function	description
khan	Microarray gene expression dataset from Khan et al., 2001
NCI60	Microarray gene expression profiles of NCI 60 cell lines

7.3 Classification and class prediction using Between Group Analysis

function	description
bga	Between group analysis
bga.jackknife	Jackknife between group analysis
randomiser	Randomly reassign training and test samples
bga.suppl	Between group analysis with supplementary data projection
suppl	Projection of supplementary data onto axes from
	a between group analysis
plot.bga	Plot results of between group analysis
between.graph	Plot 1D graph of results from between group analysis

7.4 Meta analysis of two or more datasets using Coinertia Analysis

function	description
cia	Coinertia analysis: Explore the covariance between two datasets
plot.cia	Plot results of coinertia analysis

7.5 Graphical Visualisation of results: 1D Visualisation

function	description
graph1D	Plot 1D graph of axis from multivariate analysis
between.graph	Plot 1D graph of results from between group analysis
commonMap	Highlight common points between two 1D plots
heatplot	Draws heatmap with dendrograms (of eigenvalues)

7.6 Graphical Visualisation of results: 2D Visualisation

function	description
plotgenes	Graph xy plot of variable (gene) projections from PCA or COA. Only label variables at ends of axes
plotarrays	Graph xy plot of case (samples) projections from PCA or COA,and colour by group
plot.bga	Plot results of between group analysis using plotgenes, s.groups and s.var
plot.cia	Plot results of coinertia analysis showing s.match.col, and plotgenes
s.var	Use plotarrays instead. Graph xy plot of variables (genes or arrays). Derived from ADE4 graphics module s.label.
s.groups	Use plotarrays instead. Graph xy plot of groups of variables (genes or arrays) and colour by group. Derived from ADE4 graphics module s.class
s.match.col	Use plotarrays instead. Graph xy plot of 2 sets of variables (normally genes) from CIA. Derived from ADE4 graphics module s.match

7.7 Graphical Visualisation of results: 3D Visualisation

function	description
do3d	Generate a 3D xyz graph using scatterplot3d
rotate3d	Generate multiple 3D graphs using do3d in which each graph is rotated
html3D	Produce web page with a 3D graph that can be viewed using Chime web browser plug-in, and/or a pdb file that can be viewed using Rasmol

7.8 Interpretation of results

function	description
topgenes	Returns a list of variables at the ends (positive, negative or both) of an axis
sumstats	Summary statistics on xy co-ordinates, returns the slopes and distance from origin of each co-ordinate
comparelists	Return the intersect, difference and union between 2 vectors (poorly named. it does not work on a list object)
print.comparelists	Prints the results of comparelists

References

Culhane, Aedín C, Guy Perrière, Elizabeth C Considine, Thomas G Cotter, and Desmond G Higgins. 2002. “Between-Group Analysis of Microarray Data.” Bioinformatics (Oxford, England) 18 (12): 1600–1608. http://www.ncbi.nlm.nih.gov.ezp-prod1.hul.harvard.edu/pubmed/12490444.

Culhane, Aedín C, Guy Perrière, and Desmond G Higgins. 2003. “Cross-Platform Comparison and Visualisation of Gene Expression Data Using Co-Inertia Analysis.” BMC Bioinformatics 4 (November): 59. https://doi.org/10.1186/1471-2105-4-59.

Dolédec, Sylvain, and Daniel Chessel. 1987. “Rythmes Saisonniers et Composantes Stationnelles En Milieu Aquatique. I: Description d’un Plan d’observation Complet Par Projection de Variables.” In.

Dolédec S, and Chessel D. 1994. “Co-Inertia Analysis: An Alternative Method for Studying Species-Environment Relationships.” Freshwater Biology 31: 277–94.

Eisen, Michael B., Paul T. Spellman, Patrick O. Brown, and David Botstein. 1998. “Cluster Analysis and Display of Genome-Wide Expression Patterns.” Proceedings of the National Academy of Sciences 95 (25): 14863–8. https://www.pnas.org/content/95/25/14863.

Fellenberg, K, N C Hauser, B Brors, A Neutzner, J D Hoheisel, and M Vingron. 2001. “Correspondence Analysis Applied to Microarray Data.” Proceedings of the National Academy of Sciences of the United States of America 98 (19): 10781–6. https://doi.org/10.1073/pnas.181597298.

Meng, Chen, and Aedin Culhane. 2016. “Integrative Exploratory Analysis of Two or More Genomic Datasets.” Methods in Molecular Biology (Clifton, N.J.) 1418: 19–38. https://doi.org/10.1007/978-1-4939-3578-9_2.

Meng, Chen, Bernhard Kuster, Aedín C. Culhane, and Amin Moghaddas Gholami. 2014. “A Multivariate Approach to the Integration of Multi-Omics Datasets.” BMC Bioinformatics 15 (May): 162. https://doi.org/10.1186/1471-2105-15-162.

Meng, Chen, Oana A. Zeleznik, Gerhard G. Thallinger, Bernhard Kuster, Amin M. Gholami, and Aedín C. Culhane. 2016. “Dimension Reduction Techniques for the Integrative Analysis of Multi-Omics Data.” Briefings in Bioinformatics 17 (4): 628–41. https://doi.org/10.1093/bib/bbv108.

Thioulouse, Jean, Daniel Chessel, Sylvain Dole´dec, and Jean-Michel Olivier. 1997. “ADE-4: A Multivariate Analysis and Graphical Display Software.” Statistics and Computing 7 (1): 75–83. https://doi.org/10.1023/A:1018513530268.