GSVA: gene set variation analysis

Robert Castelo1*, Axel Klenk1** and Justin Guinney2***

1Dept. of Medicine and Life Sciences, Universitat Pompeu Fabra, Barcelona, Spain
2Tempus Labs, Inc.

*robert.castelo@upf.edu
**axelvolker.klenk@upf.edu
***justin.guinney@tempus.com

15 April 2024

Abstract

Gene set variation analysis (GSVA) is a particular type of gene set enrichment method that works on single samples and enables pathway-centric analyses of molecular data by performing a conceptually simple but powerful change in the functional unit of analysis, from genes to gene sets. The GSVA package provides the implementation of four single-sample gene set enrichment methods, concretely zscore, plage, ssGSEA and its own called GSVA. While this methodology was initially developed for gene expression data, it can be applied to other types of molecular profiling data. In this vignette we illustrate how to use the GSVA package with bulk microarray and RNA-seq expression data.

Package

GSVA 1.50.5

License: GPL (>= 2)

1 Quick start

GSVA is an R package distributed as part of the Bioconductor project. To install the package, start R and enter:

install.packages("BiocManager")
BiocManager::install("GSVA")

Once GSVA is installed, it can be loaded with the following command.

library(GSVA)

Given a gene expression data matrix, which we shall call X, with rows corresponding to genes and columns to samples, such as this one simulated from random Gaussian data:

p <- 10000 ## number of genes
n <- 30    ## number of samples
## simulate expression values from a standard Gaussian distribution
X <- matrix(rnorm(p*n), nrow=p,
            dimnames=list(paste0("g", 1:p), paste0("s", 1:n)))
X[1:5, 1:5]
           s1          s2         s3        s4          s5
g1 -1.0144154 -0.09912636 -0.7708663  2.249459 -0.44427793
g2 -2.2082513  1.74329073 -0.2462014  2.492418  0.04811288
g3  1.6454552  0.02575172  0.4386260 -0.205889  0.14453931
g4 -0.3485902 -0.20907804 -0.4149486 -1.079936  0.59952414
g5  0.1244553 -0.49403006 -1.1104565  1.260907 -0.27976054

Given a collection of gene sets stored, for instance, in a list object, which we shall call gs, with genes sampled uniformly at random without replacement into 100 different gene sets:

## sample gene set sizes
gs <- as.list(sample(10:100, size=100, replace=TRUE))
## sample gene sets
gs <- lapply(gs, function(n, p)
                   paste0("g", sample(1:p, size=n, replace=FALSE)), p)
names(gs) <- paste0("gs", 1:length(gs))

We can calculate GSVA enrichment scores as follows. First we should build a parameter object for the desired methodology. Here we illustrate it with the GSVA algorithm of Hänzelmann, Castelo, and Guinney (2013) by calling the function gsvaParam(), but other parameter object constructor functions are available; see in the next section below.

gsvaPar <- gsvaParam(X, gs)
gsvaPar
A GSVA::gsvaParam object
expression data:
  matrix [10000, 30]
    rows: g1, g2, ..., g10000 (10000 total)
    cols: s1, s2, ..., s30 (30 total)
using assay: none
gene sets:
  list
    names: gs1, gs2, ..., gs100 (100 total)
    unique identifiers: g1251, g8931, ..., g5943 (4382 total)
gene set size: [1, Inf]
kcdf: Gaussian
tau: 1
maxDiff: TRUE
absRanking: FALSE

The first argument to the gsvaParam() function constructing this parameter object is the gene expression data matrix, and the second is the collection of gene sets. In this example, we provide expression data and gene sets into base R matrix and list objects, respectively, to the gsvaParam() function, but it can take also different specialized containers that facilitate the access and manipulation of molecular and phenotype data, as well as their associated metadata.

Second, we call the gsva() function with the parameter object as first argument. Other additional arguments to the gsva() function are verbose to control progress reporting and BPPPARAM to perform calculations in parallel through the package BiocParallel.

gsva.es <- gsva(gsvaPar, verbose=FALSE)
dim(gsva.es)
[1] 100  30
gsva.es[1:5, 1:5]
            s1          s2           s3            s4          s5
gs1  0.1228032  0.42986391 -0.162519563  0.0327360096  0.09614379
gs2  0.2044804 -0.08906806 -0.086573606 -0.0520060220  0.02519241
gs3 -0.1923746 -0.08814664  0.009773796 -0.0125096426  0.10378777
gs4 -0.1895404  0.06149931 -0.154111954 -0.0007291551 -0.02929820
gs5  0.0193845  0.11986674  0.082663131 -0.2535587638  0.08792097

2 Introduction

Gene set variation analysis (GSVA) provides an estimate of pathway activity by transforming an input gene-by-sample expression data matrix into a corresponding gene-set-by-sample expression data matrix. This resulting expression data matrix can be then used with classical analytical methods such as differential expression, classification, survival analysis, clustering or correlation analysis in a pathway-centric manner. One can also perform sample-wise comparisons between pathways and other molecular data types such as microRNA expression or binding data, copy-number variation (CNV) data or single nucleotide polymorphisms (SNPs).

The GSVA package provides an implementation of this approach for the following methods:

plage (Tomfohr, Lu, and Kepler 2005). Pathway level analysis of gene expression (PLAGE) standardizes expression profiles over the samples and then, for each gene set, it performs a singular value decomposition (SVD) over its genes. The coefficients of the first right-singular vector are returned as the estimates of pathway activity over the samples. Note that, because of how SVD is calculated, the sign of its singular vectors is arbitrary.
zscore (Lee et al. 2008). The z-score method standardizes expression profiles over the samples and then, for each gene set, combines the standardized values as follows. Given a gene set \(\gamma=\{1,\dots,k\}\) with standardized values \(z_1,\dots,z_k\) for each gene in a specific sample, the combined z-score \(Z_\gamma\) for the gene set \(\gamma\) is defined as: \[ Z_\gamma = \frac{\sum_{i=1}^k z_i}{\sqrt{k}}\,. \]
ssgsea (Barbie et al. 2009). Single sample GSEA (ssGSEA) is a non-parametric method that calculates a gene set enrichment score per sample as the normalized difference in empirical cumulative distribution functions (CDFs) of gene expression ranks inside and outside the gene set. By default, the implementation in the GSVA package follows the last step described in (Barbie et al. 2009, online methods, pg. 2) by which pathway scores are normalized, dividing them by the range of calculated values. This normalization step may be switched off using the argument ssgsea.norm in the call to the gsva() function; see below.
gsva (Hänzelmann, Castelo, and Guinney 2013). This is the default method of the package and similarly to ssGSEA, is a non-parametric method that uses the empirical CDFs of gene expression ranks inside and outside the gene set, but it starts by calculating an expression-level statistic that brings gene expression profiles with different dynamic ranges to a common scale.

The interested user may find full technical details about how these methods work in their corresponding articles cited above. If you use any of them in a publication, please cite them with the given bibliographic reference.

3 Overview of the GSVA functionality

The workhorse of the GSVA package is the function gsva(), which takes a parameter object as its main input. There are four classes of parameter objects corresponding to the methods listed above, and may have different additional parameters to tune, but all of them require at least the following two input arguments:

A normalized gene expression dataset, which can be provided in one of the following containers:
- A matrix of expression values with genes corresponding to rows and samples corresponding to columns.
- An ExpressionSet object; see package Biobase.
- A SummarizedExperiment object, see package SummarizedExperiment.
A collection of gene sets; which can be provided in one of the following containers:
- A list object where each element corresponds to a gene set defined by a vector of gene identifiers, and the element names correspond to the names of the gene sets.
- A GeneSetCollection object; see package GSEABase.

One advantage of providing the input data using specialized containers such as ExpressionSet, SummarizedExperiment and GeneSetCollection is that the gsva() function will automatically map the gene identifiers between the expression data and the gene sets (internally calling the function mapIdentifiers() from the package GSEABase), when they come from different standard nomenclatures, i.e., Ensembl versus Entrez, provided the input objects contain the appropriate metadata; see next section.

If either the input gene expression data is provided as a matrix object or the gene sets are provided in a list object, or both, it is then the responsibility of the user to ensure that both objects contain gene identifiers following the same standard nomenclature.

Before the actual calculations take place, the gsva() function will apply the following filters:

Discard genes in the input expression data matrix with constant expression.
Discard genes in the input gene sets that do not map to a gene in the input gene expression data matrix.
Discard gene sets that, after applying the previous filters, do not meet a minimum and maximum size, which by default is one for the minimum size and has no limit for the maximum size.

If, as a result of applying these three filters, either no genes or gene sets are left, the gsva() function will prompt an error. A common cause for such an error at this stage is that gene identifiers between the expression data matrix and the gene sets do not belong to the same standard nomenclature and could not be mapped. This may happen because either the input data were not provided using some of the specialized containers described above or the necessary metadata in those containers that allows the software to successfully map gene identifiers, is missing.

The method employed by the gsva() function is determined by the class of the parameter object that it receives as an input. An object constructed using the gsvaParam() function runs the method described by Hänzelmann, Castelo, and Guinney (2013), but this can be changed using the parameter constructor functions plageParam(), zscoreParam(), or ssgseaParam(), corresponding to the methods briefly described in the introduction; see also their corresponding help pages.

When using gsvaParam(), the user can additionally tune the following parameters:

kcdf: The first step of the GSVA algorithm brings gene expression profiles to a common scale by calculating an expression statistic through a non-parametric estimation of the CDF across samples. Such a non-parametric estimation employs a kernel function and the kcdf parameter allows the user to specify three possible values for that function: (1) "Gaussian", the default value, which is suitable for continuous expression data, such as microarray fluorescent units in logarithmic scale and RNA-seq log-CPMs, log-RPKMs or log-TPMs units of expression; (2) "Poisson", which is suitable for integer counts, such as those derived from RNA-seq alignments; (3) "none", which will enforce a direct estimation of the CDF without a kernel function.
maxDiff: The last step of the GSVA algorithm calculates the gene set enrichment score from two Kolmogorov-Smirnov random walk statistics. This parameter is a logical flag that allows the user to specify two possible ways to do such calculation: (1) TRUE, the default value, where the enrichment score is calculated as the magnitude difference between the largest positive and negative random walk deviations; (2) FALSE, where the enrichment score is calculated as the maximum distance of the random walk from zero.
absRanking: Logical flag used only when maxDiff=TRUE. By default, absRanking=FALSE and it implies that a modified Kuiper statistic is used to calculate enrichment scores, taking the magnitude difference between the largest positive and negative random walk deviations. When absRanking=TRUE the original Kuiper statistic is used, by which the largest positive and negative random walk deviations are added together. In this case, gene sets with genes enriched on either extreme (high or low) will be regarded as highly activated.
tau: Exponent defining the weight of the tail in the random walk. By default tau=1.

In general, the default values for the previous parameters are suitable for most analysis settings, which usually consist of some kind of normalized continuous expression values.

4 Gene set definitions

Gene sets constitute a simple, yet useful, way to define pathways because we use pathway membership definitions only, neglecting the information on molecular interactions. Gene set definitions are a crucial input to any gene set enrichment analysis because if our gene sets do not capture the biological processes we are studying, we will likely not find any relevant insights in our data from an analysis based on these gene sets.

There are multiple sources of gene sets, the most popular ones being The Gene Ontology (GO) project and The Molecular Signatures Database (MSigDB). Sometimes gene set databases will not include the ones we need. In such a case we should either curate our own gene sets or use techniques to infer them from data.

The most basic data container for gene sets in R is the list class of objects, as illustrated before in the quick start section, where we defined a toy collection of three gene sets stored in a list object called gs:

class(gs)
[1] "list"
length(gs)
[1] 100
head(lapply(gs, head))
$gs1
[1] "g1251" "g8931" "g5022" "g6502" "g6803" "g4423"

$gs2
[1] "g2661" "g8652" "g6236" "g6448" "g9065" "g5304"

$gs3
[1] "g7595" "g6938" "g7227" "g8239" "g6297" "g5651"

$gs4
[1] "g5151" "g3084" "g986"  "g5803" "g9195" "g8053"

$gs5
[1] "g9091" "g7895" "g6555" "g8073" "g7714" "g9075"

$gs6
[1] "g7460" "g9664" "g7831" "g4350" "g725"  "g8709"

Using a Bioconductor organism-level package such as org.Hs.eg.db we can easily build a list object containing a collection of gene sets defined as GO terms with annotated Entrez gene identifiers, as follows:

library(org.Hs.eg.db)

goannot <- select(org.Hs.eg.db, keys=keys(org.Hs.eg.db), columns="GO")
head(goannot)
  ENTREZID         GO EVIDENCE ONTOLOGY
1        1 GO:0003674       ND       MF
2        1 GO:0005576      HDA       CC
3        1 GO:0005576      IDA       CC
4        1 GO:0005576      TAS       CC
5        1 GO:0005615      HDA       CC
6        1 GO:0005886      IBA       CC
genesbygo <- split(goannot$ENTREZID, goannot$GO)
length(genesbygo)
[1] 18809
head(genesbygo)
$`GO:0000002`
 [1] "291"   "1890"  "4205"  "4358"  "4976"  "9361"  "10000" "55186" "55186"
[10] "80119" "84275" "84275" "92667"

$`GO:0000003`
[1] "2796"   "2797"   "8510"   "286826"

$`GO:0000009`
[1] "55650" "79087"

$`GO:0000010`
[1] "23590" "57107"

$`GO:0000012`
 [1] "1161"      "2074"      "3981"      "7141"      "7515"      "23411"    
 [7] "54840"     "54840"     "54840"     "55775"     "55775"     "200558"   
[13] "100133315"

$`GO:0000014`
 [1] "2021"  "2067"  "2072"  "4361"  "4361"  "5932"  "6419"  "6419"  "9941" 
[10] "10111" "64421"

A more sophisticated container for gene sets is the GeneSetCollection object class defined in the GSEABase package, which also provides the function getGmt() to import gene matrix transposed (GMT) files such as those provided by MSigDB into a GeneSetCollection object. The experiment data package GSVAdata provides one such object with the old (3.0) version of the C2 collection of curated genesets from MSigDB, which can be loaded as follows.

library(GSEABase)
library(GSVAdata)

data(c2BroadSets)
class(c2BroadSets)
[1] "GeneSetCollection"
attr(,"package")
[1] "GSEABase"
c2BroadSets
GeneSetCollection
  names: NAKAMURA_CANCER_MICROENVIRONMENT_UP, NAKAMURA_CANCER_MICROENVIRONMENT_DN, ..., ST_PHOSPHOINOSITIDE_3_KINASE_PATHWAY (3272 total)
  unique identifiers: 5167, 100288400, ..., 57191 (29340 total)
  types in collection:
    geneIdType: EntrezIdentifier (1 total)
    collectionType: BroadCollection (1 total)

The documentation of GSEABase contains a description of the GeneSetCollection class and its associated methods.

5 Quantification of pathway activity in bulk microarray and RNA-seq data

Here we illustrate how GSVA provides an analogous quantification of pathway activity in both microarray and RNA-seq data by using two such datasets that have been derived from the same biological samples. More concretely, we will use gene expression data of lymphoblastoid cell lines (LCL) from HapMap individuals that have been profiled using both technologies (Huang et al. 2007, @pickrell_understanding_2010). These data form part of the experimental package GSVAdata and the corresponding help pages contain details on how the data were processed. We start loading these data and verifying that they indeed contain expression data for the same genes and samples, as follows:

library(Biobase)

data(commonPickrellHuang)

stopifnot(identical(featureNames(huangArrayRMAnoBatchCommon_eset),
                    featureNames(pickrellCountsArgonneCQNcommon_eset)))
stopifnot(identical(sampleNames(huangArrayRMAnoBatchCommon_eset),
                    sampleNames(pickrellCountsArgonneCQNcommon_eset)))

Next, for the current analysis we use the subset of canonical pathways from the C2 collection of MSigDB Gene Sets. These correspond to the following pathways from KEGG, REACTOME and BIOCARTA:

canonicalC2BroadSets <- c2BroadSets[c(grep("^KEGG", names(c2BroadSets)),
                                      grep("^REACTOME", names(c2BroadSets)),
                                      grep("^BIOCARTA", names(c2BroadSets)))]
canonicalC2BroadSets
GeneSetCollection
  names: KEGG_GLYCOLYSIS_GLUCONEOGENESIS, KEGG_CITRATE_CYCLE_TCA_CYCLE, ..., BIOCARTA_ACTINY_PATHWAY (833 total)
  unique identifiers: 55902, 2645, ..., 8544 (6744 total)
  types in collection:
    geneIdType: EntrezIdentifier (1 total)
    collectionType: BroadCollection (1 total)

Additionally, we extend this collection of gene sets with two formed by genes with sex-specific expression, which also form part of the GSVAdata experiment data package. Here we use the constructor function GeneSet from the GSEABase package to build the objects that we add to the GeneSetCollection object canonicalC2BroadSets.

data(genderGenesEntrez)

MSY <- GeneSet(msYgenesEntrez, geneIdType=EntrezIdentifier(),
               collectionType=BroadCollection(category="c2"),
               setName="MSY")
MSY
setName: MSY 
geneIds: 266, 84663, ..., 353513 (total: 34)
geneIdType: EntrezId
collectionType: Broad
  bcCategory: c2 (Curated)
  bcSubCategory: NA
details: use 'details(object)'
XiE <- GeneSet(XiEgenesEntrez, geneIdType=EntrezIdentifier(),
               collectionType=BroadCollection(category="c2"),
               setName="XiE")
XiE
setName: XiE 
geneIds: 293, 8623, ..., 1121 (total: 66)
geneIdType: EntrezId
collectionType: Broad
  bcCategory: c2 (Curated)
  bcSubCategory: NA
details: use 'details(object)'

canonicalC2BroadSets <- GeneSetCollection(c(canonicalC2BroadSets, MSY, XiE))
canonicalC2BroadSets
GeneSetCollection
  names: KEGG_GLYCOLYSIS_GLUCONEOGENESIS, KEGG_CITRATE_CYCLE_TCA_CYCLE, ..., XiE (835 total)
  unique identifiers: 55902, 2645, ..., 1121 (6810 total)
  types in collection:
    geneIdType: EntrezIdentifier (1 total)
    collectionType: BroadCollection (1 total)

We calculate now GSVA enrichment scores for these gene sets using first the normalized microarray data and then the normalized RNA-seq integer count data. Note that the only requirement to do the latter is to set the argument kcdf="Poisson", which is "Gaussian" by default. Note, however, that if our RNA-seq normalized expression levels would be continuous, such as log-CPMs, log-RPKMs or log-TPMs, the default value of the kcdf argument should remain unchanged.

huangPar <- gsvaParam(huangArrayRMAnoBatchCommon_eset, canonicalC2BroadSets,
                      minSize=5, maxSize=500)
esmicro <- gsva(huangPar)
pickrellPar <- gsvaParam(pickrellCountsArgonneCQNcommon_eset,
                         canonicalC2BroadSets, minSize=5, maxSize=500,
                         kcdf="Poisson")
esrnaseq <- gsva(pickrellPar)

We are going to assess how gene expression profiles correlate between microarray and RNA-seq data and compare those correlations with the ones derived at pathway level. To compare gene expression values of both technologies, we will transform first the RNA-seq integer counts into log-CPM units of expression using the cpm() function from the edgeR package.

library(edgeR)

lcpms <- cpm(exprs(pickrellCountsArgonneCQNcommon_eset), log=TRUE)

We calculate Spearman correlations between gene expression profiles of the previous log-CPM values and the microarray RMA values.

genecorrs <- sapply(1:nrow(lcpms),
                    function(i, expmicro, exprnaseq)
                      cor(expmicro[i, ], exprnaseq[i, ], method="spearman"),
                    exprs(huangArrayRMAnoBatchCommon_eset), lcpms)
names(genecorrs) <- rownames(lcpms)

Now calculate Spearman correlations between GSVA enrichment scores derived from the microarray and the RNA-seq data.

pwycorrs <- sapply(1:nrow(esmicro),
                   function(i, esmicro, esrnaseq)
                     cor(esmicro[i, ], esrnaseq[i, ], method="spearman"),
                   exprs(esmicro), exprs(esrnaseq))
names(pwycorrs) <- rownames(esmicro)

Figure 1 below shows the two distributions of these correlations and we can see that GSVA enrichment scores provide an agreement between microarray and RNA-seq data comparable to the one observed between gene-level units of expression.

par(mfrow=c(1, 2), mar=c(4, 5, 3, 2))
hist(genecorrs, xlab="Spearman correlation",
     main="Gene level\n(RNA-seq log-CPMs vs microarray RMA)",
     xlim=c(-1, 1), col="grey", las=1)
hist(pwycorrs, xlab="Spearman correlation",
     main="Pathway level\n(GSVA enrichment scores)",
     xlim=c(-1, 1), col="grey", las=1)

Figure 1: Comparison of correlation values of gene and pathway expression profiles derived from microarray and RNA-seq data

Finally, in Figure 2 we compare the actual GSVA enrichment scores for two gene sets formed by genes with sex-specific expression. Concretely, one gene set (XIE) formed by genes that escape chromosome X-inactivation in females (Carrel and Willard 2005) and another gene set (MSY) formed by genes located on the male-specific region of chromosome Y (Skaletsky et al. 2003).

par(mfrow=c(1, 2))
rmsy <- cor(exprs(esrnaseq)["MSY", ], exprs(esmicro)["MSY", ])
plot(exprs(esrnaseq)["MSY", ], exprs(esmicro)["MSY", ],
     xlab="GSVA scores RNA-seq", ylab="GSVA scores microarray",
     main=sprintf("MSY R=%.2f", rmsy), las=1, type="n")
fit <- lm(exprs(esmicro)["MSY", ] ~ exprs(esrnaseq)["MSY", ])
abline(fit, lwd=2, lty=2, col="grey")
maskPickrellFemale <- pickrellCountsArgonneCQNcommon_eset$Gender == "Female"
maskHuangFemale <- huangArrayRMAnoBatchCommon_eset$Gender == "Female"
points(exprs(esrnaseq["MSY", maskPickrellFemale]),
       exprs(esmicro)["MSY", maskHuangFemale],
       col="red", pch=21, bg="red", cex=1)
maskPickrellMale <- pickrellCountsArgonneCQNcommon_eset$Gender == "Male"
maskHuangMale <- huangArrayRMAnoBatchCommon_eset$Gender == "Male"
points(exprs(esrnaseq)["MSY", maskPickrellMale],
       exprs(esmicro)["MSY", maskHuangMale],
       col="blue", pch=21, bg="blue", cex=1)
legend("topleft", c("female", "male"), pch=21, col=c("red", "blue"),
       pt.bg=c("red", "blue"), inset=0.01)
rxie <- cor(exprs(esrnaseq)["XiE", ], exprs(esmicro)["XiE", ])
plot(exprs(esrnaseq)["XiE", ], exprs(esmicro)["XiE", ],
     xlab="GSVA scores RNA-seq", ylab="GSVA scores microarray",
     main=sprintf("XiE R=%.2f", rxie), las=1, type="n")
fit <- lm(exprs(esmicro)["XiE", ] ~ exprs(esrnaseq)["XiE", ])
abline(fit, lwd=2, lty=2, col="grey")
points(exprs(esrnaseq["XiE", maskPickrellFemale]),
       exprs(esmicro)["XiE", maskHuangFemale],
       col="red", pch=21, bg="red", cex=1)
points(exprs(esrnaseq)["XiE", maskPickrellMale],
       exprs(esmicro)["XiE", maskHuangMale],
       col="blue", pch=21, bg="blue", cex=1)
legend("topleft", c("female", "male"), pch=21, col=c("red", "blue"),
       pt.bg=c("red", "blue"), inset=0.01)

Comparison of GSVA enrichment scores obtained from microarray and RNA-seq data for two gene sets formed by genes with sex-specific expression.

Figure 2: Comparison of GSVA enrichment scores obtained from microarray and RNA-seq data for two gene sets formed by genes with sex-specific expression

We can see how microarray and RNA-seq single-sample GSVA enrichment scores correlate very well in these gene sets, with \(\rho=0.80\) for the male-specific gene set and \(\rho=0.79\) for the female-specific gene set. Male and female samples show higher GSVA enrichment scores in their corresponding gene set.

6 Example applications

6.1 Molecular signature identification

In (Verhaak et al. 2010) four subtypes of glioblastoma multiforme (GBM) -proneural, classical, neural and mesenchymal- were identified by the characterization of distinct gene-level expression patterns. Using four gene set signatures specific to brain cell types (astrocytes, oligodendrocytes, neurons and cultured astroglial cells), derived from murine models by Cahoy et al. (2008), we replicate the analysis of Verhaak et al. (2010) by using GSVA to transform the gene expression measurements into enrichment scores for these four gene sets, without taking the sample subtype grouping into account. We start by having a quick glance to the data, which forms part of the GSVAdata package:

data(gbm_VerhaakEtAl)
gbm_eset
ExpressionSet (storageMode: lockedEnvironment)
assayData: 11861 features, 173 samples 
  element names: exprs 
protocolData: none
phenoData
  rowNames: TCGA.02.0003.01A.01 TCGA.02.0010.01A.01 ...
    TCGA.12.0620.01A.01 (173 total)
  varLabels: subtype
  varMetadata: labelDescription channel
featureData: none
experimentData: use 'experimentData(object)'
Annotation:  
head(featureNames(gbm_eset))
[1] "AACS"    "FSTL1"   "ELMO2"   "CREB3L1" "RPS11"   "PNMA1"  
table(gbm_eset$subtype)

  Classical Mesenchymal      Neural   Proneural 
         38          56          26          53 
data(brainTxDbSets)
lengths(brainTxDbSets)
      astrocytic_up        astroglia_up         neuronal_up oligodendrocytic_up 
                 85                  88                  98                  70 
lapply(brainTxDbSets, head)
$astrocytic_up
[1] "GRHL1"   "GPAM"    "PAPSS2"  "MERTK"   "BTG1"    "SLC46A1"

$astroglia_up
[1] "BST2"     "SERPING1" "ACTA2"    "C9orf167" "C1orf31"  "ANXA4"   

$neuronal_up
[1] "STXBP1"  "JPH4"    "CACNG3"  "BRUNOL6" "CLSTN2"  "FAM123C"

$oligodendrocytic_up
[1] "DCT"    "ZNF536" "GNG8"   "ELOVL6" "NR2C1"  "RCBTB1"

GSVA enrichment scores for the gene sets contained in brainTxDbSets are calculated, in this case using mx.diff=FALSE, as follows:

gbmPar <- gsvaParam(gbm_eset, brainTxDbSets, maxDiff=FALSE)
gbm_es <- gsva(gbmPar)

Figure 3 shows the GSVA enrichment scores obtained for the up-regulated gene sets across the samples of the four GBM subtypes. As expected, the neural class is associated with the neural gene set and the astrocytic gene sets. The mesenchymal subtype is characterized by the expression of mesenchymal and microglial markers, thus we expect it to correlate with the astroglial gene set. The proneural subtype shows high expression of oligodendrocytic development genes, thus it is not surprising that the oligodendrocytic gene set is highly enriched for ths group. Interestingly, the classical group correlates highly with the astrocytic gene set. In summary, the resulting GSVA enrichment scores recapitulate accurately the molecular signatures from Verhaak et al. (2010).

library(RColorBrewer)
subtypeOrder <- c("Proneural", "Neural", "Classical", "Mesenchymal")
sampleOrderBySubtype <- sort(match(gbm_es$subtype, subtypeOrder),
                             index.return=TRUE)$ix
subtypeXtable <- table(gbm_es$subtype)
subtypeColorLegend <- c(Proneural="red", Neural="green",
                        Classical="blue", Mesenchymal="orange")
geneSetOrder <- c("astroglia_up", "astrocytic_up", "neuronal_up",
                  "oligodendrocytic_up")
geneSetLabels <- gsub("_", " ", geneSetOrder)
hmcol <- colorRampPalette(brewer.pal(10, "RdBu"))(256)
hmcol <- hmcol[length(hmcol):1]

heatmap(exprs(gbm_es)[geneSetOrder, sampleOrderBySubtype], Rowv=NA,
        Colv=NA, scale="row", margins=c(3,5), col=hmcol,
        ColSideColors=rep(subtypeColorLegend[subtypeOrder],
                          times=subtypeXtable[subtypeOrder]),
        labCol="", gbm_es$subtype[sampleOrderBySubtype],
        labRow=paste(toupper(substring(geneSetLabels, 1,1)),
                     substring(geneSetLabels, 2), sep=""),
        cexRow=2, main=" \n ")
par(xpd=TRUE)
text(0.23,1.21, "Proneural", col="red", cex=1.2)
text(0.36,1.21, "Neural", col="green", cex=1.2)
text(0.47,1.21, "Classical", col="blue", cex=1.2)
text(0.62,1.21, "Mesenchymal", col="orange", cex=1.2)
mtext("Gene sets", side=4, line=0, cex=1.5)
mtext("Samples          ", side=1, line=4, cex=1.5)

Figure 3: Heatmap of GSVA scores for cell-type brain signatures from murine models (y-axis) across GBM samples grouped by GBM subtype

6.2 Differential expression at pathway level

We illustrate here how to conduct a differential expression analysis at pathway level. We will use an example gene expression microarray data from Armstrong et al. (2002), which consists of 37 different individuals with human acute leukemia, where 20 of them have conventional childhood acute lymphoblastic leukemia (ALL) and the other 17 are affected with the MLL (mixed-lineage leukemia gene) translocation. This leukemia data set is stored as an ExpressionSet object called leukemia in the GSVAdata package and and details on how the data was pre-processed can be found in the corresponding help page. Jointly with the RMA expression values, we provide some metadata including the main phenotype corresponding to the leukemia sample subtype.

data(leukemia)
leukemia_eset
ExpressionSet (storageMode: lockedEnvironment)
assayData: 12626 features, 37 samples 
  element names: exprs 
protocolData
  sampleNames: CL2001011101AA.CEL CL2001011102AA.CEL ...
    CL2001011152AA.CEL (37 total)
  varLabels: ScanDate
  varMetadata: labelDescription
phenoData
  sampleNames: CL2001011101AA.CEL CL2001011102AA.CEL ...
    CL2001011152AA.CEL (37 total)
  varLabels: subtype
  varMetadata: labelDescription channel
featureData: none
experimentData: use 'experimentData(object)'
Annotation: hgu95a

Next, we calculate GSVA enrichment scores using a subset of gene sets from the MSigDB C2 collection that represent signatures of genetic and chemical perturbations (CGP), and setting the the minimum and maximum gene set size to 10 and 500 genes, respectively.

cgpC2BroadSets <- c2BroadSets[c(grep("_UP$", names(c2BroadSets)),
                                grep("_DN$", names(c2BroadSets)))]
cgpC2BroadSets
leukPar <- gsvaParam(leukemia_eset, cgpC2BroadSets,
                     minSize=10, maxSize=500)
leukemia_es <- gsva(leukPar)

The object returned by the function gsva() is always of the same class as the input object with the expression data. Therefore, in this case, we obtain an ExpressionSet object with features corresponding to gene sets.

class(leukemia_es)
[1] "ExpressionSet"
attr(,"package")
[1] "Biobase"
leukemia_es
ExpressionSet (storageMode: lockedEnvironment)
assayData: 1305 features, 37 samples 
  element names: exprs 
protocolData: none
phenoData
  sampleNames: CL2001011101AA.CEL CL2001011102AA.CEL ...
    CL2001011152AA.CEL (37 total)
  varLabels: subtype
  varMetadata: labelDescription channel
featureData: none
experimentData: use 'experimentData(object)'
Annotation:  
head(featureNames(leukemia_es))
[1] "NAKAMURA_CANCER_MICROENVIRONMENT_UP"         
[2] "WEST_ADRENOCORTICAL_TUMOR_MARKERS_UP"        
[3] "WINTER_HYPOXIA_UP"                           
[4] "PYEON_HPV_POSITIVE_TUMORS_UP"                
[5] "NAKAMURA_TUMOR_ZONE_PERIPHERAL_VS_CENTRAL_UP"
[6] "PICCALUGA_ANGIOIMMUNOBLASTIC_LYMPHOMA_UP"

We will perform now a differential expression analysis using limma (Smyth 2004) between the two different leukemia subtypes.

library(limma)

mod <- model.matrix(~ factor(leukemia_es$subtype))
colnames(mod) <- c("ALL", "MLLvsALL")
fit <- lmFit(leukemia_es, mod)
fit <- eBayes(fit)
res <- decideTests(fit, p.value=0.01)
summary(res)
        ALL MLLvsALL
Down      0       21
NotSig 1305     1255
Up        0       29

As Figure 4 below shows, GSVA scores have higher precision for larger gene sets111 Thanks to Gordon Smyth for point this out to us..

gssizes <- lengths(geneIds(cgpC2BroadSets)) ## fetch gene set sizes
mt <- match(rownames(leukemia_es), names(gssizes))
gssizes <- gssizes[mt] ## rearrange gene set sizes to the rows of GSVA scores
plot(sqrt(gssizes), sqrt(fit$sigma), xlab="Sqrt(gene sets sizes)",
     ylab="Sqrt(standard deviation)", las=1, pch=".", cex=3)

Figure 4: Residual standard deviation of GSVA scores as function of gene set size

In such a setting, we can improve the analysis of differentially expressed pathways by using the limma-trend approach (Phipson et al. 2016) setting the trend parameter in the call to the eBayes() function to the vector of gene set sizes, in one-to-one correspondence with the gene sets in the rows of the GSVA scores container, as calculated before in gssizes.

fit <- eBayes(fit, trend=gssizes)
res <- decideTests(fit, p.value=0.01)
summary(res)
        ALL MLLvsALL
Down      0       20
NotSig 1305     1258
Up        0       27

There are 47 MSigDB C2 differentially expressed pathways with FDR < 5%. Figure 5 below shows a volcano plot of the expression changes.

tt <- topTable(fit, coef=2, n=Inf)
DEpwys <- rownames(tt)[tt$adj.P.Val <= 0.01]
plot(tt$logFC, -log10(tt$P.Value), pch=".", cex=4, col=grey(0.75),
     main="", xlab="GSVA enrichment score difference", las=1,
     ylab=expression(-log[10]~~Raw~P-value))
abline(h=-log10(max(tt$P.Value[tt$adj.P.Val <= 0.01])),
       col=grey(0.5), lwd=1, lty=2)
points(tt$logFC[match(DEpwys, rownames(tt))],
       -log10(tt$P.Value[match(DEpwys, rownames(tt))]),
       pch=".", cex=5, col="darkred")
text(max(tt$logFC)*0.85, -log10(max(tt$P.Value[tt$adj.P.Val <= 0.01])),
     "1% FDR", pos=3)

Figure 5: Volcano plot for the differential expression analysis at pathway level between two leukemia subtypes

Figure 6 below shows a heatmap of GSVA enrichment scores for the 47 differentially expressed pathways.

DEpwys_es <- exprs(leukemia_es[DEpwys, ])
colorLegend <- c("darkred", "darkblue")
names(colorLegend) <- c("ALL", "MLL")
sample.color.map <- colorLegend[pData(leukemia_es)[, "subtype"]]
names(sample.color.map) <- colnames(DEpwys_es)
sampleClustering <- hclust(as.dist(1-cor(DEpwys_es, method="spearman")),
                           method="complete")
geneSetClustering <- hclust(as.dist(1-cor(t(DEpwys_es), method="pearson")),
                            method="complete")
heatmap(DEpwys_es, ColSideColors=sample.color.map, xlab="samples",
        ylab="Pathways", margins=c(2, 20),
        labRow=substr(gsub("_", " ", gsub("^KEGG_|^REACTOME_|^BIOCARTA_", "",
                                          rownames(DEpwys_es))), 1, 35),
        labCol="", scale="row", Colv=as.dendrogram(sampleClustering),
        Rowv=as.dendrogram(geneSetClustering))
legend("topleft", names(colorLegend), fill=colorLegend, inset=0.01, bg="white")

Figure 6: Heatmap of GSVA enrichment scores for the differentially expressed pathways between two leukemia subtypes

7 Interactive web app

The gsva() function can be also used through an interactive web app developed with shiny. To start it just type on the R console:

res <- igsva()

It will open your browser with the web app shown here below. The button SAVE & CLOSE will close the app and return the resulting object on the R console. Hence, the need to call igsva() on the right-hand side of an assignment if you want to store the result in your workspace. Alternatively, you can use the DOWNLOAD button to download the result in a CSV file.

In the starting window of the web app, after running GSVA, a non-parametric kernel density estimation of sample profiles of GSVA scores will be shown. By clicking on one of the lines, the cumulative distribution of GSVA scores for the corresponding samples will be shown in the GeneSets tab, as illustrated in the image below.

8 Contributing

GSVA has benefited from contributions by multiple developers, see https://github.com/rcastelo/GSVA/graphs/contributors for a list of them. Contributions to the software codebase of GSVA are welcome as long as contributors abide to the terms of the Bioconductor Contributor Code of Conduct. If you want to contribute to the development of GSVA please open an issue to start discussing your suggestion or, in case of a bugfix or a straightforward feature, directly a pull request.

Session information

Here is the output of sessionInfo() on the system on which this document was compiled running pandoc 2.7.3:

sessionInfo()
R version 4.3.3 (2024-02-29 ucrt)
Platform: x86_64-w64-mingw32/x64 (64-bit)
Running under: Windows Server 2022 x64 (build 20348)

Matrix products: default


locale:
[1] LC_COLLATE=C                          
[2] LC_CTYPE=English_United States.utf8   
[3] LC_MONETARY=English_United States.utf8
[4] LC_NUMERIC=C                          
[5] LC_TIME=English_United States.utf8    

time zone: America/New_York
tzcode source: internal

attached base packages:
[1] stats4    stats     graphics  grDevices utils     datasets  methods  
[8] base     

other attached packages:
 [1] RColorBrewer_1.1-3   edgeR_4.0.16         limma_3.58.1        
 [4] GSVAdata_1.38.0      hgu95a.db_3.13.0     GSEABase_1.64.0     
 [7] graph_1.80.0         annotate_1.80.0      XML_3.99-0.16.1     
[10] org.Hs.eg.db_3.18.0  AnnotationDbi_1.64.1 IRanges_2.36.0      
[13] S4Vectors_0.40.2     Biobase_2.62.0       BiocGenerics_0.48.1 
[16] GSVA_1.50.5          BiocStyle_2.30.0    

loaded via a namespace (and not attached):
 [1] blob_1.2.4                  Biostrings_2.70.3          
 [3] bitops_1.0-7                fastmap_1.1.1              
 [5] SingleCellExperiment_1.24.0 RCurl_1.98-1.14            
 [7] digest_0.6.35               rsvd_1.0.5                 
 [9] lifecycle_1.0.4             statmod_1.5.0              
[11] KEGGREST_1.42.0             RSQLite_2.3.6              
[13] magrittr_2.0.3              compiler_4.3.3             
[15] rlang_1.1.3                 sass_0.4.9                 
[17] tools_4.3.3                 yaml_2.3.8                 
[19] knitr_1.46                  S4Arrays_1.2.1             
[21] bit_4.0.5                   DelayedArray_0.28.0        
[23] abind_1.4-5                 BiocParallel_1.36.0        
[25] HDF5Array_1.30.1            grid_4.3.3                 
[27] beachmat_2.18.1             xtable_1.8-4               
[29] Rhdf5lib_1.24.2             tinytex_0.50               
[31] SummarizedExperiment_1.32.0 cli_3.6.2                  
[33] rmarkdown_2.26              crayon_1.5.2               
[35] httr_1.4.7                  DelayedMatrixStats_1.24.0  
[37] DBI_1.2.2                   cachem_1.0.8               
[39] rhdf5_2.46.1                splines_4.3.3              
[41] zlibbioc_1.48.2             parallel_4.3.3             
[43] BiocManager_1.30.22         XVector_0.42.0             
[45] matrixStats_1.3.0           vctrs_0.6.5                
[47] Matrix_1.6-5                jsonlite_1.8.8             
[49] bookdown_0.39               BiocSingular_1.18.0        
[51] bit64_4.0.5                 irlba_2.3.5.1              
[53] magick_2.8.3                locfit_1.5-9.9             
[55] jquerylib_0.1.4             codetools_0.2-20           
[57] GenomeInfoDb_1.38.8         GenomicRanges_1.54.1       
[59] ScaledMatrix_1.10.0         htmltools_0.5.8.1          
[61] rhdf5filters_1.14.1         GenomeInfoDbData_1.2.11    
[63] R6_2.5.1                    sparseMatrixStats_1.14.0   
[65] evaluate_0.23               lattice_0.22-6             
[67] highr_0.10                  png_0.1-8                  
[69] memoise_2.0.1               bslib_0.7.0                
[71] Rcpp_1.0.12                 SparseArray_1.2.4          
[73] xfun_0.43                   MatrixGenerics_1.14.0      
[75] pkgconfig_2.0.3

References

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Barbie, David A., Pablo Tamayo, Jesse S. Boehm, So Young Kim, Susan E. Moody, Ian F. Dunn, Anna C. Schinzel, et al. 2009. “Systematic RNA Interference Reveals That Oncogenic KRAS-driven Cancers Require TBK1.” Nature 462 (7269): 108–12. https://doi.org/10.1038/nature08460.

Cahoy, John D., Ben Emery, Amit Kaushal, Lynette C. Foo, Jennifer L. Zamanian, Karen S. Christopherson, Yi Xing, et al. 2008. “A Transcriptome Database for Astrocytes, Neurons, and Oligodendrocytes: A New Resource for Understanding Brain Development and Function.” J. Neurosci. 28 (1): 264–78. https://doi.org/10.1523/JNEUROSCI.4178-07.2008.

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Huang, R Stephanie, Shiwei Duan, Wasim K Bleibel, Emily O Kistner, Wei Zhang, Tyson A Clark, Tina X Chen, et al. 2007. “A Genome-Wide Approach to Identify Genetic Variants That Contribute to Etoposide-Induced Cytotoxicity.” Proceedings of the National Academy of Sciences of the United States of America 104 (23): 9758–63.

Lee, Eunjung, Han-Yu Chuang, Jong-Won Kim, Trey Ideker, and Doheon Lee. 2008. “Inferring Pathway Activity Toward Precise Disease Classification.” PLOS Comput Biol 4 (11): e1000217. https://doi.org/10.1371/journal.pcbi.1000217.

Phipson, Belinda, Stanley Lee, Ian J Majewski, Warren S Alexander, and Gordon K Smyth. 2016. “Robust Hyperparameter Estimation Protects Against Hypervariable Genes and Improves Power to Detect Differential Expression.” The Annals of Applied Statistics 10 (2): 946. https://doi.org/10.1214/16-AOAS920.

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Skaletsky, Helen, Tomoko Kuroda-Kawaguchi, Patrick J. Minx, Holland S. Cordum, LaDeana Hillier, Laura G. Brown, Sjoerd Repping, et al. 2003. “The Male-Specific Region of the Human Y Chromosome Is a Mosaic of Discrete Sequence Classes.” Nature 423 (6942): 825–37.

Smyth, Gordon K. 2004. “Linear Models and Empirical Bayes Methods for Assessing Differential Expression in Microarray Experiments.” Stat Appl Genet Mol Biol 3: Article3. https://doi.org/10.2202/1544-6115.1027.

Tomfohr, John, Jun Lu, and Thomas B Kepler. 2005. “Pathway Level Analysis of Gene Expression Using Singular Value Decomposition.” BMC Bioinformatics 6 (September): 225. https://doi.org/10.1186/1471-2105-6-225.

Verhaak, Roel G W, Katherine A Hoadley, Elizabeth Purdom, Victoria Wang, Yuan Qi, Matthew D Wilkerson, C Ryan Miller, et al. 2010. “Integrated Genomic Analysis Identifies Clinically Relevant Subtypes of Glioblastoma Characterized by Abnormalities in PDGFRA, IDH1, EGFR, and NF1.” Cancer Cell 17 (1): 98–110. https://doi.org/10.1016/j.ccr.2009.12.020.