Quickstart
In this section we give a quick introduction to the package and the RSEC wrapper which creates the clustering. We will also demonstrate how to find features (biomarkers) that go along with the clusters.
The Data
We will make use of a single cell RNA sequencing experiment made available in the scRNAseq package.
set.seed(14456) ## for reproducibility, just in case
library(scRNAseq)
fluidigm <- ReprocessedFluidigmData()
We will use the fluidigm dataset (see help("fluidigm")). This dataset is stored as a SummarizedExperiment object. We can access the data with assay and metadata on the samples with colData.
assay(fluidigm)[1:5,1:10]
## SRR1275356 SRR1274090 SRR1275251 SRR1275287 SRR1275364 SRR1275269
## A1BG 0 0 0 0 0 0
## A1BG-AS1 0 0 0 0 0 0
## A1CF 0 0 0 0 0 0
## A2M 0 0 0 31 0 46
## A2M-AS1 0 0 0 0 0 0
## SRR1275263 SRR1275242 SRR1275338 SRR1274117
## A1BG 0 0 0 0
## A1BG-AS1 0 0 0 0
## A1CF 0 0 0 0
## A2M 0 0 0 29
## A2M-AS1 0 0 0 133
colData(fluidigm)[,1:5]
## DataFrame with 130 rows and 5 columns
## NREADS NALIGNED RALIGN TOTAL_DUP PRIMER
## <numeric> <numeric> <numeric> <numeric> <numeric>
## SRR1275356 10554900 7555880 71.5862 58.4931 0.0217638
## SRR1274090 196162 182494 93.0323 14.5122 0.0366826
## SRR1275251 8524470 5858130 68.7213 65.0428 0.0351827
## SRR1275287 7229920 5891540 81.4884 49.7609 0.0208685
## SRR1275364 5403640 4482910 82.9609 66.5788 0.0298284
## ... ... ... ... ... ...
## SRR1275259 5949930 4181040 70.2705 52.5975 0.0205253
## SRR1275253 10319900 7458710 72.2747 54.9637 0.0205342
## SRR1275285 5300270 4276650 80.6873 41.6394 0.0227383
## SRR1275366 7701320 6373600 82.76 68.9431 0.0266275
## SRR1275261 13425000 9554960 71.1727 62.0001 0.0200522
NCOL(fluidigm) #number of samples
## [1] 130
Filtering and normalization
While there are 130 samples, there are only 65 cells, because each cell is sequenced twice at different sequencing depth. We will limit the analysis to the samples corresponding to high sequencing depth.
se <- fluidigm[,colData(fluidigm)[,"Coverage_Type"]=="High"]
We also filter out lowly expressed genes: we retain only those genes with at least 10 reads in at least 10 cells.
wh_zero <- which(rowSums(assay(se))==0)
pass_filter <- apply(assay(se), 1, function(x) length(x[x >= 10]) >= 10)
se <- se[pass_filter,]
dim(se)
## [1] 7069 65
This removed 19186 genes out of 26255. We now have 7069 genes (or features) remaining. Notice that it is important to remove genes with zero counts in all samples (we had 9673 genes which were zero in all samples here). Otherwise, PCA dimensionality reductions and other implementations may have a problem.
Normalization is an important step in any RNA-seq data analysis and many different normalization methods have been proposed in the literature. Comparing normalization methods or finding the best performing normalization in this dataset is outside of the scope of this vignette. Instead, we will use a simple quantile normalization that will at least make our clustering reflect the biology rather than the difference in sequencing depth among the different samples.
fq <- round(limma::normalizeQuantiles(assay(se)))
assays(se) <- list(normalized_counts=fq)
As one last step, we are going to change the name of the columns “Cluster1” and “Cluster2” that some in the dataset and refer to published clustering results from the paper; we will use the terms “Published1” and “Published2” to better distinguish them in later plots from other clustering we will do.
wh<-which(colnames(colData(se)) %in% c("Cluster1","Cluster2"))
colnames(colData(se))[wh]<-c("Published1","Published2")
Clustering with RSEC
We will now run RSEC to find clusters of the cells using the default settings. We set isCount=TRUE to indicate that the data in se is count data, so that the log-transform and other count methods should be applied. We also choose the number of cores on which we want to run the operation in parallel via the parameter ncores. This is a relatively small number of samples, compared to most single-cell sequencing experiments, so we choose cluster on the top 10 PCAs of the data by setting reduceMethod="PCA" and nReducedDims=10 (the default is 50). Finally, we set the minimum cluster size in our ensemble clustering to be 3 cells (consensusMinSize=3). We do this not for biological reasons, but for instructional purposes to allow us to get a larger number of clusters.
Because this procedure is slightly computationally intensive, depending on the user’s machine, we have set this code to not run so that the vignette will compile quickly upon installation. However, it doesn’t take very long (roughly 1-2 minutes) so we recommend users try it themselves. The following code is the example of a common run of RSEC:
library(clusterExperiment)
system.time(rsecFluidigm<-RSEC(se, isCount = TRUE,
reduceMethod="PCA", nReducedDims=10,
ncores=1, random.seed=176201))
However, to exactly replicate the results here, we will set a large number of parameters to make sure that the vignette is back-compatible in case some defaults change. We will explain these parameters as we go along, but many of these parameters are the default.
library(clusterExperiment)
system.time(rsecFluidigm<-RSEC(se,
isCount = TRUE,
k0s = 4:15,
alphas=c(0.1, 0.2, 0.3),
betas = 0.9,
reduceMethod="PCA",
nReducedDims=10,
minSizes=1,
clusterFunction="hierarchical01",
consensusMinSize=3,
consensusProportion=0.7,
dendroReduce= "mad",
dendroNDims=1000,
mergeMethod="adjP",
mergeDEMethod="limma",
mergeCutoff=0.01,
ncores=1,
random.seed=176201))
Instead we have saved the results from this call as a data object in the package and will use the following code to load it into the vignette:
#don't call this routine if you ran the above code.
#it will overwrite the rsecFluidigm you made
library(clusterExperiment)
data("rsecFluidigm")
metadata(rsecFluidigm)$packageVersion
## [1] '2.1.5.9008'
The output
We can look at the object that was created.
rsecFluidigm
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: mad_makeConsensus
## -----------
## Primary cluster type: mergeClusters
## Primary cluster label: mergeClusters
## Table of clusters (of primary clustering):
## -1 m01 m02 m03 m04 m05 m06
## 13 15 17 10 4 3 3
## Total number of clusterings: 38
## Dendrogram run on 'makeConsensus' (cluster index: 2)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? Yes
The print out tells us about the clustering(s) that were created (namely 38 clusterings) and which steps of the workflow have been called (all of them have because we used the wrapper RSEC that does the whole thing). Recall from our brief description above that RSEC clusters the data many times using different parameters before finding an consensus clustering. All of these intermediate clusterings are saved. Each of these intermediate clusterings used subsampling of the data and sequential clustering of the data to find the clustering, while the different clusterings represent the different parameters that were adjusted.
We can see that rsecFluidigm has a built in (S4) class called a ClusterExperiment object. This is a class built for this package and explained in the section on ClusterExperiment Objects. In the object rsecFluidigm the clusterings are stored along with corresponding information for each clustering. Furthermore, all of the information in the original SummarizedExperiment is retained. The print out also tells us information about the “primaryCluster” of rsecFluidigm. Each ClusterExperiment object has a “primaryCluster”, which is the default cluster that the many functions will use unless specified by the user. We are told that the “primaryCluster” for rsecFluidigm is has the label “mergeClusters” – which is the defaul label given to the last cluster of the RSEC function because the last call of the RSEC function is to mergeClusters.
There are many accessor functions that help you get at the information in a ClusterExperiment object and some of the most relevant are described in the section on ClusterExperiment Objects. (ClusterExperiment objects are S4 objects, and are not lists).
For right now we will only mention the most basic such function that retrieves the actual cluster assignments. The final clustering created by RSEC is saved as the primary clustering of the object.
head(primaryCluster(rsecFluidigm),20)
## [1] -1 -1 2 3 -1 -1 -1 1 1 1 2 2 -1 2 4 6 -1 1 4 -1
tableClusters(rsecFluidigm)
##
## -1 m01 m02 m03 m04 m05 m06
## 13 15 17 10 4 3 3
The clusters are encoded by consecutive integers. Notice that some of the samples are assigned the value of -1. -1 is the value assigned in this package for samples that are not assigned to any cluster. Why certain samples are not clustered depends on the underlying choices of the clustering routine and we won’t get into here until we learn a bit more about RSEC. Another special value is -2 discussed in the section on ClusterExperiment objects
This final result of RSEC is the result of running many clusterings and finding the ensembl consensus between them. All of the these intermediate clusterings are saved in rsecFluidigm object. They can be accessed by the clusterMatrix function, that returns a matrix where the columns are the different clusterings and the rows are samples. We show a subset of this matrix here:
head(clusterMatrix(rsecFluidigm)[,1:4])
## mergeClusters makeConsensus k0=4,alpha=0.1 k0=5,alpha=0.1
## SRR1275356 -1 -1 -1 -1
## SRR1275251 -1 -1 -1 -1
## SRR1275287 2 5 3 3
## SRR1275364 3 3 -1 -1
## SRR1275269 -1 -1 -1 -1
## SRR1275263 -1 -1 -1 -1
The “mergeClusters” clustering is the final clustering from RSEC and matches the primary clustering that we saw above. The “makeConsensus” clustering is the result of the initial ensembl concensus among all of the many clusterings that were run, while “mergeClusters” is the result of merging smaller clusters together that did not show enough signs of differences between clusters. The remaining clusters are the result of changing the parameters, and a couple of such clusterings a shown in the above printout of the cluster matrix.
The column names are the clusterLabels for each clustering and can be accessed (and assigned new values!) via the clusterLabels function.
head(clusterLabels(rsecFluidigm))
## [1] "mergeClusters" "makeConsensus" "k0=4,alpha=0.1" "k0=5,alpha=0.1"
## [5] "k0=6,alpha=0.1" "k0=7,alpha=0.1"
We can see the names of more clusterings, and see that the different parameter values tried in each clustering are saved in the names of the clustering. We can also see the different parameter combinations that went into the consensus clustering by using getClusterManyParams (here only 2 different parameters).
head(getClusterManyParams(rsecFluidigm))
## clusteringIndex k alpha
## k0=4,alpha=0.1 3 4 0.1
## k0=5,alpha=0.1 4 5 0.1
## k0=6,alpha=0.1 5 6 0.1
## k0=7,alpha=0.1 6 7 0.1
## k0=8,alpha=0.1 7 8 0.1
## k0=9,alpha=0.1 8 9 0.1
Visualizing the output
clusterExperiment also provides many ways to visualize the output of RSEC (or any set of clusterings run in clusterExperiment, as we’ll show below).
Visualizing many clusterings
The first such useful visualization is a plot of all of the clusterings together using the plotClusters command. For this visualization, it is useful to change the amount of space on the left of the plot to allow for the labels of the clusterings, so we will reset the mar option in par. We also decrease the axisLine argument that decides the amount of space between the axis and the labels to give more space to the labels (axisLine is passed internally to the line option in axis).
defaultMar<-par("mar")
plotCMar<-c(1.1,8.1,4.1,1.1)
par(mar=plotCMar)
plotClusters(rsecFluidigm,main="Clusters from RSEC", whichClusters="workflow", colData=c("Biological_Condition","Published2"), axisLine=-1)
This plot shows the samples in the columns, and different clusterings on the rows. Each sample is color coded based on its clustering for that row, where the colors have been chosen to try to match up clusters across different clusterings that show large overlap. Moreover, the samples have been ordered so that each subsequent clustering (starting at the top and going down) will try to order the samples to keep the clusters together, without rearranging the clustering blocks of the previous clustering/row.
We also added a colData argument in our call, indicating that we also want to visualize some information about the samples saved in the colData slot (inherited from our original fluidigm object). We chose the columns “Biological_Condition” and “Published2” from colData, which correspond to the original biological condition of the experiment, and the clusters reported in the original paper, respectively. The data from colData (when requested) are always shown at the bottom of the plot.
Notice that some samples are white. This indicates that they have the value -1, meaning they were not clustered. In fact, for many clusterings, there is a large amount of white here. This is likely do to the fact that there are only 65 cells here, and the default parameters of RSEC are better suited for a large number of cells, such as seen in more modern single-cell sequencing experiments. The sequential clustering may be problematic for small numbers of cells.
We can use an alternative version of plotClusters called plotClustersWorkflow that will better emphasize the more final clusterings from the ensemble/concensus step and merging steps (it currently does not allow for showing the colData as well, however – only clustering results).
par(mar=plotCMar)
plotClustersWorkflow(rsecFluidigm)
Barplots & contingency tables
We can examine size distribution of a single clustering with the function plotBarplot. By default, the cluster picked will be the primary cluster.
plotBarplot(rsecFluidigm,main=paste("Distribution of samples of",primaryClusterLabel(rsecFluidigm)))
We can also pick a particular intermediate clustering, say our intial consensus clustering before merging.
plotBarplot(rsecFluidigm,whichClusters=c("makeConsensus" ))
We can also compare two specific clusters with a simple barplot using plotBarplot. Here we compare the “makeConsensus” and the “mergeClusters” clusterings.
plotBarplot(rsecFluidigm,whichClusters=c("mergeClusters" ,"makeConsensus"))
Since “makeConsensus” is a partition of “mergeClusters”, there is perfect subsetting within the clusters of “mergeClusters”.
A related plot is to plot a heatmap of the contingency table between two clusterings provided by plotClustersTable. This function plots a heatmap of the results of tableClusters, optionally converting them to proportions using prop.table function based on the parameter margin. Here, we’ll set margin=1, meaning we will show each row (corresponding to a cluster of the mergeCluster clustering), as a proportion – i.e. the grey scale of the heatmap gives (in percentages) how the samples in that row’s cluster are distributed across the clusters of the other clustering, makeConsensus
plotClustersTable(rsecFluidigm,whichClusters=c("mergeClusters" ,"makeConsensus"), margin=1)
Again, since makeConsensus clusters are all completely contained in mergeClusters, this plot has less information than if we were comparing competing clusterings (e.g. different results from mergingClusters, see below). For example, there is nothing on the off-diagonal. But we can still see about how the smaller makeConsensus make up the mergeClusters.
Another version of this plot is given by choosing plotType="bubble", where now the size of the dot at each pair of clusters corresponds to the absolute size of the overlap, and the color scale is again the percentage overlap.
plotClustersTable(rsecFluidigm,whichClusters=c("mergeClusters" ,"makeConsensus"), margin=1,plotType="bubble")
Co-Clustering
We can also visualize the proportion of times samples were together in the individual clusterings (i.e. before the consensus clustering):
plotCoClustering(rsecFluidigm,whichClusters=c("mergeClusters","makeConsensus"))
Note that this is not the result from any particular subsampling (which was done repeatedly for each clustering, and those many matrices are not stored), but rather the proportion of times across the final results of the clusterings we ran. The initial consensus clustering in makeConsensus was made based on these proportions and a particular cutoff of the required proportion of times the samples needed to be together.
Plot of Hierarchy of Clusters
We can visualize how the initial ensembl cluster in makeConsensus was clustered into a hierarchy and merged to give us the final clustering in mergeClusters:
plotDMar<-c(8.1,1.1,5.1,8.1)
par(mar=plotDMar)
plotDendrogram(rsecFluidigm,whichClusters=c("makeConsensus","mergeClusters"))
As shown in this plot, the individual clusters of the makeConsensus ensembl clustering were hierarchically clustered (hence the note that the dendrogram was made from the makeConsensus clustering), and similar sister clusters were merged if there were not enough gene differences between them.
2D plot of clusters
Finally, we can plot a 2-dimensional representation of the data with PCA and color code the samples to get a sense of how the data cluster.
plotReducedDims(rsecFluidigm)
We can also look at a higher number of dimensions (or different dimensions) by changing the parameter ‘whichDims’.
plotReducedDims(rsecFluidigm,whichDims=c(1:4))
In this case we can see that higher dimensions show us a greater amount of separation between the clusters than in just 2 dimensions.
Rerunning RSEC with different parameters
In the next section, we will describe more about the options we could adjust in RSEC. As an example of a few options, we might, for example, want to change the proportion of co-clustering we required in making our makeConsensus
clustering (which used the default of 0.7), or change the proportion of genes that must show differences in order to not merge clusters or the method of deciding. We can call RSEC again on our object rsecFluidigm and it will not redo the many individual clustering steps which are time intensive (unless we request it to rerun it by including the argument rerunClusterMany=TRUE). We demonstrate this in our next command where we change these choices in the following ways:
- set the proportion of co-clustering required by the argument
consensusProportion=0.6,
- make the merge cutoff
mergeCutoff=0.01
- decide to use a different method of estimating the proportion differential for merge by setting
mergeMethod="Storey" instead of the default (“adjP”).
- no longer adjust the minimum cluster size and use the default (
consensusMinSize=5).
These are the main parameters we might frequently want to tweak in RSEC.
rsecFluidigm<-RSEC(rsecFluidigm,isCount=TRUE,consensusProportion=0.6,mergeMethod="JC",mergeCutoff=0.05)
Notice that we save the output over our original object. This is the standard way to work with the ClusterExperiment objects, since the package’s commands just continues to add the clusterings, without deleting anything from before. In this way, we do not duplicate the actual data in our workspace (which is often large).
We can compare the results of our changes with the whichClusters command to explicitly choose the clusterings we want to plot:
defaultMar<-par("mar")
plotCMar<-c(1.1,8.1,4.1,1.1)
par(mar=plotCMar)
plotClusters(rsecFluidigm,main="Clusters from RSEC", whichClusters=c("mergeClusters.1","makeConsensus.1","mergeClusters","makeConsensus"), colData=c("Biological_Condition","Published2"), axisLine=-1)
The clusterings with the .1 appended to the labels are the previous makeConsensus and mergeClusters clusterings from the default setting (see Rerunning to see how different versions are labeled and stored internally). We can see that we lost several clusters with these options.
In what follows, we’ll go back to the original (default) RSEC settings by rerunning RSEC (the original clusters are saved in the rsecFluidigm object, but there is useful information about the merging that is overwritten by our latest call so we will just rerun it to recreate the clustering). Again, we will set a lot of parameters to keep the object the same as before:
rsecFluidigm<-RSEC(rsecFluidigm,
isCount=TRUE,
consensusMinSize=3,
consensusProportion=0.7,
dendroReduce= "mad",
dendroNDims=1000,
mergeMethod="adjP",
mergeCutoff=0.01
)
par(mar=plotCMar)
plotClusters(rsecFluidigm,main="Clusters from RSEC", whichClusters=c("mergeClusters","makeConsensus"), colData=c("Biological_Condition","Published2"), axisLine=-1)
In practice, it can be useful to interactively make choices about these parameters by rerunning each the individual steps of the workflow separately and visualizing the changes before moving to the next step, as we do below during our overview of the steps.
Finding Features related to the clusters
A common practice after determining a set of clusters is to perform differential gene expression analysis in order to find genes that show the greatest differences amongst the clusters. We would stress that this is purely an exploratory technique, and any p-values that result from this analysis are not valid, in the sense that they are likely to be inflated. This is because the same data was used to define the clusters and to perform differential expression analysis.
Since this is a common task, we provide the function getBestFeatures to perform various kinds of differential expression analysis between the clusters. A common F-statistic between groups can be chosen. However, we find that it is far more informative to do pairwise comparisons between clusters, or one cluster against all, in order to find genes that are specific to a particular cluster. An option for all of these choices is provided in the getBestFeatures function.
The getBestFeatures function uses the DE analysis provided by the limma package (Smyth 2004, Ritchie et al. (2015)) or edgeR package (Robinson, Mccarthy, and Smyth 2010). In addition, the getBestFeatures function provides an option to do use the “voom” correction in the limma package (Law et al. 2014) to account for the mean-variance relationship that is common in count data. The tests performed by getBestFeatures are specific contrasts between clustering groups; these contrasts can be retrieved without performing the tests using clusterContrasts, including in a format appropriate for the MAST algorithm.
As mentioned above, there are several types of tests that can be performed to identify features that are different between the clusters which we describe in the section entitled Finding Features related to a Clustering. Here we simply perform all pairwise tests between the clusters.
pairsAllRSEC<-getBestFeatures(rsecFluidigm,contrastType="Pairs",p.value=0.05,
number=nrow(rsecFluidigm),DEMethod="edgeR")
head(pairsAllRSEC)
## IndexInOriginal ContrastName InternalName Contrast Feature logFC
## 1 1465 m01-m02 Cl01-Cl02 Cl01-Cl02 DLK1 15.03569
## 2 3788 m01-m02 Cl01-Cl02 Cl01-Cl02 NNAT -12.95394
## 3 5044 m01-m02 Cl01-Cl02 Cl01-Cl02 RPS4Y1 13.65142
## 4 2291 m01-m02 Cl01-Cl02 Cl01-Cl02 GPC3 13.35216
## 5 4286 m01-m02 Cl01-Cl02 Cl01-Cl02 PLXNA4 -13.74639
## 6 5333 m01-m02 Cl01-Cl02 Cl01-Cl02 SLA -14.39600
## logCPM LR P.Value adj.P.Val
## 1 8.804668 126.60954 2.261671e-29 2.398163e-24
## 2 8.751824 106.60850 5.424014e-25 1.150271e-20
## 3 7.424298 91.39647 1.175859e-21 1.781175e-17
## 4 7.126492 85.56250 2.244924e-20 2.975506e-16
## 5 8.642062 79.38483 5.111709e-19 6.022446e-15
## 6 8.897872 77.52585 1.309969e-18 1.262750e-14
We can visualize only these significantly different pair-wise features with plotHeatmap by using the column “IndexInOriginal” in the result of getBestFeatures to quickly identify the genes to be used in the heatmap. Notice that the same genes can be replicated across different contrasts, so we will not always have unique genes:
length(pairsAllRSEC$Feature)==length(unique(pairsAllRSEC$Feature))
## [1] FALSE
In this case they are not unique because the same gene can be significant for different pairs tests. Hence, we will make sure we take only unique gene values so that they are not plotted multiple times in our heatmap. (This is a good practice even if in a particular case the genes are unique).
plotHeatmap(rsecFluidigm, whichClusters=c("makeConsensus","mergeClusters"),clusterSamplesData="dendrogramValue",
clusterFeaturesData=unique(pairsAllRSEC[,"IndexInOriginal"]),
main="Heatmap of features w/ significant pairwise differences",
breaks=.99)
Notice that the samples clustered into the -1 cluster (i.e. not assigned) are clustered as an outgroup. This is a choice that is made when the dendrogram (described below). These samples can also be mixed into the dendrogram (see makeDendrogram)
We can identify the genes corresponding to the different contrasts with the plotContrastHeatmap function where the genes (rows) are organized by what contrast for which they are significant. The option nBlankLines controls the space between the groups of genes from each contrast. We also give the argument whichCluster="primary" to indicate that the contrasts were created with the primary clustering – this means that the legend will put in the names of the clusters rather than their (internal) numeric id.
plotContrastHeatmap(rsecFluidigm, signif=pairsAllRSEC,nBlankLines=40,whichCluster="primary")
## Warning in sort(as.numeric(internalNames)): NAs introduced by coercion
Overview of the clustering workflow
We give an overview here of the steps used by the RSEC wrapper and more generally in the clusterExperiment package. The section The clustering workflow goes over these steps and the possible arguments in greater details.
The standard clustering workflow steps are the following:
clusterMany – run desired clusteringsmakeConsensus – get a unified clusteringmakeDendrogram – get a hierarchical relationship between the clustersmergeClusters – merge together clusters with little DE between their genes.
These clustering steps are done in one function call by RSEC, described above, which is most straightforward usage. However, to understand the parameters available in RSEC it is useful to go through the steps individually. Furthermore RSEC has streamlined the workflow to concentrate on using the workflow with subsampling and sequential strategies, but going through the individual steps demonstrates how the user can make different choices.
Therefore in this section, we will go through these steps, but instead of using the parameters of RSEC that involve subsampling and are more computationally intensive, we will run through the same steps, only using just basic PAM clustering with no subsampling or sequential clustering. This is simply for the purpose of briefly understanding the intermediate steps that RSEC follows. Later sections will go through these steps in more detail and discuss the particular choices embedded in RSEC.
Step 1: Clustering with clusterMany
clusterMany lets the user quickly pick between many clustering options and run all of the clusterings in one single command. In the quick start we pick a simple set of clusterings based on varying the dimensionality reduction options. The way to designate which options to vary is to give multiple values to an argument.
Here is our call to clusterMany:
ce<-clusterMany(se, clusterFunction="pam",ks=5:10, minSizes=5,
isCount=TRUE,reduceMethod=c("PCA","var"),nFilterDims=c(100,500,1000),
nReducedDims=c(5,15,50),run=TRUE)
In this call to clusterMany we made the follow choices about what to vary:
- set
reduceMethod=c("PCA", "var") meaning run the clustering algorithm trying two different methods for dimensionality reduction: the top principal components and filtering to the top most variable genes
- For PCA reduction, choose 5,15, and 50 principal components for the reduced data set (set
nReducedDims=c(5,15,50))
- For most variable genes reduction, we choose 100, 500, and 1000 most variable genes (set
nFilterDims=c(100,500,1000))
- For the number of clusters, vary from \(k=5,\ldots,10\) (set
ks=5:10)
By giving only a single value to the relative argument, we keep the other possible options fixed, for example:
- we used ‘pam’ for all clustering (
clusterFunction="pam")
- we set
minSizes=5. This is an argument that allows the user to set a minimum required size and clusters of size less than that value will be ignored and samples assigned to them given the unassigned value of -1. The default of 1 would mean that this option is not used.
We also set isCount=TRUE to indicate that our input data are counts. This means that operations for clustering and visualizations will internally transform the data as \(log_2(x+1)\) (We could have alternatively explicitly set a transformation by giving a function to the transFun argument, for example if we wanted \(\sqrt(x)\) or \(log(x+\epsilon)\) or just identity).
We can visualize the resulting clusterings using the plotClusters command as we did for the RSEC results.
defaultMar<-par("mar")
par(mar=plotCMar)
plotClusters(ce,main="Clusters from clusterMany", whichClusters="workflow", colData=c("Biological_Condition","Published2"), axisLine=-1)
ce<-clusterMany(se, clusterFunction="pam",ks=5:10, minSizes=5,
isCount=TRUE,reduceMethod=c("PCA","var"),nFilterDims=c(100,500,1000),
nReducedDims=c(5,15,50),run=TRUE)
test<-getClusterManyParams(ce)
ord<-order(test[,"k"],test[,"nFilterDims"],test[,"nReducedDims"])
plotClusters(ce,main="Clusters from clusterMany", whichClusters=test$clusteringIndex[ord], colData=c("Biological_Condition","Published2"), axisLine=-1)
We can see that some clusters are fairly stable across different choices of dimensions while others can vary dramatically.
Notice that again some samples are white (i.e the value -1, meaning they were not clustered). This is from our choices to require at least 5 samples to make a cluster.
We have set whichClusters="workflow" to only plot clusters created from the workflow. Right now that’s all there are anyway, but as commands get rerun with different options, other clusterings can build up in the object (see discussion in this section about how multiple calls to workflow are stored). So setting whichClusters="workflow" means that we are only going to see our most recent calls to the workflow (so far we only have the 1 step, which is the clusterMany step). We seen already that whichClusters can be set to limit to specific clusterings or specific steps in the workflow .
We cal also give to the whichClusters an argument indices of clusters stored in the ClusterExperiment object, which can allow us to show the clusters in a different order. Here we’ll pick an order which corresponds to varying the number of dimensions, rather than k. We can find the parameters for each clustering using the getClusterManyParams
cmParams<-getClusterManyParams(ce)
head(cmParams)
## clusteringIndex
## reduceMethod=PCA,nReducedDims=5,nFilterDims=NA,k=5 1
## reduceMethod=var,nReducedDims=NA,nFilterDims=100,k=5 2
## reduceMethod=PCA,nReducedDims=15,nFilterDims=NA,k=5 3
## reduceMethod=PCA,nReducedDims=50,nFilterDims=NA,k=5 4
## reduceMethod=var,nReducedDims=NA,nFilterDims=500,k=5 5
## reduceMethod=var,nReducedDims=NA,nFilterDims=1000,k=5 6
## reduceMethod
## reduceMethod=PCA,nReducedDims=5,nFilterDims=NA,k=5 PCA
## reduceMethod=var,nReducedDims=NA,nFilterDims=100,k=5 var
## reduceMethod=PCA,nReducedDims=15,nFilterDims=NA,k=5 PCA
## reduceMethod=PCA,nReducedDims=50,nFilterDims=NA,k=5 PCA
## reduceMethod=var,nReducedDims=NA,nFilterDims=500,k=5 var
## reduceMethod=var,nReducedDims=NA,nFilterDims=1000,k=5 var
## nReducedDims
## reduceMethod=PCA,nReducedDims=5,nFilterDims=NA,k=5 5
## reduceMethod=var,nReducedDims=NA,nFilterDims=100,k=5 NA
## reduceMethod=PCA,nReducedDims=15,nFilterDims=NA,k=5 15
## reduceMethod=PCA,nReducedDims=50,nFilterDims=NA,k=5 50
## reduceMethod=var,nReducedDims=NA,nFilterDims=500,k=5 NA
## reduceMethod=var,nReducedDims=NA,nFilterDims=1000,k=5 NA
## nFilterDims k
## reduceMethod=PCA,nReducedDims=5,nFilterDims=NA,k=5 NA 5
## reduceMethod=var,nReducedDims=NA,nFilterDims=100,k=5 100 5
## reduceMethod=PCA,nReducedDims=15,nFilterDims=NA,k=5 NA 5
## reduceMethod=PCA,nReducedDims=50,nFilterDims=NA,k=5 NA 5
## reduceMethod=var,nReducedDims=NA,nFilterDims=500,k=5 500 5
## reduceMethod=var,nReducedDims=NA,nFilterDims=1000,k=5 1000 5
getClusterManyParams returns the parameter values, as well as the index of the corresponding clustering (i.e. what column it is in the matrix of clusterings). It is important to note that the index will change if we add additional clusterings, as we will do later.
We will set an order with first the PCA, ordered by number of dimensions, then the Var, ordered by number of diminsions
ord<-order(cmParams[,"reduceMethod"],cmParams[,"nReducedDims"])
ind<-cmParams[ord,"clusteringIndex"]
par(mar=plotCMar)
plotClusters(ce,main="Clusters from clusterMany", whichClusters=ind, colData=c("Biological_Condition","Published2"), axisLine=-1)
We see that the order in which the clusters are given to plotClusters changes the plot greatly.
The labels shown are those given automatically by clusterMany but can be a bit much for plotting. We choose to remove “Features” as being too wordy:
clOrig<-clusterLabels(ce)
clOrig<-gsub("Features","",clOrig)
par(mar=plotCMar)
plotClusters(ce,main="Clusters from clusterMany", whichClusters=ind, clusterLabels=clOrig[ind], colData=c("Biological_Condition","Published2"), axisLine=-1)
We could also permanently assign new labels in our ClusterExperiment object if we prefer, for example to be more succinct, by changing the clusterLabels of the object.
There are many different options for how to run plotClusters discussed in in the detailed section on plotClusters, but for now, this plot is good enough for a quick visualization.
Step 2: Find a consensus with makeConsensus
To find a consensus clustering across the many different clusterings created by clusterMany the function makeConsensus can be used next.
ce<-makeConsensus(ce,proportion=1)
The proportion argument indicates the minimum proportion of times samples should be with other samples in the cluster they are assigned to in order to be clustered together in the final assignment. Notice we get a warning that we did not specify any clusters to combine, so it is using the default – those from the clusterMany call.
If we look at the clusterMatrix of the returned ce object, we see that the new cluster from makeConsensus has been added to the existing clusterings. This is the basic strategy of all of these functions in this package. Any clustering function that is applied to an existing ClusterExperiment object adds the new clustering to the set of existing clusterings, so the user does not need to keep track of past clusterings and can easily compare what has changed.
We can again run plotClusters, which will now also show the result of makeConsensus. Instead, we’ll use plotClustersWorkflow which is nicer for looking specifically at the results of makeConsensus
head(clusterMatrix(ce)[,1:3])
## makeConsensus reduceMethod=PCA,nReducedDims=5,nFilterDims=NA,k=5
## SRR1275356 -1 4
## SRR1275251 -1 5
## SRR1275287 -1 1
## SRR1275364 -1 4
## SRR1275269 -1 1
## SRR1275263 -1 5
## reduceMethod=var,nReducedDims=NA,nFilterDims=100,k=5
## SRR1275356 1
## SRR1275251 3
## SRR1275287 4
## SRR1275364 1
## SRR1275269 2
## SRR1275263 1
par(mar=plotCMar)
plotClustersWorkflow(ce)
The choices of proportion=1 in makeConsensus is not usually a great choice, and certainly isn’t helpful here. The clustering from the default makeConsensus leaves most samples unassigned (white in the above plot). This is because we requires samples to be in the same cluster in every clustering in order to be assigned to a cluster together. This is quite stringent. We can vary this by setting the proportion argument to be lower. Explicit details on how makeConsensus makes these clusters are discussed in the section on makeConsensus.
So let’s label the one we found as “makeConsensus,1” and then create a new one. (Making or changing the label to an informative label will make it easier to keep track of this particular clustering later, particularly if we make multiple calls to the workflow).
wh<-which(clusterLabels(ce)=="makeConsensus")
if(length(wh)!=1) stop() else clusterLabels(ce)[wh]<-"makeConsensus,1"
Now we’ll rerun makeConsensus with proportion=0.7. This time, we will give it an informative label upfront in our call to makeConsensus.
ce<-makeConsensus(ce,proportion=0.7,clusterLabel="makeConsensus,0.7")
par(mar=plotCMar)
plotClustersWorkflow(ce)
We see that more clusters are detected. Those that are still not assigned a cluster from makeConsensus clearly vary across the clusterings as to whether the samples are clustered together or not. Varying the proportion argument will adjust whether some of the unclustered samples get added to a cluster. There is also a minSize parameter for makeConsensus, with the default of minSize=5. We could reduce that requirement as well and more of the unclustered samples would be grouped into a cluster. Here, we reduce it to minSize=3 (we’ll call this “makeConsensus,final”). We’ll also choose to show all of the different makeConsensus results in our call to plotClustersWorkflow:
ce<-makeConsensus(ce,proportion=0.7,minSize=3,clusterLabel="makeConsensus,final")
par(mar=plotCMar)
plotClustersWorkflow(ce,whichClusters=c("makeConsensus,final","makeConsensus,0.7","makeConsensus,1"),main="Min. Size=3")
As we did before for RSEC results, we can also visualize the proportion of times these clusters were together across these clusterings (this information was made and stored in the ClusterExperiment object when we called makeConsensus provided that proportion argument is <1):
plotCoClustering(ce)
This visualization can help in determining whether to change the value of proportion (though see makeConsensus for how -1 assignments affect makeConsensus).
Step 3: Merge clusters together with makeDendrogram and mergeClusters
Once you start varying the parameters, is not uncommon in practice to create forty or more clusterings with clusterMany. In which case the results of makeConsensus can often result in too many small clusters. We might wonder if they are necessary or could be logically combined together. We could change the value of proportion in our call to makeConsensus. But we have found that it is often after looking at the clusters, for example with a heatmap, and how different they look on individual genes that we best make this determination, rather than the proportion of times they are together in different clustering routines.
For this reason, we often find the need for an additional clustering step that merges clusters together that are not different, based on running tests of differential expression between the clusters found in makeConsensus. This is done by the function mergeClusters. We often display and use both sets of clusters side-by-side (that from makeConsensus and that from mergeClusters).
mergeClusters needs a hierarchical clustering of the clusters in order to merge clusters; it then goes progressively up that hierarchy, deciding whether two adjacent clusters can be merged. The function makeDendrogram makes such a hierarchy between clusters (by applying hclust to the medoids of the clusters). Because the results of mergeClusters are so dependent on that hierarchy, we require the user to call makeDendrogram rather than calling it automatically internally. This is because different options in makeDendrogram can affect how the clusters are hierarchically ordered, and we want to encourage the user make these choices.
As an example, here we use the 500 most variable genes to make the cluster hierarchy (note we can make different choices here than we did in the clustering).
ce<-makeDendrogram(ce,reduceMethod="var",nDims=500)
plotDendrogram(ce)
Notice that the relative sizes of the clusters are shown as well.
We can see that clusters 1 and 3 are most closely related, at least in the top 500 most variable genes.
Notice I don’t need to make the dendrogram again, because it’s saved in ce.
If we look at the summary of ce, it now has ‘makeDendrogram’ marked as ‘Yes’.
ce
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final
## -----------
## Primary cluster type: makeConsensus
## Primary cluster label: makeConsensus,final
## Table of clusters (of primary clustering):
## -1 c01 c02 c03 c04 c05 c06 c07
## 6 15 14 9 8 5 4 4
## Total number of clusterings: 39
## Dendrogram run on 'makeConsensus,final' (cluster index: 1)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? No
Now we are ready to actually merge clusters together. We run mergeClusters that will go up this hierarchy and compare the level of differential expression (DE) in each pair. In other words, if we focus on the left side of the tree, DE tests are run, between 1 and 3, and between 6 and 8. If there is not enough DE between each of these (based on a cutoff that can be set by the user), then clusters 1 and 3 and/or 6 and 8 will be merged. And so on up the tree.
If the dataset it not too large, is can be useful to first run mergeClusters without actually saving the results so as to preview what the final clustering will be (and perhaps to help in setting the cutoff).
mergeClusters(ce,mergeMethod="adjP",DEMethod="edgeR",plotInfo="mergeMethod")
Notice that unlike our RSEC calls, we have to explicitly choose the DE method that is used in our call to mergeClusters. RSEC chooses the method by default based on the value of isCount argument (but the user can set it in RSEC with mergeDEMethod argument). Since our data is counts, we choose the DE method to be edgeR (which is also what RSEC chooses by default since we set isCount=TRUE).
The default cutoff is cutoff=0.1, meaning those nodes with less than 10% of genes estimated to be differentially expressed between its two children groupings of samples are merged. This is pretty stringent, and as we see it results in no clusterings being kept.
However, the plot tells us the estimate of that proportion for each node. We can decide on a better cutoff using that information. We choose instead cutoff=0.01:
ce<-mergeClusters(ce,mergeMethod="adjP",DEMethod="edgeR",cutoff=0.05)
Notice that now the plot has given the estimates from all of the methods (the default set by plotInfo argument), not just the adjP method. But the dotted lines of the dendrogram indicate the merging performed by the actual choices in merging made in the command (mergeMethod="adjP" and cutoff=0.01).
It can be interesting to visualize the clusterings both with the plotClustersWorkflow and the co-Proportion plot (a heatmap of the proportion of times the samples co-clustered):
par(mar=plotCMar)
plotClustersWorkflow(ce,whichClusters="workflow")
plotCoClustering(ce,whichClusters=c("mergeClusters","makeConsensus"),
colData=c("Biological_Condition","Published2"),annLegend=FALSE)
Notice that mergeClusters combines clusters based on the actual values of the features, while the coClustering plot shows how often the samples clustered together. It is not uncommon that mergeClusters will merge clusters that don’t look “close” on the coClustering plot. This can be due to just the choices of the hierarchical clustering between the clusters, but can also be because the two merged clusters are not often confused for each other across the clustering algorithms, yet still don’t have strong differences on individual genes. This can be the case especially when the clustering is done on reduced PCA space, where an accumulation of small differences might consistently separate the samples (so that comparatively few clusterings are “confused” as to the samples). But because the differences are not strong on individual genes, mergeClusters combines them. These are ultimately different criteria.
Finally, we can do a heatmap visualizing this final step of clustering.
plotHeatmap(ce,clusterSamplesData="dendrogramValue",breaks=.99,
colData=c("Biological_Condition", "Published1", "Published2"))
By choosing “dendrogramValue” for the clustering of the samples, we will be showing the clusters according to the hierarchical ordering of the clusters found by makeDendrogram. The argument breaks=0.99 means that the last color of the heatmap spectrum will be forced to be the top 1% of the data (rather than evenly spaced through the entire range of values). This can be helpful in making sure that rare extreme values in the upper range do not absorb too much space in the color spectrum. There are many more options for plotHeatmap, some of which are discussed in the section on plotHeatmap.
RSEC
The above explanation follows the simple example of PAM. The original RSEC result called RSEC which calls these steps internally. Many of the options described above can be set through a call to RSEC, but some are restricted for simplicity. A detail explanation of the differences can be found in the section RSEC below. But briefly, the following RSEC command, which uses most of the arguments of RSEC:
rsecOut<-RSEC(se, isCount=TRUE, reduceMethod="PCA", nReducedDims=c(50,10), k0s=4:15,
alphas=c(0.1,0.2,0.3),betas=c(0.8,0.9), minSizes=c(1,5), clusterFunction="hierarchical01",
consensusProportion=0.7, consensusMinSize=5,
dendroReduce="mad",dendroNDims=500,
mergeMethod="adjP",mergeCutoff=0.05,
)
would be equivalent to the following individual steps:
ce<-clusterMany(se,ks=4:15,alphas=c(0.1,0.2,0.3),betas=c(0.8,0.9),minSizes=c(1,5),
clusterFunction="hierarchical01", sequential=TRUE,subsample=TRUE,
reduceMethod="PCA",nFilterDims=c(50,10),isCount=TRUE)
ce<-makeConsensus(ce, proportion=0.7, minSize=5)
ce<-makeDendrogram(ce,reduceMethod="mad",nDims=500)
ce<-mergeClusters(ce,mergeMethod="adjP",DEMethod="edgeR",cutoff=0.05,plot=FALSE)
Note that this mean the RSEC function always calls sequential and subsampling.
ClusterExperiment Objects
The ce object that we created by calling clusterMany is a ClusterExperiment object. The ClusterExperiment class is used by this package to keep the data and the clusterings together. It inherits from SingleCellExperiment class (which inherits from SummarizedExperiment) which means the data and colData and other information orginally in the fluidigm object are retained and can be accessed with the same functions as before. The ClusterExperiment object additionally stores clusterings and information about the clusterings along side the data. This helps keep everything together, and like the original SummarizedExperiment object we started with, allows for simple things like subsetting to a reduced set of subjects and being confident that the corresponding clusterings, colData, and so forth are similarly subset.
Typing the name at the control prompt results in a quick summary of the object.
ce
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final
## -----------
## Primary cluster type: mergeClusters
## Primary cluster label: mergeClusters
## Table of clusters (of primary clustering):
## -1 m01 m02 m03 m04
## 6 15 14 13 17
## Total number of clusterings: 40
## Dendrogram run on 'makeConsensus,final' (cluster index: 2)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? Yes
This summary tells us the total number of clusterings (40), and gives some indication as to what parts of the standard workflow have been completed and stored in this object. It also gives information regarding the primaryCluster of the object. The primaryCluster is just one of the clusterings that has been chosen to be the “primary” clustering, meaning that by default various functions will turn to this clustering as the desired clustering to use. clusterMany arbitrarily sets the ‘primaryCluster’ to the first one, and each later step of the workflow sets the primary index to the most recent, but the user can set a specific clustering to be the primaryCluster with primaryClusterIndex. Often, if a function is not given a specific clustering (usually via an option whichCluster or whichClusters) the “primary” cluster is taken by default.
There are also additional commands to access the clusterings and their related information (type help("ClusterExperiment-methods") for more).
The cluster assignments are stored in the clusterMatrix slot of ce, with samples on the rows and different clusterings on the columns. We saw that we can look at the cluster matrix and the primary cluster with the commands clusterMatrix and primaryCluster
head(clusterMatrix(ce))[,1:5]
## mergeClusters makeConsensus,final makeConsensus,0.7
## SRR1275356 -1 -1 -1
## SRR1275251 -1 -1 -1
## SRR1275287 3 6 -1
## SRR1275364 4 4 4
## SRR1275269 3 6 -1
## SRR1275263 4 5 5
## makeConsensus,1
## SRR1275356 -1
## SRR1275251 -1
## SRR1275287 -1
## SRR1275364 -1
## SRR1275269 -1
## SRR1275263 -1
## reduceMethod=PCA,nReducedDims=5,nFilterDims=NA,k=5
## SRR1275356 4
## SRR1275251 5
## SRR1275287 1
## SRR1275364 4
## SRR1275269 1
## SRR1275263 5
primaryCluster(ce)
## [1] -1 -1 3 4 3 4 3 1 1 1 2 2 4 2 3 4 3 1 3 3 2 2 2 1
## [25] -1 1 1 1 4 2 2 4 4 3 3 -1 3 2 -1 4 3 1 1 4 1 1 4 -1
## [49] 3 2 2 2 1 2 3 4 4 1 1 4 4 4 2 4 4
Remember that we made multiple calls to makeConsensus: only the last such call will be shown when we use whichClusters="workflow" in our plotting (see this section for a discussion of how these repeated calls are handled.)
clusterLabels gives the column names of the clusterMatrix; clusterMany has given column names based on the parameter choices, and later steps in the workflow also give a name (or allow the user to set them).
head(clusterLabels(ce),10)
## [1] "mergeClusters"
## [2] "makeConsensus,final"
## [3] "makeConsensus,0.7"
## [4] "makeConsensus,1"
## [5] "reduceMethod=PCA,nReducedDims=5,nFilterDims=NA,k=5"
## [6] "reduceMethod=var,nReducedDims=NA,nFilterDims=100,k=5"
## [7] "reduceMethod=PCA,nReducedDims=15,nFilterDims=NA,k=5"
## [8] "reduceMethod=PCA,nReducedDims=50,nFilterDims=NA,k=5"
## [9] "reduceMethod=var,nReducedDims=NA,nFilterDims=500,k=5"
## [10] "reduceMethod=var,nReducedDims=NA,nFilterDims=1000,k=5"
As we’ve seen, the user can also change these labels.
clusterTypes on the other hand indicates what call made the clustering. Unlike the labels, it is wise to not change the values of clusterTypes unless you are sure of what you are doing because these values are used to identify clusterings from different steps of the workflow.
head(clusterTypes(ce),10)
## [1] "mergeClusters" "makeConsensus" "makeConsensus.2" "makeConsensus.1"
## [5] "clusterMany" "clusterMany" "clusterMany" "clusterMany"
## [9] "clusterMany" "clusterMany"
The information that was in the original fluidigm object has also been preserved, like colData that contains information on each sample.
colData(ce)[,1:5]
## DataFrame with 65 rows and 5 columns
## NREADS NALIGNED RALIGN TOTAL_DUP PRIMER
## <numeric> <numeric> <numeric> <numeric> <numeric>
## SRR1275356 10554900 7555880 71.5862 58.4931 0.0217638
## SRR1275251 8524470 5858130 68.7213 65.0428 0.0351827
## SRR1275287 7229920 5891540 81.4884 49.7609 0.0208685
## SRR1275364 5403640 4482910 82.9609 66.5788 0.0298284
## SRR1275269 10729700 7806230 72.7536 50.4285 0.0204349
## ... ... ... ... ... ...
## SRR1275259 5949930 4181040 70.2705 52.5975 0.0205253
## SRR1275253 10319900 7458710 72.2747 54.9637 0.0205342
## SRR1275285 5300270 4276650 80.6873 41.6394 0.0227383
## SRR1275366 7701320 6373600 82.76 68.9431 0.0266275
## SRR1275261 13425000 9554960 71.1727 62.0001 0.0200522
Another important slot in the ClusterExperiment object is the clusterLegend slot. This consists of a list, one element per column (or clustering) of clusterMatrix, that gives colors and names to each cluster within a clustering.
length(clusterLegend(ce))
## [1] 40
clusterLegend(ce)[1:2]
## $mergeClusters
## clusterIds color name
## [1,] "-1" "white" "-1"
## [2,] "1" "#1F78B4" "m01"
## [3,] "2" "#33A02C" "m02"
## [4,] "3" "#FF7F00" "m03"
## [5,] "4" "#6A3D9A" "m04"
##
## $`makeConsensus,final`
## clusterIds color name
## [1,] "-1" "white" "-1"
## [2,] "1" "#1F78B4" "c01"
## [3,] "2" "#33A02C" "c02"
## [4,] "3" "#FF7F00" "c03"
## [5,] "4" "#6A3D9A" "c04"
## [6,] "5" "#B15928" "c05"
## [7,] "6" "#A6CEE3" "c06"
## [8,] "7" "#bd18ea" "c07"
We can see that each element of clusterLegend consists of a matrix, with number of rows equal to the number of clusters in the clustering. The columns store information about that cluster. clusterIds is the internal id (integer) used in clusterMatrix to identify the cluster, name is a name for the cluster, and color is a color for that cluster. color is used in plotting and visualizing the clusters, and name is an arbitrary character string for a cluster. They are automatically given default values when the ClusterExperiment object is created, but we will see under the description of visualization methods how the user might want to manipulate these for better plotting results.
We can assign new values with a simple assignment operator, but we also provide the functions renameClusters and recolorClusters to help do this. Here we change the internal cluster names of the first clustering from lowercase to uppercase “M” using the function renameClusters:
newName<-gsub("m","M",clusterLegend(ce)[[1]][,"name"])
renameClusters(ce,whichCluster=1,value=newName)
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final
## -----------
## Primary cluster type: mergeClusters
## Primary cluster label: mergeClusters
## Table of clusters (of primary clustering):
## -1 M01 M02 M03 M04
## 6 15 14 13 17
## Total number of clusterings: 40
## Dendrogram run on 'makeConsensus,final' (cluster index: 2)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? Yes
print(ce)
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final
## -----------
## Primary cluster type: mergeClusters
## Primary cluster label: mergeClusters
## Table of clusters (of primary clustering):
## -1 m01 m02 m03 m04
## 6 15 14 13 17
## Total number of clusterings: 40
## Dendrogram run on 'makeConsensus,final' (cluster index: 2)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? Yes
Note that if you choose to not use these functions and instead replace the whole matrix (e.g. clusterLegend(ce)[[1]]<- ...) you should be careful not assign new values to clusterIds column, as the entries must exactly correspond to the internal ids of the clustering stored in the clustering matrix.
Subsetting ClusterExperiment objects
Like SummarizedExperiment or SingleCellExperiment classes, standard subsetting of a ClusterExeriment object will result in a new ClusterExperiment object with all of the relevant parts of the data similarly subsetted.
smallCe<-ce[1:5,1:10]
smallCe
## class: ClusterExperiment
## dim: 5 10
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final
## -----------
## Primary cluster type: mergeClusters
## Primary cluster label: mergeClusters
## Table of clusters (of primary clustering):
## -1 m01 m03 m04
## 2 3 3 2
## Total number of clusterings: 40
## No dendrogram present
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? No
## mergeClusters run? Yes
Notice from looking at the clusterMatrix below that the clustering results have been subset and that after subsetting, the internal cluster ids may change (because they are required to be consecutive).
clusterMatrix(smallCe)[,1:4]
## mergeClusters makeConsensus,final makeConsensus,0.7
## SRR1275356 -1 -1 -1
## SRR1275251 -1 -1 -1
## SRR1275287 2 5 -1
## SRR1275364 3 3 3
## SRR1275269 2 5 -1
## SRR1275263 3 4 4
## SRR1275338 2 2 2
## SRR1274117 1 1 1
## SRR1274089 1 1 1
## SRR1274125 1 1 1
## makeConsensus,1
## SRR1275356 -1
## SRR1275251 -1
## SRR1275287 -1
## SRR1275364 -1
## SRR1275269 -1
## SRR1275263 -1
## SRR1275338 -1
## SRR1274117 1
## SRR1274089 1
## SRR1274125 1
clusterMatrix(ce)[1:10,1:4]
## mergeClusters makeConsensus,final makeConsensus,0.7
## SRR1275356 -1 -1 -1
## SRR1275251 -1 -1 -1
## SRR1275287 3 6 -1
## SRR1275364 4 4 4
## SRR1275269 3 6 -1
## SRR1275263 4 5 5
## SRR1275338 3 3 3
## SRR1274117 1 1 1
## SRR1274089 1 1 1
## SRR1274125 1 1 1
## makeConsensus,1
## SRR1275356 -1
## SRR1275251 -1
## SRR1275287 -1
## SRR1275364 -1
## SRR1275269 -1
## SRR1275263 -1
## SRR1275338 -1
## SRR1274117 1
## SRR1274089 1
## SRR1274125 1
However, the names (and colors) of each cluster should stay the same, which we can see by looking at the clusterLegend information
clusterLegend(smallCe)[["mergeClusters"]]
## clusterIds color name
## [1,] "-1" "white" "-1"
## [2,] "1" "#1F78B4" "m01"
## [3,] "2" "#FF7F00" "m03"
## [4,] "3" "#6A3D9A" "m04"
clusterLegend(ce)[["mergeClusters"]]
## clusterIds color name
## [1,] "-1" "white" "-1"
## [2,] "1" "#1F78B4" "m01"
## [3,] "2" "#33A02C" "m02"
## [4,] "3" "#FF7F00" "m03"
## [5,] "4" "#6A3D9A" "m04"
However subsetting will lose some saved information. In particular, the hierarchy of the clusters that you created with makeDendrogram will be deleted in the new object, as will any saved information about the merging in the mergeClusters step (since that depended on the dendrogram which is now gone).
nodeMergeInfo(ce)
## NodeId Contrast isMerged mergeClusterId Storey
## 1 NodeId1 (X2+X5+X4+X7)/4-(X1+X3+X6)/3 FALSE NA 0.4400905
## 2 NodeId2 X2-(X5+X4+X7)/3 FALSE NA 0.4058566
## 3 NodeId3 X1-(X3+X6)/2 FALSE NA 0.3526666
## 4 NodeId4 X3-X6 TRUE 3 0.2477012
## 5 NodeId5 X5-(X4+X7)/2 TRUE 4 0.4115151
## 6 NodeId6 X4-X7 TRUE NA 0.2295940
## PC adjP locfdr MB JC
## 1 0.3780116 0.12137502 NA 0.4041590 NA
## 2 0.3512809 0.09478003 NA 0.3702080 NA
## 3 0.2905322 0.05658509 NA 0.3131985 NA
## 4 0.1886942 0.01938039 NA 0.2138916 NA
## 5 0.3429098 0.03437544 NA 0.3760079 NA
## 6 0.2254791 0.02447305 NA 0.2837742 NA
nodeMergeInfo(smallCe)
## NULL
The actual clustering created in the mergeClusters step, however, are retained as we’ve seen above.
Another useful type of subsetting can be to subset to only samples contained in a set of particular clusters within a clustering. This can be useful, for example, if you want to visualize the data in only those clusters. The function subsetByCluster allows you to do this, and it returns a new ClusterExperiment object with only those samples. The required input is to identify the values of the clusters you want to keep (by default matching to the clusters’ names)
subCe<-subsetByCluster(ce,whichCluster="mergeClusters",clusterValue=c("m1","m2"))
subCe
## class: ClusterExperiment
## dim: 7069 0
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final
## -----------
## Primary cluster type: mergeClusters
## Primary cluster label: mergeClusters
## Table of clusters (of primary clustering):< table of extent 0 >
## Total number of clusterings: 40
## No dendrogram present
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? No
## mergeClusters run? Yes
The object subCe now can be used for visualizing, or any other analysis.
This kind of subsetting can also be useful in comparing clusterings, where the user might want to subset to all of the samples assigned to Cluster 1 in one clustering and then see what clusters that corresponds to in the other clusterings.
Samples not assigned to a cluster (Negative Valued Cluster Assignments)
The different clusters are stored as consecutive integers, with ‘-1’ and ‘-2’ having special meaning.
Unassigned Samples (-1) ‘-1’ refers to samples that were not clustered by the clustering algorithm. In our example, we removed clusters that didn’t meet specific size criterion, so they were assigned ‘-1’.
Missing from Clustering Run (-2) ‘-2’ is for samples that were not included in the original input to the clustering. This is useful if, for example, you cluster on a subset of the samples, and then want to store this clustering with the clusterings done on all the data. You can create a vector of clusterings that give ‘-2’ to the samples not originally used and then add these clusterings to the ce object manually with addClusters.
We can also wish to go back and assign these samples to the best cluster possible. This can be done with the assignUnassigned function. This function will assign the samples with negative-valued cluster ids to the cluster to which the sample is the closest. Closest is determined by the euclidean distance between an unassigned sample and the median value of the samples assigned to the cluster. The data used by the function to determine the euclidean distances and medians of clusters can be determine by arguments like we see in RSEC and other functions.
ce<-assignUnassigned(ce,whichCluster="mergeClusters",reduceMethod="PCA",nDim=50,makePrimary=FALSE, filterIgnoresUnassigned=TRUE,clusterLabel="mergeClusters_AssignToCluster")
tableClusters(ce,whichCluster="mergeClusters_AssignToCluster")
##
## 1 2 3 4
## 15 15 15 20
Note that we chose makePrimary=FALSE (not the default) so that our original mergeClusters clustering remains the primary one, and doesn’t affect our future calls.
plotClusters(ce,whichCluster=c("mergeClusters_AssignToCluster","mergeClusters"))
You can also create a new object where all of the samples that are not assigned are removed with the removeUnassigned function. This is just a special case of subsetByCluster (above) for the special case of subsetting down to those samples assigned to any cluster.
Dimensionality reduction and SingleCellExperiment Class
There are two varieties of dimensionality reduction supported in clusterExperiment package.
- reducing to a subset of features/genes based on the values of a filter statistic calculated for each gene or
- creation of a smaller number of new features that are functions of the original features, i.e. not a simple selection of existing variables, but rather create new variables to represent the data
For simplicity, we’ll refer to the first as filtering of the data and second as a dimensionality reduction. This is because in the first case, the reduced data set can be quickly recreated by subseting the original data so long as the per-gene statistics have been saved. This means only a single vector of the length of the number of genes needs to be stored for the first type of dimensionality reduction (filtering) while the second kind requires saving a matrix with a value for each observation for each new variable.
ClusterExperiment inherits from the standard Bioconductor SingleCellExperiment class. Briefly, the SingleCellExperiment class extends the SummarizedExperiment class to give a structure for saving the reduced matrices from dimensionality reductions as we described above. They are saved in the slot reducedDims, which is a SimpleList of datasets that have the same number of observations as the original data in the assay slot, but reduced features (?SingleCellExperiment). This gives a unified way to save the results of applying a dimensionality reduction method of the second type; the package also gives helper functions to access them, etc. Multiple such dimensionality reductions can be stored since it is a list, and the user gives them names, e.g. “PCA” or “tSNE”.
ClusterExperiment uses the slot reducedDims to both save the results of dimensionality reductions if they are calculated and and also to reuse them if the necessary ones have already been created. This allows clusterExperiment to make use of any dimensionality reduction method so long as the user saves it in the appropriate slot in a SingleCellExperiment object. The user can also choose like before to have the function (like clusterMany) do the dimensionality reduction (i.e. PCA) internally. The difference is that now the results of the PCA will be stored in the appropriate slot so that they will not need to be recalculated in the future.
We also added in clusterExperiment package a similar procedure for storing the filtering statistics (i.e. statistics calculated on each gene). An example is the the variance across observations, calculated for every gene. clusterExperiment when calculating statistics (like var or mad) will add the per-gene value of the statistic as a column of the rowData of the ClusterExperiment object. Similarly, if the user has already calculated a per-gene statistic and saved it as a column in the rowData slot, this user-defined statistic can be used for filtering. This means that the user is not limited to the built-in filtering functions provided in clusterExperiment.
The functions makeReducedDims and makeFilterStats calculate the dimensionality reduction and filtering statistics, respectively, provided by clusterExperiment and store them in the appropriate slot. To see the current list of built-in functions:
listBuiltInReducedDims()
## [1] "PCA"
listBuiltInFilterStats()
## [1] "var" "abscv" "mad" "mean" "iqr" "median"
The clustering workflow
We will now go into more detail about important options for the main parts of the clustering workflow.
clusterMany
In the quick start section we picked some simple and familiar clustering options that would run quickly and needed little explanation. However, our workflow generally assumes more complex options and more parameter variations are tried. Before getting into the specific options of clusterMany, let us first describe some of these more complicated setups, since many of the arguments of clusterMany depend on understanding them.
Base clustering algorithms and the ClusterFunction class
This package is meant to be able to use and compare different clustering routines. However, the required input, arguments, etc. of different clustering algorithms varies greatly. We create the ClusterFunction class so that we can ensure that the necessary information to fit into our workflow is well defined, and otherwise the other details of the algorithm can be ignored by the workflow. In general, the user will not need to know the details of this class if they want to use the built in functions provided by the package, which can be accessed by character values. To see the set of character values that correspond to built-in functions,
listBuiltInFunctions()
## [1] "pam" "clara" "kmeans" "hierarchical01"
## [5] "hierarchicalK" "tight" "spectral"
If you are interested in implementing your own ClusterFunction object, after reading this section look at our (example)[#customAlgorithm] below.
There are some important features of any clustering algorithm that are encoded in the ClusterFunction object for which it is important to understand because they affect which algorithms can be used when at different parts of the workflow.
algorithmType
We group together algorithms that cluster based on common strategies that affect how we can use them in our workflow. Currently there are two “types” of algorithms we consider, which we call type “K” and “01”. We can determine the type of a builtin function by the following:
algorithmType(c("kmeans","hierarchicalK","hierarchical01"))
## kmeans hierarchicalK hierarchical01
## "K" "K" "01"
The “K” algorithms are so called because their main parameter requirement is that the user specifies the number of clusters (\(K\)) to be created and require an input of k to the clustering function. Built in ‘K’ algorithms are:
listBuiltInTypeK()
## [1] "pam" "clara" "kmeans" "hierarchicalK"
## [5] "spectral"
The “01” algorithms are so named because the algorithm assumes that the input is a disimilarities between samples and that the similarities encoded in \(D\) are on a scale of 0-1. The clustering functions should use this fact to make the primary user-specified parameter be not the number of final clusters, but a measure \(\alpha\) of how dissimilar samples in the same cluster can be (on a scale of 0-1). Given \(\alpha\), the algorithm then implements a method to then determine the clusters (so \(\alpha\) implicitly determines \(K\)). These methods rely on the assumption that because the 0-1 scale has special significance, the user will be able to make an determination more easily as to the level of dissimilarity allowed in a true cluster, rather than predetermine the number of clusters \(K\). The current 01 methods are:
listBuiltInType01()
## [1] "hierarchical01" "tight"
requiredArgs
The different algorithm types correspond to requiring different input types (k versus alpha). This is usually sorted out by clusterMany, which will only dispatch the appropriate one. Clustering functions can also have additional required arguments. See below for more discussion about how these arguments can be passed along to clusterMany or RSEC.
To see all of the required arguments of a function,
requiredArgs(c("hierarchical01","hierarchicalK"))
## $hierarchical01
## [1] "alpha"
##
## $hierarchicalK
## [1] "k"
Internal clustering procedures
clusterMany iteratively calls a function clusterSingle over the collection of parameters. clusterSingle is the clustering workhorse, and may be used by the user who wants more fine-grained control, see documentation of clusterSingle.
Within each call of clusterSingle, there are three possible steps, depending on the value of the arguments subsample and sequential:
- Subsampling (
subsampleClustering) – if subsample=TRUE
- Main Clustering (
mainClustering)
- Sequential (
seqCluster) – if sequntial=TRUE
If both sequential and subsample are FALSE, then step 1 and step 3 are skipped and clusterSingle just calls the mainClustering (step 2), resulting in a basic clustering routine applied to the input data. If subsample=TRUE, then step 1 (subsampleClustering) is called which subsamples the input data and clusters each subsample to calculate a co-occurance matrix. That co-occurance matrix is used as the input for mainClustering (step 2). If sequential=TRUE this process (step 1 then step 2 if subsample=TRUE or just step 2 if subsample=FALSE) is iterated over and over again to iteratively select the best clusters (see ?seqCluster for a detailed description). Each of these steps has a function that goes with it, noted above, but they should not generally be called directly by the user. However, the documentation of these functions can be useful.
In particular, arguments to these three functions that are not set by clusterMany can be passed via named lists to the arguments: subsampleArgs, mainClusterArgs, and seqArgs. Some of the arguments to these functions can be varied in clusterMany, but more esoteric ones should be sent as part of the named list of parameters given to clusterMany; those named lists will be fixed for all parameter combinations tried in clusterMany.
Main Clustering (Step 2): mainClustering
The main clustering (step 2) described above is done by the function mainClustering. In addition to the basic clustering algorithms on the input data, we also implement many other common cluster processing steps that are relevant to the result of the clustering. We have already seen such an example with dimensionality reduction, where the input \(D\) is determined based on different input data. Many of the arguments to mainClustering are arguments to clusterMany as well so that mainClusterArgs is usually not needed. The main exception would be to send more esoteric arguments to the underlying clustering function called in the main clustering step. The syntax for this would be to give a nested list to the argument mainClusterArgs
clusterMany(x,clusterFunction="hierarchicalK", ... , mainClusterArgs=list(clusterArgs=list(method="single") ))
Here we change the argument method in the clustering function hclust called by the hierarchicalK function to single.
Subsampling (step 1) subsampleClustering
A more significant process that can be coupled with any clustering algorithm is to continually by subsample the data and cluster the subsampled data. This creates a \(n x n\) matrix \(S\) that is a matrix of co-clustering percentages – how many times two samples co-clustered together over the subsamples (there are slight variations as how this can be calculated, see help pages of subsampleClustering ). This does not itself give a clustering, but the resulting \(S\) matrix can then form the basis for clustering the samples. Specifically, the matrix \(D=1-S\) is then given as input to the main clustering step described above. The subsampling option is computationally expensive, and when coupled with comparing many parameters, does result in a lengthy evaluation of clusterMany. However, we recommend it if the number of samples is not too large as one of the most useful methods for getting stable clustering results.
Note that the juxtaposition of step 1 then step 2 (the subsampling and then feeding the results to the main clustering function) implies there actually two different possible clustering algorithms (and sets of corresponding parameters) – one for the clustering on the subsampled data, and one for the clustering of the resulting \(D\) based on the percentage of coClustering of samples. This brings up a restriction on the clustering function in the main clustering step – it needs to be able to handle input that is a dissimilarity (inputType is either diss or either).
Furthermore, the user might want to set clustering function and corresponding parameters separately for step 1 and step 2. The way that clusterMany handles this is that the main arguments of clusterMany focus on varying the parameters related to step 2 (the main clustering step, i.e. the clustering of \(D\) after subsampling). For this reason, the argument clusterFunction in clusterMany varies the clustering function used by the main clustering (step 2), not the subsampling step. The clustering function of the subsampling (step 1) can be specified by the user via subsampleArgs, but in this case it is set for all calls of clusterMany and does not vary. Alternatively, if the user doesn’t specify the clusterFunction in subsampleArgs then the default is to use clusterFunction of the main clustering step along with any required arguments given by the user for that function (there are some cases where using the clusterFunction of the main step is not possible for the subsampling step, in which case the default is to use “pam”).
More generally, since few of the arguments to subsampleClustering are allowed to be varied by the direct arguments to clusterMany, it is also more common to want to change these arguments via the argument subsampleArgs. Examples might be resamp.num (the number of subsamples to draw) or samp.p (the proportion of samples to draw in each subsample) – see ?subsampleClustering for a full documentation of the possible arguments. In addition, there are arguments to be passed to the underlying clustering function; like for mainClustering, these arguments would be a nested list to the argument subsampleArgs.
An example of a syntax that sets the arguments for subsampleClustering would be:
clusterMany(x,..., subsampleArgs=list(resamp.num=100,samp.p=0.5,clusterFunction="hiearchicalK", clusterArgs=list(method="single") ))
Sequential Detection of Clusters (Step 3): seqCluster
Another complicated addition that can be added to the main clustering step is the implementation of sequential clustering. This refers to clustering of the data, then removing the “best” cluster, and then re-clustering the remaining samples, and then continuing this iteration until all samples are clustered (or the algorithm in some other way calls a stop). Such sequential clustering can often be convenient when there is very dominant cluster, for example, that is far away from the other mass of data. Removing samples in these clusters and resampling can sometimes be more productive and result in a clustering more robust to the choice of samples. A particular implementation of such a sequential method, based upon (Tseng and Wong 2005), is implemented in the clusterExperiment package when the option sequential=TRUE is chosen (see ?seqCluster for documentation of how the iteration is done). Sequential clustering can also be quite computationally expensive, particularly when paired with subsampling to determine \(D\) at each step of the iteration.
Because of the iterative nature of the sequential step, there are many possible parameters (see ?seqCluster). Like subsample clustering, clusterMany does not allow variation of very many of these parameters, but they can be set via passing arguments in a named list to seqArgs. An example of a syntax that sets the arguments for seqCluster would be:
clusterMany(x,..., seqArgs=list( remain.n=10))
This code changes the remain.n option of the sequential step, which governs when the sequential step stops because there are not enough samples remaining.
Arguments of clusterMany
Now that we’ve explained the underlying architecture of the clustering provided in the package, and how to set the arguments that can’t be varied, we discuss the parameters that can be varied in clusterMany. (There are a few additional arguments available for clusterMany that govern how clusterMany works, but right now we focus on only the ones that can be given multiple options).
Recall that arguments in clusterMany that take on multiple values mean that the combinations of all the multiple valued arguments will be given as input for a clustering routine. These arguments are:
sequential This parameter consists of logical values, TRUE and/or FALSE, indicating whether the sequential strategy should be implemented or not.subsample This parameter consists of logical values, TRUE and/or FALSE, indicating whether the subsampling strategy for determining \(D\) should be implemented or not.clusterFunction The clustering functions to be tried in the main clustering step. Recall if subsample=TRUE is part of the combination, then clusterFunction the method that will be used on the matrix \(D\) created from subsampling the data. Otherwise, clusterFunction is the clustering method that will be used directly on the data.ks The argument ‘ks’ is interpreted differently for different choices of the other parameters and can differ from between parameter combinations!. If sequential=TRUE is part of the parameter combination, ks defines the argument k0 of sequential clustering (see ?seqCluster), which is approximately like the initial starting point for the number of clusters in the sequential process. Otherwise, ks is passed to set k of both the main clustering step (and by default that of the subsampled data), and is only relevant if clusterFunction is of type “K”. When/if findBestK=TRUE is part of the combination, ks also defines the range of values to search for the best k (see the details in the documentation of clusterMany for more).reduceMethod These are character strings indicating what choices of dimensionality reduction should be tried. These can indicate any combination of either filtering statistics or dimensionality reductions. The character strings can either refer to built-in methods, meaning clusterMany will do the necessary calculations and save the results as an initial step, OR the vector can refer to filtering statistics/dimensionality reductions that have already been calculated and saved in the object (see (above)[#dimReduce] for more information). The vector cannot be a combination of these two.
If either a dimensionality reduction or a filtering statistic are chosen, the following parameters can also be varied to indicate the number of such features to be used (with a vector of values meaning all will be tried):
distFunction These are character values giving functions that provide a distance matrix between the samples, when applied to the data. These functions should be accessible in the global environment (clusterMany applies get to the global environment to access these functions). To make them compatible with the standard R function dist, these functions should assume the samples are in the rows, i.e. they should work when applied to t(assay(ce)). We give an example in the next subsection below.minSizes these are integer values determining the minimum size required for a cluster (passed to the mainClustering part of clustering).alphas These are the \(\alpha\) parameters for “01” clustering techniques; these values are only relevant if one of the clusterFunction values is a “01” clustering algorithm. The values given to alphas should be between 0 and 1, with smaller values indicating greater similarity required between the clusters.betas These are the \(\beta\) parameters for sequential clustering; these values are only relevant if sequential=TRUE and determine the level of stability required between changes in the parameters to determine that a cluster is stable.findBestK This option is for “K” clustering techniques, and indicates that \(K\) should be chosen automatically as the \(K\) that gives the largest silhouette distance between clusters.removeSil A logical value as to whether samples with small silhouette distance to their assigned cluster are “removed”, in the sense that they are not given their original cluster assignment but instead assigned -1. This option is for “K” clustering techniques as a method of removing poorly clustered samples.
silCutoff If removeSil is TRUE, then silCutoff determines the cutoff on silhouette distance for unassigning the sample.
clusterMany tries to have generally simple interface, and for this reason makes choices about what is meant by certain combinations of parameters. For example, in combinations where findBestK=TRUE, ks=2:10 is taken to mean that the clustering should find the best \(k\) out of the range of 2-10. However, in other parameter combinations where findBestK=FALSE the same ks might indicate the specific number of clusters, \(K\), that should be found. To see the parameter choices that will be run, the user can set run=FALSE and the output will be a matrix of the parameter values indicated by the choices of the user. For parameter combinations that are not what is desired, the user should consider making direct calls to clusterSingle where all of these options combinations (and many more) can be explicitly called.
Other parameters for the clustering are kept fixed. As described above, there are many more possible parameters in play than are considered in clusterMany. These parameters can be set via the arguments mainClusterArgs, subsampleArgs and seqArgs. These arguments correspond to the different processes described above (the main clustering step, the creation of \(D\) to be clustered via subsampling, and the sequential clustering process, respectively). These arguments take a list of arguments that are sent directly to clusterSingle. However, these arguments may be overridden by the interpretation of clusterMany of how different combinations interact; again for complete control direct calls to clusterSingle are necessary.
| ks |
sequential=TRUE |
seqCluster |
k0 |
| - |
sequential=FALSE, findBestK=FALSE, clusterFunction of type ‘K’ |
mainClustering |
k |
| - |
sequential=FALSE, findBestK=FALSE, subsample=TRUE |
subsampleClustering |
k |
| - |
sequential=FALSE, findBestK=TRUE, clusterFunction of type ‘K’ |
mainClustering |
kRange |
| reduceMethod |
none |
transform |
reduceMethod |
| nFilterDims |
reduceMethod in ‘mad’,‘cv’,‘var’ |
transform |
nFilterDims |
| nReducedDims |
reduceMethod=‘PCA’ |
transform |
nReducedDims |
| clusterFunction |
none |
mainClustering |
clusterFunction |
| minSizes |
none |
mainClustering |
minSize |
| distFunction |
subsample=FALSE |
mainClustering |
distFunction |
| alphas |
clusterFunction of type ‘01’ |
mainClustering |
alpha |
| findBestK |
clusterFunction of type ‘K’ |
mainClustering |
findBestK |
| removeSil |
clusterFunction of type ‘K’ |
mainClustering |
removeSil |
| silCutoff |
clusterFunction of type ‘K’ |
mainClustering |
silCutoff |
| betas |
sequential=TRUE |
seqCluster |
beta |
Example changing the distance function
Providing different distance functions is slightly more involved than the other parameters, so we give an example here.
First we define distances that we would like to compare. We are going to define two distances that take values between 0-1 based on different choices of correlation.
corDist<-function(x){(1-cor(t(x),method="pearson"))/2}
spearDist<-function(x){(1-cor(t(x),method="spearman"))/2}
These distances are defined so as to give distance of 0 between samples with correlation 1, and distance of 1 for correlation -1.
We will also compare using different algorithms for clustering. Currently, clusterMany requires that the distances work with all of the clusterFunction choices given. Since some of the clusterFunction algorithms require a distance matrix between 0-1, this means we can only compare all of the algorithms when the distance is a 0-1 distance. (Future versions may try to create a work around so that the algorithm just skips algorithms that don’t match the distance). Since the distances we defined are between 0-1, however, we can use any algorithm that takes dissimilarities as input.
Note on 0-1 clustering when subsample=FALSE We would note that the default values of \(\alpha\) in clusterMany and RSEC for the 0-1 clustering were set with the distance \(D\) the result of subsampling or other concensus summary in mind. In generally, subsampling creates a \(D\) matrix with high similarity for many samples who share a cluster (the proportion of times samples are seen together for well clustered samples can easily be in the .8-.95 range, or even exactly 1). For this reason the default \(\alpha\) is 0.1 which requires distances between samples in the 0.1 range or less (i.e. a similarity in the range of 0.9 or more).
To illustrate this point, we show an example of the \(D\) matrix from subsampling. To do this we make use of the clusterSingle which is the workhorse mentioned above that runs a single clustering command directly; it gives the output \(D\) from the sampling in the “coClustering” slot of ce when we set replaceCoCluster=TRUE (and therefore we save it as a separate object, so that it doesn’t write over the existing “coClustering” slot in ce). Note that the result is \(1-p_{ij}\) where \(p_{ij}\) is the proportion of times sample \(i\) and \(j\) clustered together.
ceSub<-clusterSingle(ce,reduceMethod="mad",nDims=1000,subsample=TRUE,subsampleArgs=list(clusterFunction="pam",clusterArgs=list(k=8)),clusterLabel="subsamplingCluster",mainClusterArgs=list(clusterFunction="hierarchical01",clusterArgs=list(alpha=0.1),minSize=5), saveSubsamplingMatrix=TRUE)
plotCoClustering(ceSub,colorScale=rev(seqPal5))
We see even here, the default of \(\alpha=0.1\) was perhaps too conservative since only two clusters came out (at leastwith size greater than 5).
However, the distances based on correlation calculated directly on the data, such as we created above, are also often used for clustering expression data directly (i.e. without the subsampling step). But they are unlikely to have dissimilarities as low as seen in subsampling, even for well clustered samples. Here’s a visualization of the correlation distance matrix we defined above (using Spearman’s correlation) on the top 1000 most variable features:
dSp<-spearDist(t(transformData(ce,reduceMethod="mad",nFilterDims=1000)))
plotHeatmap(dSp,isSymmetric=TRUE,colorScale=rev(seqPal5))
We can see that the choice of \(\alpha\) must be much higher (and we are likely to be more sensitive to it).
Notice to calculate the distance in the above plot, we made use of the transform function applied to our ce object to get the results of dimensionality reduction. The transform function gave us a data matrix back that has been transformed, and also reduced in dimensions, like would be done in our clustering routines. transform has similar parameters as seen in clusterMany,makeDendrogram or clusterSingle and is useful when you want to manually apply something to transformed and/or dimensionality reduced data; and you can be sure you are getting the same matrix of data back that the clustering algorithms are using.
Comparing distance functions with clusterMany Now that we have defined the distances we want to compare in our global environment, we can give these to the argument “distFunction” in clusterMany. They should be given as character strings giving the names of the functions. For computational ease for this vignette, we will just choose the dimensionality reduction to be the top 1000 features based on MAD and set K=8 or \(\alpha=0.45\).
Since we haven’t yet calculated “mad” on this object, it hasn’t been calculated yet. clusterMany does not let you mix and match between uncalculated and stored filters (or dimensionality reductions), so our first step is to store the mad results. We will save these results as a separate object so as to not disrupt the earlier workflow.
ceDist<-makeFilterStats(ce,filterStats="mad")
ceDist
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final mad
## -----------
## Primary cluster type: mergeClusters
## Primary cluster label: mergeClusters
## Table of clusters (of primary clustering):
## -1 m01 m02 m03 m04
## 6 15 14 13 17
## Total number of clusterings: 41
## Dendrogram run on 'makeConsensus,final' (cluster index: 2)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? Yes
ceDist<-clusterMany(ceDist, k=7:9, alpha=c(0.35,0.4,0.45),
clusterFunction=c("tight","hierarchical01","pam","hierarchicalK"),
findBestK=FALSE,removeSil=c(FALSE),dist=c("corDist","spearDist"),
reduceMethod=c("mad"),nFilterDims=1000,run=TRUE)
clusterLabels(ceDist)<-gsub("clusterFunction","alg",clusterLabels(ceDist))
clusterLabels(ceDist)<-gsub("Dist","",clusterLabels(ceDist))
clusterLabels(ceDist)<-gsub("distFunction","dist",clusterLabels(ceDist))
clusterLabels(ceDist)<-gsub("hierarchical","hier",clusterLabels(ceDist))
par(mar=c(1.1,15.1,1.1,1.1))
plotClusters(ceDist,axisLine=-2,colData=c("Biological_Condition"))
Notice that using the “tight” methods did not give relevant results (no samples were clustered)
Example using a user-defined clustering algorithm
Here, we show how to use a user-defined clustering algorithm in clusterSingle. Our clustering algorithm will be a simple nearest-neighbor clustering.
To do so, we need to create a ClusterFunction object that defines our algorithm. ClusterFunction objects recognize clustering algorithms of two different types, based on the required input from the user: 01 or K (see (ClusterFunction)[#ClusterFunction] section above for more). Type K refers to a clustering algorithm where the user must specify the number of clusters as input parameter, and this is the type of algorithm we will implement (though as we’ll see, in fact our clustering algorithm doesn’t have the user specify the number of clusters…).
First, we need to define a wrapper function that performs the clustering. Here, we define a simple shared nearest-neighbor clustering using functions from the scran and the igraph packages.
library(scran)
library(igraph)
SNN_wrap <- function(x, k, steps = 4, ...) {
snn <- buildSNNGraph(x, k = k, d = NA, transposed = FALSE) ##scran package
res <- cluster_walktrap(snn, steps = steps) #igraph package
return(res$membership)
}
Here the argument k defines the number of nearest-neighbors to use in constructing the nearest neighbor graph.
To create a type K algorithm, the wrapper must have two required arguments:
- an argument for the input data. This can be
x if the input is a matrix of \(N\) samples on the columns and features on the rows, or diss if the input is expected to be a \(NxN\) dissimilarity matrix. Both x and diss can be given as parameters if the algorithm handles either one)
- a parameter
k specifying the number of clusters (or any other integer-valued parameter that the clustering relies on)
Our k value for SNN_wrap will not in fact specify the number of clusters, but that is not actually required anywhere. But setting it up as type K mainly distinguishes it from the 01 type (which expects a dissimilarity matrix taking values between 0 and 1 in its dissimilarity entries, as input). Also setting it up as type K allows us to use the findBestK option, where a range of k values is tried and those with the best results (in silhouette width) is reported.
Our wrapper function should return a integer vector corresponding to the cluster assignments of each sample (see ?ClusterFunction for information about other types of output available).
clusterExperiment provides the function internalFunctionCheck that validates user-defined cluster functions. Among other things, it checks that the input and output are compatible with the clusterExperiment workflow (see ?internalFunctionCheck for details). The call to internalFunctionCheck contains, in addition to the function definition, arguments specifying information about the type of input, the type of algorithm, and type of output expected by the function. This information is passed to clusterMany and clusterSingle so that they know what to pass and what to expect from the user-defined method.
internalFunctionCheck(SNN_wrap, inputType = "X", algorithmType = "K",
outputType="vector")
## [1] TRUE
If it passes all checks (returns TRUE), we can then create an object of the S4 class ClusterFunction to be used within the package using this same set of arguments. If it fails, it will return a character string giving the error. Among the checks is running the function on a small randomly generated set of data, so the errors may not be about the format of the function, but also whether the series of code runs.
Since we passed the checks, we are ready to define our ClusterFunction object.
SNN <- ClusterFunction(SNN_wrap, inputType = "X", algorithmType = "K",
outputType="vector")
Now that we have our object SNN, we can treat our custom method as a base clustering routine to be used in clusterMany, similarly to how we used kmeans and pam earlier. However, unlike before, you should pass the actual object SNN, and not a quoted version (i.e. not "SNN").
In this example, we use clusterSingle to implement a subsample clustering based on SNN. clusterSingle is useful if you just want to create a single clustering.
We give SNN to the subsampleArgs that will be passed to the subsampling. (Note that to create a consensus clustering from the different subsamplings we use a different function, "hierarchical01", that is passed to mainClusterArgs),
ceCustom <- clusterSingle(
ce, reduceMethod="PCA", nDims=50,
subsample = TRUE, sequential = FALSE,
mainClusterArgs = list(clusterFunction = "hierarchical01",
clusterArgs = list(alpha = 0.3),
minSize = 1),
subsampleArgs = list(resamp.num=100,
samp.p = 0.7,
clusterFunction = SNN,
clusterArgs = list(k = 10),
ncores = 1)
)
ceCustom
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final
## -----------
## Primary cluster type: clusterSingle
## Primary cluster label: clusterSingle
## Table of clusters (of primary clustering):
## 1 2 3 4
## 33 30 1 1
## Total number of clusterings: 42
## Dendrogram run on 'makeConsensus,final' (cluster index: 2)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? Yes
Similarly, we can use clusterMany to compute clusters using many different methods, including built-in and custom functions. To mix and match built-in functions, you need to get the actual ClusterFunction objects that match their names, using the getBuiltInFunction function.
clFuns<-getBuiltInFunction(c("pam","kmeans"))
Then we will add our function to the list of functions. Note that it is important we give a name to every element of the list, including our new function!
clFuns<-c(clFuns, "SNN"=SNN)
Now we can give this list of functions to clusterMany
ceCustom <- clusterMany(ce, dimReduce="PCA",nPCADims=50,
clusterFunction=clFuns,
ks=4:15, findBestK=FALSE)
Note that if I call getBuiltInFunction for only one cluster function, it returns the actual ClusterFunction object, not a list of length 1. To combine it with other functions you need to make it into a list.
Dealing with large numbers of clusterings
A good first check before running clusterMany is to determine how many clusterings you are asking for. clusterMany has some limited internal checks to not do unnecessary duplicates (e.g. removeSil only works with some clusterFunctions so clusterMany would detect that), but generally takes all combinations. This can take a while for more complicated clustering techniques, so it is a good idea to check what you are getting into. You can do this by running clusterMany with run=FALSE.
In the following we consider expanding our original clustering choices to consider individual choices of \(K\) (rather than just findBestK=TRUE).
checkParam<-clusterMany(se, clusterFunction="pam", ks=2:10,
removeSil=c(TRUE,FALSE), isCount=TRUE,
reduceMethod=c("PCA","var"),
nFilterDims=c(100,500,1000),nReducedDims=c(5,15,50),run=FALSE)
dim(checkParam$paramMatrix) #number of rows is the number of clusterings
## [1] 108 14
Each row of the matrix checkParam$paramMatrix is a requested clustering (the columns indicate the value of a possible parameter). Our selections indicate 108 different clusterings (!).
We can set ncores argument to have these clusterings done in parallel. If ncores>1, the parallelization is done via mclapply and should not be done in the Rgui interface (see help pages for mclapply).
Create a unified cluster from many clusters with makeConsensus
After creating many clusterings, makeConsensus finds a single cluster based on what samples were in the same clusters throughout the many clusters found by clusterMany. While subsampling the data helps be robust to outlying samples, combining across many clustering parameters can help be robust to choice in parameters, particularly when the parameters give roughly similar numbers of clusters.
As mentioned in the Quick Start section, the default option for makeConsensus is to only define a cluster when all of the samples are in the same clusters across all clusterings. However, this is generally too conservative and just results in most samples not being assigned to a cluster.
Instead makeConsensus has a parameter proportion that governs in what proportion of clusterings the samples should be together. Internally, makeConsensus makes a coClustering matrix \(D\). Like the \(D\) created by subsampling in clusterMany, the coClustering matrix takes on values 0-1 for the proportion of times the samples are together in the clustering. This \(D\) matrix is saved in the ce object and can be visualized with plotCoClustering (which is just a call to plotHeatmap). Recall the one we last made in the QuickStart, with our last call to makeConsensus (proportion=0.7 and minSize=3).
plotCoClustering(ce)
makeConsensus performs the clustering by running a “01” clustering algorithm on the \(D\) matrix of percentage co-clustering (the default being “hierarchical01”). The alpha argument to the 01 clustering is 1-proportion. Also passed to the clustering algorithm is the parameter minSize which sets the minimum size of a cluster.
Treatment of Unclustered assignments -1 values are treated separately in the calculation. In particular, they are not considered in the calculation of percentage co-clustering – the percent co-clustering is taken only with respect to those clusterings where both samples were assigned. However, a post-processing is done to the clusters found from running the clustering on the \(D\) matrix. For each sample, the percentage of times that they were marked -1 in the clusterings is calculated. If this percentage is greater than the argument propUnassigned then the sample is marked as -1 in the clustering returned by makeConsensus.
Good scenarios for running makeConsensus Varying certain parameters result in clusterings better for makeConsensus than other sets of parameters. In particular, if there are huge discrepancies in the set of clusterings given to makeConsensus, the results will be a shattering of the samples into many small clusters. Similarly, if the number of clusters \(K\) is very different, the end result will likely be like that of the large \(K\), and how much value that is (rather than just picking the clustering with the largest \(K\)), is debatable. However, for “01” clustering algorithms or clusterings using the sequential algorithm, varying the underlying parameters \(\alpha\) or \(k_0\) often results in roughly similar clusterings across the parameters so that creating a consensus across them is highly informative.
Consensus from subsets of clusterings
A call to clusterMany or to RSEC can generate many clusterings that result from changing the underlying parameters of a given method (e.g., the number of centers in k-means), the dimensionality reduction, the distance function, or the base algorithm used for the clustering (e.g., PAM vs. k-means).
To highlight interesting structure in the data, it may be useful to understand whether a set of samples tends to cluster together across paramter choices of the same method or across very different methods.
clusterExperiment makes it easy to extract a subset of clusterings and to compute a consensus clustering for any given subset, to help addressing this type of questions, as we have already seen in the section on makeConsensus.
As an example, assume that we want to explore the role of PCA in the clustering results. We can separately calculate a consensus of those clusterings that used 15 or 50 principal components of the data.
First, we use the getClusterManyParams function to extract the information on the clusterings performed.
params <- getClusterManyParams(ce)
head(params)
## clusteringIndex
## reduceMethod=PCA,nReducedDims=5,nFilterDims=NA,k=5 5
## reduceMethod=var,nReducedDims=NA,nFilterDims=100,k=5 6
## reduceMethod=PCA,nReducedDims=15,nFilterDims=NA,k=5 7
## reduceMethod=PCA,nReducedDims=50,nFilterDims=NA,k=5 8
## reduceMethod=var,nReducedDims=NA,nFilterDims=500,k=5 9
## reduceMethod=var,nReducedDims=NA,nFilterDims=1000,k=5 10
## reduceMethod
## reduceMethod=PCA,nReducedDims=5,nFilterDims=NA,k=5 PCA
## reduceMethod=var,nReducedDims=NA,nFilterDims=100,k=5 var
## reduceMethod=PCA,nReducedDims=15,nFilterDims=NA,k=5 PCA
## reduceMethod=PCA,nReducedDims=50,nFilterDims=NA,k=5 PCA
## reduceMethod=var,nReducedDims=NA,nFilterDims=500,k=5 var
## reduceMethod=var,nReducedDims=NA,nFilterDims=1000,k=5 var
## nReducedDims
## reduceMethod=PCA,nReducedDims=5,nFilterDims=NA,k=5 5
## reduceMethod=var,nReducedDims=NA,nFilterDims=100,k=5 NA
## reduceMethod=PCA,nReducedDims=15,nFilterDims=NA,k=5 15
## reduceMethod=PCA,nReducedDims=50,nFilterDims=NA,k=5 50
## reduceMethod=var,nReducedDims=NA,nFilterDims=500,k=5 NA
## reduceMethod=var,nReducedDims=NA,nFilterDims=1000,k=5 NA
## nFilterDims k
## reduceMethod=PCA,nReducedDims=5,nFilterDims=NA,k=5 NA 5
## reduceMethod=var,nReducedDims=NA,nFilterDims=100,k=5 100 5
## reduceMethod=PCA,nReducedDims=15,nFilterDims=NA,k=5 NA 5
## reduceMethod=PCA,nReducedDims=50,nFilterDims=NA,k=5 NA 5
## reduceMethod=var,nReducedDims=NA,nFilterDims=500,k=5 500 5
## reduceMethod=var,nReducedDims=NA,nFilterDims=1000,k=5 1000 5
We can select only the clusterings in which we are interested in and pass them to makeConsensus using the whichClusters argument.
clusterIndices15 <- params$clusteringIndex[which(params$nReducedDims == 15)]
clusterIndices50 <- params$clusteringIndex[which(params$nReducedDims == 50)]
#note, the indices will change as we add clusterings!
clusterNames15 <- clusterLabels(ce)[clusterIndices15]
clusterNames50 <- clusterLabels(ce)[clusterIndices50]
shortNames15<-gsub("reduceMethod=PCA,nReducedDims=15,nFilterDims=NA,","",clusterNames15)
shortNames50<-gsub("reduceMethod=PCA,nReducedDims=50,nFilterDims=NA,","",clusterNames50)
ce <- makeConsensus(ce, whichClusters = clusterNames15, proportion = 0.7,
clusterLabel = "consensusPCA15")
ce <- makeConsensus(ce, whichClusters = clusterNames50, proportion = 0.7,
clusterLabel = "consensusPCA50")
Analogously, we’ve seen that many visualization functions have a whichClusters argument that can be used to visually inspect the similarities and differences between subsets of clusterings.
Here we show using this features with plotClustersWorkflow for the two different consensus clusterings we made.
par(mar=plotCMar,mfrow=c(1,2))
plotClustersWorkflow(ce, whichClusters ="consensusPCA15",clusterLabel="Consensus",whichClusterMany=match(clusterNames15,clusterLabels(ceSub)),clusterManyLabels=c(shortNames15),axisLine=-1,nBlankLines=1,main="15 PCs")
plotClustersWorkflow(ce, whichClusters = c("consensusPCA50"),clusterLabel="Consensus",clusterManyLabels=shortNames50, whichClusterMany=match(clusterNames50,clusterLabels(ceSub)),nBlankLines=1,main="50 PCs")
We can also choose a subset and vary the parameters
wh<-getClusterManyParams(ce)$clusteringIndex[getClusterManyParams(ce)$reduceMethod=="var"]
ce<-makeConsensus(ce,whichCluster=wh,proportion=0.7,minSize=3,
clusterLabel="makeConsensus,nVAR")
plotCoClustering(ce)
We can compare to all of our other versions of makeConsensus. While they do not all have clusterTypes equal to “makeConsensus” (only the most recent call has clusterType exactly equal to “makeConsensus”), they all have “makeConsensus” as part of their clusterType, even though they have different clusterLabels (and now we’ll see that it was useful to give them different labels!)
wh<-grep("makeConsensus",clusterTypes(ce))
par(mar=plotCMar)
plotClusters(ce,whichClusters=rev(wh),axisLine=-1)
Creating a Hierarchy of Clusters with makeDendrogram
As mentioned above, we find that merging clusters together based on the extent of differential expression between the features to be a useful method for combining many small clusters.
We provide a method for doing this that consists of two steps. Making a hierarchy between the clusterings and then estimating the amount of differential expression at each branch of the hierarchy.
makeDendrogram creates a hierarchical clustering of the clusters as determined by the primaryCluster of the ClusterExperiment object. In addition to being used for merging clusters, the dendrograms created by makeDendrogram are also useful for ordering the clusters in plotHeatmap as has been shown above.
makeDendrogam performs hierarchical clustering of the cluster medoids (after transformation of the data) and provides a dendrogram that will order the samples according to this clustering of the clusters. The hierarchical ordering of the dendrograms is saved internally in the ClusterExperiment object.
Like clustering, the dendrogram can depend on what features are included from the data. The same options for clustering are available for the hierarchical clustering of the clusters, namely choices of dimensionality reduction via reduceMethod and the number of dimensions via nDims.
ce<-makeDendrogram(ce,reduceMethod="var",nDims=500)
plotDendrogram(ce)
Notice that the plot of the dendrogram shows the hierarchy of the clusters (and color codes them according to the colors stored in colorLegend slot).
Recall that the most recent clustering made is from our call to makeConsensus, where we experimented with using on some of the clusterings from clusterMany, so that is our current primaryCluster:
show(ce)
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final var_makeConsensus.nVAR
## -----------
## Primary cluster type: makeConsensus
## Primary cluster label: makeConsensus,nVAR
## Table of clusters (of primary clustering):
## -1 c01 c02 c03 c04 c05 c06 c07
## 10 15 13 9 7 5 3 3
## Total number of clusterings: 44
## Dendrogram run on 'makeConsensus,nVAR' (cluster index: 1)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? No
This is the clustering from combining only the clusterings from clusterMany that use the top most variable genes. Because it is the primaryCluster, it was the clustering that was used by default to make the dendrogram.
We might prefer to get back to the dendrogram based on our makeConsensus in quick start (the “makeConsensus, final” clustering). We’ve lost that dendrogram when we called makeDendrogram again. However, we can rerun makeDendrogram and choose a different clustering from which to make the dendrogram.
ce<-makeDendrogram(ce,reduceMethod="var",nDims=500,
whichCluster="makeConsensus,final")
We will visualize the dendrogram with plotDendrogram. The default setting plots the dendrogram where there are color blocks equal to the size of the clusters (i.e number of samples in each cluster).
plotDendrogram(ce,leafType="sample",plotType="colorblock")
We can actually use plotDendrogram to compare clusterings too, like plotClusters using the whichClusters argument to identfy which clusters to show. For example, lets compare our different makeConsensus results
par(mar=plotDMar)
whCM<-grep("makeConsensus",clusterTypes(ce))
plotDendrogram(ce,whichClusters=whCM,leafType="sample",plotType="colorblock")
Unlike plotClusters, however, there is no aligning of samples to make samples with the same cluster group together.
Making a past run the current one.
Note that because we’ve run additional makeConsensus steps on this data, the clustering we originally designated as “final” is not our primary cluster. Instead our most recent call to makeConsensus is the primary cluster:
primaryClusterLabel(ce)
## [1] "makeConsensus,nVAR"
show(ce)
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final var_makeConsensus.nVAR
## -----------
## Primary cluster type: makeConsensus
## Primary cluster label: makeConsensus,nVAR
## Table of clusters (of primary clustering):
## -1 c01 c02 c03 c04 c05 c06 c07
## 10 15 13 9 7 5 3 3
## Total number of clusterings: 44
## Dendrogram run on 'makeConsensus,final' (cluster index: 5)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? No
We know the results are still saved. If we search for the label we gave it, we can find it (given by clusterLabel). And if we look at its value in clusterTypes it doesn’t even have its clusterTypes as makeConsensus, but instead has a “.x” value appended to it (see )
whFinal<-which(clusterLabels(ce)=="makeConsensus,final")
head(clusterMatrix(ce,whichCluster=whFinal))
## makeConsensus,final
## SRR1275356 -1
## SRR1275251 -1
## SRR1275287 6
## SRR1275364 4
## SRR1275269 6
## SRR1275263 5
clusterTypes(ce)[whFinal]
## [1] "makeConsensus.3"
But rather than continually refinding the cluster, we can choose to reset this past call to makeConsensus to be the current ‘makeConsensus’ output (which will also set this clustering to be the primaryCluster).
ce<-setToCurrent(ce,whichCluster="makeConsensus,final")
show(ce)
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final var_makeConsensus.nVAR
## -----------
## Primary cluster type: makeConsensus
## Primary cluster label: makeConsensus,final
## Table of clusters (of primary clustering):
## -1 c01 c02 c03 c04 c05 c06 c07
## 6 15 14 9 8 5 4 4
## Total number of clusterings: 44
## Dendrogram run on 'makeConsensus,final' (cluster index: 5)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? No
We don’t need to recall makeDendrogram, since in our call to makeDendrogram we explicitly set the argument whichCluster to make the dendrogram from this clustering.
More about how the dendrogram is saved
The resulting dendrograms (one for just the cluster hierarchy and one that expands the cluster hierarchy to include the samples) are saved in the object. They are each saved as a phylo4d class from the package phylobase (which uses the basic format of the S3 class phylo in the ape package, but is a S4 class with some useful helpers).
They can be accessed with the functions clusterDendrogram and sampleDendrogram.
clusterDendrogram(ce)
## label node ancestor edge.length node.type NodeId ClusterIdDendro
## 1 T1 1 10 6818.1055 tip NodeId7 ClusterId1
## 2 T2 2 9 4792.5997 tip NodeId8 ClusterId2
## 3 T3 3 11 4699.3992 tip NodeId9 ClusterId3
## 4 T4 4 13 3667.0646 tip NodeId10 ClusterId4
## 5 T5 5 12 4172.1952 tip NodeId11 ClusterId5
## 6 T6 6 11 4699.3992 tip NodeId12 ClusterId6
## 7 T7 7 13 3667.0646 tip NodeId13 ClusterId7
## 8 NodeId1 8 0 NA root NodeId1 <NA>
## 9 NodeId2 9 8 4803.5659 internal NodeId2 <NA>
## 10 NodeId3 10 8 2778.0601 internal NodeId3 <NA>
## 11 NodeId4 11 10 2118.7062 internal NodeId4 <NA>
## 12 NodeId5 12 9 620.4044 internal NodeId5 <NA>
## 13 NodeId6 13 12 505.1306 internal NodeId6 <NA>
## ClusterIdMerge Position
## 1 NA cluster hierarchy tip
## 2 NA cluster hierarchy tip
## 3 NA cluster hierarchy tip
## 4 NA cluster hierarchy tip
## 5 NA cluster hierarchy tip
## 6 NA cluster hierarchy tip
## 7 NA cluster hierarchy tip
## 8 NA cluster hierarchy node
## 9 NA cluster hierarchy node
## 10 NA cluster hierarchy node
## 11 NA cluster hierarchy node
## 12 NA cluster hierarchy node
## 13 NA cluster hierarchy node
head(sampleDendrogram(ce))
## label node ancestor edge.length node.type NodeId Position SampleIndex
## 1 T01 1 73 0 tip <NA> assigned tip 8
## 2 T02 2 80 0 tip <NA> assigned tip 9
## 3 T03 3 81 0 tip <NA> assigned tip 10
## 4 T04 4 82 0 tip <NA> assigned tip 18
## 5 T05 5 83 0 tip <NA> assigned tip 24
## 6 T06 6 84 0 tip <NA> assigned tip 26
## 7 T07 7 85 0 tip <NA> assigned tip 27
## 8 T08 8 86 0 tip <NA> assigned tip 28
## 9 T09 9 87 0 tip <NA> assigned tip 42
## 10 T10 10 88 0 tip <NA> assigned tip 43
## 11 T11 11 89 0 tip <NA> assigned tip 45
## 12 T12 12 90 0 tip <NA> assigned tip 46
## 13 T13 13 91 0 tip <NA> assigned tip 53
## 14 T14 14 92 0 tip <NA> assigned tip 58
## 15 T15 15 92 0 tip <NA> assigned tip 59
## 16 T16 16 74 0 tip <NA> assigned tip 11
## 17 T17 17 93 0 tip <NA> assigned tip 12
## 18 T18 18 94 0 tip <NA> assigned tip 14
## 19 T19 19 95 0 tip <NA> assigned tip 21
## 20 T20 20 96 0 tip <NA> assigned tip 22
Just like the clusters, the nodes have permanent non-changing names (stored in the NodeId column). The dendrograms also store information on how to match the dendrogram to the clusters (and if applicable the merged clusters). To see more about the information saved in these dendrograms, see ?clusterDendrogram.
Generally, these dendrograms will not need to be directly manipulated by the user. But if desired, the user can explore these objects using the functions in phylobase.
library(phylobase)
nodeLabels(clusterDendrogram(ce))
## 8 9 10 11 12 13
## "NodeId1" "NodeId2" "NodeId3" "NodeId4" "NodeId5" "NodeId6"
descendants(clusterDendrogram(ce),node="NodeId3")
## T1 T3 T6
## 1 3 6
The main reason to really ever work with these dendrograms directly is to link it back with the (merging results)[#mergeClusters] or (feature extraction results)[#Dendrocontrasts]. In particular, one feature of the cluster dendrogram can be set by the user is the labels for the internal nodes of the cluster hierarchy. Because of this there is a function nodeLabels that can be called directly on the ClusterExperiment object to see and update these values. Unlike our previous code, where we extracted the dendrogram and then used the functions in phylobase to look at it, these functions will update the actual dendrograms inside the object.
We’ll demonstrate this by giving the nodes new names that are the letters A-Z. The main trick in creating new node labels, is that it is required that the new replacement vector of names have names that match the internal node ids (the NodeId column).
newNodeLabels<-LETTERS[1:6]
names(newNodeLabels)<-nodeLabels(ce)
nodeLabels(ce)<-newNodeLabels
Merging clusters with mergeClusters
We then can use this hierarchy of clusters to merge clusters that show little difference in expression. We do this by testing, for each node of the dendrogram, for which features is the mean of the set of clusters to the right split of the node is equal to the mean on the left split. This is done via the getBestFeatures (see section on getBestFeatures), where the type argument is set to “Dendro”.
Starting at the bottom of the tree, those clusters that have the percentage of features with differential expression below a certain value (determined by the argument cutoff) are merged into a larger cluster. This testing of differences and merging continues until the estimated percentage of non-null DE features is above cutoff. This means lower values of cutoff result in less merging of clusters. There are multiple methods of estimation of the percentage of non-null features implemented. The option mergeMethod="adjP" which we showed earlier is the simplest: the proportion found significant by calculating the proportion of DE genes a given False Discovery Rate threshold of 0.05 (using the Benjamini-Hochberg procedure). However, other more sophisticated methods are also implemented (see ?mergeClusters).
Notice that mergeClusters will always run based on the clustering that made the currently existing dendrogram. So it is always good to check that it is what we expect.
ce
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final var_makeConsensus.nVAR
## -----------
## Primary cluster type: makeConsensus
## Primary cluster label: makeConsensus,final
## Table of clusters (of primary clustering):
## -1 c01 c02 c03 c04 c05 c06 c07
## 6 15 14 9 8 5 4 4
## Total number of clusterings: 44
## Dendrogram run on 'makeConsensus,final' (cluster index: 5)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? No
We see in the summary “Dendrogram run on ‘makeConsensus,final’”, showing us that this is the clustering that will be used (and also showing us the value of giving our own labels to the results of makeConsensus if we are going to try different strategies).
We will run mergeClusters with the option mergeMethod="adjP". We will also set plotInfo="adjP" meaning that we would like the mergeClusters command to also produce a plot showing the dendrogram and the estimates from the adjP method for each node. We also set calculateAll=FALSE for illustration purposes, meaning the function will only calculate the estimates for the methods we request, but as we explain below, that is not necessarily the best option if you are going to be trying out different cutoffs.
ce<-mergeClusters(ce,mergeMethod="adjP",plotInfo=c("adjP"),calculateAll=FALSE)
The info about the merge is saved in the ce object.
mergeMethod(ce)
## [1] "adjP"
mergeCutoff(ce)
## [1] 0.05
nodeMergeInfo(ce)
## NodeId Contrast isMerged mergeClusterId Storey PC
## 1 NodeId1 (X2+X5+X4+X7)/4-(X1+X3+X6)/3 FALSE NA NA NA
## 2 NodeId2 X2-(X5+X4+X7)/3 FALSE NA NA NA
## 3 NodeId3 X1-(X3+X6)/2 FALSE NA NA NA
## 4 NodeId4 X3-X6 TRUE 3 NA NA
## 5 NodeId5 X5-(X4+X7)/2 TRUE 4 NA NA
## 6 NodeId6 X4-X7 TRUE NA NA NA
## adjP locfdr MB JC
## 1 0.12137502 NA NA NA
## 2 0.09478003 NA NA NA
## 3 0.05658509 NA NA NA
## 4 0.01938039 NA NA NA
## 5 0.03437544 NA NA NA
## 6 0.02447305 NA NA NA
Notice that nodeMergeInfo gives for each node the proportion estimated to be differentially expressed at each node (as displayed in the plot that we requested), as well as whether that node was merged together in the mergeClusters call (the isMerged column). Because we set calculateAll=FALSE only the methods needed for our command were calculated (adjP). The others have NA values. The column mergeClusterId tells us which nodes in the tree are now equivalent to a cluster; this is different than the isMerged column, since some nodes can be merged but if their parent nodes were also merged, then that node will not be equivalent to a cluster in the “mergeClusters” clustering. (See Dendrogram Contrats above for more information about the nodes of the dendrograms).
mergeClusters can also be run without merging the cluster, and simply drawing a plot showing the dendrogram along with the estimates of the percentage of non-null features to aid in deciding a cutoff and method. By setting plotInfo="all", all of the estimates of the different methods are displayed simultaneously, while before we only showed the values for the specific mergeMethod we requested.
ce<-mergeClusters(ce,mergeMethod="none",plotInfo="all")
Notice that now if we call nodeMergeInfo, all of the methods now have estimates (except for some methods that didn’t run successfully for this data).
nodeMergeInfo(ce)
## NodeId Contrast isMerged mergeClusterId Storey
## 1 NodeId1 (X2+X5+X4+X7)/4-(X1+X3+X6)/3 NA NA 0.4400905
## 2 NodeId2 X2-(X5+X4+X7)/3 NA NA 0.4058566
## 3 NodeId3 X1-(X3+X6)/2 NA NA 0.3526666
## 4 NodeId4 X3-X6 NA NA 0.2477012
## 5 NodeId5 X5-(X4+X7)/2 NA NA 0.4115151
## 6 NodeId6 X4-X7 NA NA 0.2295940
## PC adjP locfdr MB JC
## 1 0.3780116 0.12137502 NA 0.4041590 NA
## 2 0.3512809 0.09478003 NA 0.3702080 NA
## 3 0.2905322 0.05658509 NA 0.3131985 NA
## 4 0.1886942 0.01938039 NA 0.2138916 NA
## 5 0.3429098 0.03437544 NA 0.3760079 NA
## 6 0.2254791 0.02447305 NA 0.2837742 NA
This means in any future calls to mergeClusters there will be no more need for calculations of per-gene significance, which will speed up the calls if you just want to change the cutoff (all of the methods used the same input of per-gene p-values, so recalculating them each time is computationally inefficient). In practice, the default is calculateAll=TRUE, meaning all methods are calculated unless the user specifically requests otherwise.
Now we can pick a cutoff and rerun mergeClusters. We’ll give it a label to keep it separate from the previous merge clusters run we had made. Note, we can turn off plotting completely by setting plot=FALSE.
ce<-mergeClusters(ce,cutoff=0.05,mergeMethod="adjP",clusterLabel="mergeClusters,v2",plot=FALSE)
ce
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final var_makeConsensus.nVAR
## -----------
## Primary cluster type: mergeClusters
## Primary cluster label: mergeClusters,v2
## Table of clusters (of primary clustering):
## -1 m01 m02 m03 m04
## 6 15 14 13 17
## Total number of clusterings: 46
## Dendrogram run on 'makeConsensus,final' (cluster index: 7)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? Yes
Notice that the nodeMergeInfo has changed, since different nodes were merged, but the estimates per node stay the same.
nodeMergeInfo(ce)
## NodeId Contrast isMerged mergeClusterId Storey
## 1 NodeId1 (X2+X5+X4+X7)/4-(X1+X3+X6)/3 FALSE NA 0.4400905
## 2 NodeId2 X2-(X5+X4+X7)/3 FALSE NA 0.4058566
## 3 NodeId3 X1-(X3+X6)/2 FALSE NA 0.3526666
## 4 NodeId4 X3-X6 TRUE 3 0.2477012
## 5 NodeId5 X5-(X4+X7)/2 TRUE 4 0.4115151
## 6 NodeId6 X4-X7 TRUE NA 0.2295940
## PC adjP locfdr MB JC
## 1 0.3780116 0.12137502 NA 0.4041590 NA
## 2 0.3512809 0.09478003 NA 0.3702080 NA
## 3 0.2905322 0.05658509 NA 0.3131985 NA
## 4 0.1886942 0.01938039 NA 0.2138916 NA
## 5 0.3429098 0.03437544 NA 0.3760079 NA
## 6 0.2254791 0.02447305 NA 0.2837742 NA
If we want to rerun mergeClusters with a different method, we can do that instead.
ce<-mergeClusters(ce,cutoff=0.15,mergeMethod="MB",
clusterLabel="mergeClusters,v3",plot=FALSE)
ce
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final var_makeConsensus.nVAR
## -----------
## Primary cluster type: mergeClusters
## Primary cluster label: mergeClusters,v3
## Table of clusters (of primary clustering):
## -1 m01 m02 m03 m04 m05 m06 m07
## 6 15 14 9 8 5 4 4
## Total number of clusterings: 47
## Dendrogram run on 'makeConsensus,final' (cluster index: 8)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? Yes
We can use plotDendrogram to compare the results. Notice that plotDendrogram can recreate the above plots that were created in the calls to mergeClusters via the argument mergeInfo (of course, this only works after mergeClusters has actually been called so that the information is saved in the ce object).
par(mar=c(1.1,1.1,6.1,2.1))
plotDendrogram(ce,whichClusters=c("mergeClusters,v3","mergeClusters,v2"),mergeInfo="mergeMethod")
Requiring a certain log-fold change
With a large number of cells, it can be overly easy to get significant results, even if the size of the differences is small. Another reasonable constraint is to require the difference between the contrasts to be at least of a certain fold-change for the gene to be counted as different. We allow this option for the merge method adjP. Namely, the proportion significant calculated at each node requires both an adjusted p-value less than 0.05 but also that the estimated \(log_2\) fold-change have an absolute value greater than an amount specified by the argument logFCCutoff.
ce<-mergeClusters(ce,cutoff=0.05,mergeMethod="adjP", logFCcutoff=2,
clusterLabel="mergeClusters,FC1",plot=FALSE)
ce
## class: ClusterExperiment
## dim: 7069 65
## reducedDimNames: PCA
## filterStats: var var_makeConsensus.final var_makeConsensus.nVAR
## -----------
## Primary cluster type: mergeClusters
## Primary cluster label: mergeClusters,FC1
## Table of clusters (of primary clustering):
## -1 m01 m02 m03 m04
## 6 15 14 13 17
## Total number of clusterings: 48
## Dendrogram run on 'makeConsensus,final' (cluster index: 9)
## -----------
## Workflow progress:
## clusterMany run? Yes
## makeConsensus run? Yes
## makeDendrogram run? Yes
## mergeClusters run? Yes
In this case, we can see that it did not make a difference in the merging.
par(mar=c(1.1,1.1,6.1,2.1))
plotDendrogram(ce,whichClusters=c("mergeClusters,FC1","mergeClusters,v3","mergeClusters,v2"),mergeInfo="mergeMethod")
Keeping track of and rerunning elements of the workflow
The commands we have shown above show a workflow which continually saves the results over the previous object, so that additional information just gets added to the existing object.
What happens if some parts of the clustering workflow are re-run? For example, in the above we reran parts of the workflow when we talked about them in more detail, or to experiment with parameter settings.
The workflow commands check for existing clusters of the workflow (based on the clusterTypes of the clusterings). If there exist clusterings from previous runs and such clusterings came from calls that are “downstream” of the requested clustering, then the method will change their clusterTypes value by adding a “.i”, where \(i\) is a numerical index keeping track of replicate calls.
For example, if we rerun ‘makeConsensus’, say with a different parameter choice of the proportion similarity to require, then makeConsensus searches the existing clusterings in the input object. We’ve already seen that any existing makeConsensus results will have their clusterTypes changed from makeConsensus to makeConsensus.x, where \(x\) is the largest such number needed to be greater than any existing makeConsensus.x (after all, you might do this many times!). Their labels will also be updated if they just have the default label, but if the user has given different labels to the clusters those will be preserved.
Moreover, this rerunning of makeConsensus will also effect everything in the analysis that was downstream of it and depended on that call. So since mergeClusters is downstream of makeConsensus in the workflow, currently existing mergeClusters will also get bumped to mergeClusters.x along with makeConsensus. However, clusterMany is upstream of makeConsensus (i.e. you expect there to be existing clusterMany before you run makeConsensus) so nothing will happen to clusterMany.
This is handled internally, and may never be apparent to the user unless they choose whichClusters="all" in a plotting command. Indeed this is one reason to always pick whichClusters="workflow", so that these saved previous versions are not displayed.
However, if the user wants to “go back” to previous versions and make them the current iteration, we have seen that the setToCurrent command will do this (see example in the section on makeDendrogram). setToCurrent follows the same process as described above, only with an existing cluster set to the current part of the pipeline.
Note that there is nothing that governs or protects the clusterTypes values to be of a certain kind. This means that if the user decides to name a clusterTypes of a clustering one of these protected names, that is allowed. However, it could clearly create some havoc if done poorly.
Erasing old clusters You can also choose to have all old versions erased by choosing the options eraseOld=TRUE in the call to clusterMany, makeConsensus,mergeClusters and/or setToCurrent. eraseOld=TRUE in any of these functions will delete ALL past workflow results except for those that are both in the current workflow and “upstream” of the requested command. You can also manually remove clusters with removeClusters.
Finding workflow iterations Sometimes which numbered iteration a particular call is in will not be obvious if there are many calls to the workflow. You may have a mergeClusters.2 cluster but no mergeClusters.1 because of an upstream workflow call in the middle that bumped the iteration value up to 2 without ever making a mergeClusters.1. If you really want to, you can see more about the existing iterations and where they are in the clusterMatrix. “0” refers to the current iteration; otherwise the smaller the iteration number, the earlier it was run.
workflowClusterTable(ce)
## Iteration
## Type 0 1 2 3 4 5 6 7 8
## final 0 0 0 0 0 0 0 0 0
## mergeClusters 1 0 0 1 0 0 1 1 1
## makeConsensus 1 1 1 0 1 1 1 0 0
## clusterMany 36 0 0 0 0 0 0 0 0
Explicit details about every workflow cluster and their index in clusterMatrix is given by workflowClusterDetails:
head(workflowClusterDetails(ce),8)
## index type iteration label
## 1 1 mergeClusters 0 mergeClusters,FC1
## 2 2 mergeClusters 8 mergeClusters,v3
## 3 3 mergeClusters 7 mergeClusters,v2
## 4 4 mergeClusters 6 mergeClusters.6
## 5 5 makeConsensus 6 makeConsensus,nVAR
## 6 6 makeConsensus 5 consensusPCA50
## 7 7 makeConsensus 4 consensusPCA15
## 8 8 mergeClusters 3 mergeClusters.3
A note on the whichCluster argument Many functions take the whichCluster argument for identifying a clustering or clusterings on which to perform an action. These arguments all act similarly across functions, and allow the user to give character arguments. As described above, these can be shortcuts like “workflow”, or they can match either clusterTypes or clusterLabels of the object. It is important to note that matching is first done to clusterTypes, and then if not successful to clusterLabels. Since neither clusterTypes nor clusterLabels is guaranteed to be unique, the user should be careful in how they make the call. And, of course, whichCluster arguments can also take explicit numeric integers that identify the column(s) of the clusterMatrix that should be used.
Designate a Final Clustering
A final protected clusterTypes is “final”. This is not created by any method, but can be set to be the clusterType of a clustering by the user (via the clusterTypes command). Any clustering marked final will be considered one of the workflow values for commands like whichClusters="workflow". However, they will NOT be renamed with “.x” or removed if eraseOld=TRUE. This is a way for a user to ‘save’ a clustering as important/final so it will not be changed internally by any method, yet still have it show up with the “workflow” clustering results. There is no limit to the number of such clusters that are so marked, but the utility of doing so will drop if too many such clusters are chosen.
For best functionality, particularly if a user has determined a single final clustering after completing clustering, a user will probably want to set the primaryClusterIndex to be that of the final cluster and rerun makeDendrogram. This will help in plotting and visualizing. The setToFinal command does this.
Here we will demonstrate marking a cluster as final. We go back to our previous mergeClusters that we found with cutoff=0.05 and mark it as our final clustering. First we need to find which cluster it is. We see from our above call to the workflow functions above, that it is clusterType equal to “mergeClusters.4” and label equal to “mergeClusters,v2”. In our call to setToFinal we will decide to change it’s label as well.
ce<-setToFinal(ce,whichCluster="mergeClusters,v2",
clusterLabel="Final Clustering")
par(mar=plotCMar)
plotClusters(ce,whichClusters="workflow")
Note that because it is labeled as “final” it shows up automatically in “workflow” clusters in our plotClusters plot. It has also been set as our primaryCluster and has the new clusterLabel we gave it in the call to setToFinal.
This didn’t get rid of our undesired mergeClusters result that is most recent. It still shows up as “the” mergeClusters result. This might be undesired. We could remove that “mergeClusters” result with removeClusters. Alternatively, we could manually change the clusterTypes to mergeClusters.x so that it doesn’t show up as current.
A cleaner way to do this would have been to first set the desired cluster (“mergeClusters.4”) to the most current iteration with setToCurrent, which would have bumped up the existing mergeClusters result to be no longer current.
RSEC
RSEC is a single function that follows the entire workflow described above, but makes the choices to set subsample=TRUE and sequential=TRUE to provide more robust clusterings. This removes a number of options from clusterMany, making for a slightly reduced set of arguments. RSEC also implements the makeConsensus, makeDendrogram and mergeClusters steps, again with not all the arguments available to those function to be set by the user, only the most common. Furthermore, the defaults set in RSEC are those we choose for our algorithm, and occassionally vary from stand-alone method. The final output is a ClusterExperiment object as you would get from following the workflow.
We give the following correspondence to help see what arguments of each component are fixed by RSEC, and which are allowed to be set by the user (as well as their correspondence to arguments in the workflow functions).
|
Name of Argument in original function (if different) |
Notes |
|
| clusterMany |
sequential=TRUE |
k0s |
ks |
RSEC only sets ‘k0’, no other k |
| - |
distFunction=NA |
clusterFunction |
|
|
| - |
removeSil=FALSE |
reduceMethod |
|
|
| - |
subsample=TRUE |
nFilterDims |
|
|
| - |
silCutoff=0 |
nReducedDims |
|
|
| - |
|
alphas |
|
|
| - |
|
betas |
|
|
| - |
|
minSizes |
|
|
| - |
|
mainClusterArgs |
|
|
| - |
|
subsampleArgs |
|
|
| - |
|
seqArgs |
|
|
| - |
|
run |
|
|
| - |
|
ncores |
|
|
| - |
|
random.seed |
|
|
| - |
|
isCount |
|
|
| - |
|
transFun |
|
|
| - |
|
isCount |
|
|
| makeConsensus |
propUnassigned = (default) |
consensusProportion |
proportion |
| - |
consensusMinSize |
minSize |
|
|
| makeDendrogram |
filterIgnoresUnassigned=TRUE |
dendroReduce |
reduceMethod |
|
| - |
unassignedSamples= (default) |
dendroNDims |
nDims |
|
| mergeClusters |
plot=FALSE |
mergeMethod |
|
|
| - |
|
mergeCutoff |
cutoff |
|
| - |
|
mergeDEMethod |
DEMethod |
|
| - |
|
mergeLogFCcutoff |
logFCcutoff |
|
Finding Features related to a Clustering
The function getBestFeatures finds features in the data that are strongly differentiated between the clusters of a given clustering. Finding the best features is generally the last step in the workflow, once a final clustering has been decided upon, though as we have seen it is also called internally in mergeClusters to decide between which clusters to merge together.
The function getBestFeatures calls either limma (Smyth 2004, Ritchie et al. (2015)) or edgeR (Robinson, Mccarthy, and Smyth 2010) on input data to determine the gene features most associated with a particular clustering. getBestFeatures picks the primaryCluster of a ClusterExperiment object as the clustering to use to find features. If the standard workflow is followed, this will be the last completed step (usually the result of mergeClusters or manually choosing a final cluster via setToFinal). The primaryCluster can of course be changed by setting primaryClusterIndex to point to a different clustering.
The basic implementation of these functions fits a linear model per feature and tests for the significance of parameters of that linear model, with appropriate adjustment to a negative binomial model in the case of edgeR. The main contribution of getBestFeatures is to interface with limma or edgeR so as to pick appropriate parameters or tests for comparing clusters. Naturally, getBestFeatures also seamlessly works with ClusterExperiment objects to minimize the burden on the user. The output is in the form of topTable or topTags in limma or edgeR respectively, i.e. a data.frame giving the relevant features, the p-value, etc.
Note that getBestFeatures will remove all samples unassigned to a cluster (i.e. -1 or -2), so that these samples will not in anyway influence the DE analysis (see [#unassigned] for more information about unassigned samples).
Types of Significance Tests (Contrasts)
There are several choices of what is the most appropriate test to determine whether a feature is differentially expressed across the clusterings. All of these methods first fit a linear model where the clusters categories of the clustering is the explanatory factor in the model (samples with -1 or -2 are ignored). The methods differ only in what significance tests they then perform, which is controlled by the argument type. By default, getBestFeatures finds significant genes based on a F-test between the clusters (type="F"). This is a very standard test to compare clusters, which is why it is the default, however it may not be the one that gives the best or most specific results. Indeed, in our “Quick Start”, we did not use the \(F\) test, but rather all pair-wise comparisons between the clusters.
The \(F\) test is a test for whether there are any differences in expression between the clusters for a feature. Three other options are available that try to detect instead specific kinds of differences between clusters that might be of greater interest. Specifically, these differences are encoded as “contrasts”, meaning specific types of differences between the means of clusters.
Note that for all of these contrasts, we are making use of all of the data, not just the samples in the particular cluster pairs being compared. This means the variance is estimated with all the samples. Indeed, the same linear model is being used for all of these comparisons.
All Pairwise
The option type="Pairs", which we saw earlier, performs all pair-wise tests between the clusters for each feature, testing for each pair of clusters whether the mean of the feature is different between the two clusters. Here is the example from above using all pairwise comparisons on the results of rsec:
pairsAllTop<-getBestFeatures(rsecFluidigm,contrastType="Pairs",DEMethod="edgeR",p.value=0.05)
dim(pairsAllTop)
## [1] 150 10
head(pairsAllTop)
## IndexInOriginal ContrastName InternalName Contrast Feature logFC
## 1 1465 m01-m02 Cl01-Cl02 Cl01-Cl02 DLK1 15.03569
## 2 3788 m01-m02 Cl01-Cl02 Cl01-Cl02 NNAT -12.95394
## 3 5044 m01-m02 Cl01-Cl02 Cl01-Cl02 RPS4Y1 13.65142
## 4 2291 m01-m02 Cl01-Cl02 Cl01-Cl02 GPC3 13.35216
## 5 4286 m01-m02 Cl01-Cl02 Cl01-Cl02 PLXNA4 -13.74639
## 6 5333 m01-m02 Cl01-Cl02 Cl01-Cl02 SLA -14.39600
## logCPM LR P.Value adj.P.Val
## 1 8.804668 126.60954 2.261671e-29 2.398163e-24
## 2 8.751824 106.60850 5.424014e-25 1.150271e-20
## 3 7.424298 91.39647 1.175859e-21 1.781175e-17
## 4 7.126492 85.56250 2.244924e-20 2.975506e-16
## 5 8.642062 79.38483 5.111709e-19 6.022446e-15
## 6 8.897872 77.52585 1.309969e-18 1.262750e-14
Notice that compared to the quick start guide, we didn’t set the parameter number which is passed to topTable, so we can get out at most 10 significant features for each contrast/comparison (because the default value of number in topTable is 10). Similarly, if we didn’t set a value for p.value, topTable would return the top number genes per contrast, regardless of whether they were all significant or not. These are the defaults of topTable, which we purposefully do not modify, but we urge the user to read the documentation of topTable carefully to understand what is being asked for. In the QuickStart, we set number=NROW(rsecFluidigm) to make sure we got all significant genes.
In addition to the columns provided by topTable, the column “Contrast” tells us what pairwise contrast the result is from. “Cl01-Cl02” means a comparison of cluster 1 and cluster 2 (note that these refer to the cluster ids, not any name they might have). The column “IndexInOriginal” gives the index of the gene to the original input data matrix, namely assay(ce). The other columns are given by topTable (with the column “Feature” renamed – it is usually “ProbeID” in limma).
One Against All
The choice type="OneAgainsAll" performs a comparison of a cluster against the mean of all of the other clusters.
best1vsAll<-getBestFeatures(rsecFluidigm,contrastType="OneAgainstAll",DEMethod="edgeR",p.value=0.05,number=NROW(rsecFluidigm))
head(best1vsAll)
## IndexInOriginal ContrastName InternalName
## 1 1465 m01 Cl01
## 2 3788 m01 Cl01
## 3 5044 m01 Cl01
## 4 2291 m01 Cl01
## 5 1640 m01 Cl01
## 6 3985 m01 Cl01
## Contrast Feature logFC logCPM LR
## 1 Cl01-(Cl02+Cl03+Cl04+Cl05+Cl06)/5 DLK1 14.61955 8.804668 143.38432
## 2 Cl01-(Cl02+Cl03+Cl04+Cl05+Cl06)/5 NNAT -13.88048 8.751824 117.35307
## 3 Cl01-(Cl02+Cl03+Cl04+Cl05+Cl06)/5 RPS4Y1 13.23520 7.424298 93.85408
## 4 Cl01-(Cl02+Cl03+Cl04+Cl05+Cl06)/5 GPC3 12.93593 7.126492 86.97279
## 5 Cl01-(Cl02+Cl03+Cl04+Cl05+Cl06)/5 EFNA5 13.49902 8.430487 74.42540
## 6 Cl01-(Cl02+Cl03+Cl04+Cl05+Cl06)/5 OTX2 12.52104 6.714253 68.92582
## P.Value adj.P.Val
## 1 4.843968e-33 2.054521e-28
## 2 2.402547e-27 5.095081e-23
## 3 3.396636e-22 4.802164e-18
## 4 1.100245e-20 1.166645e-16
## 5 6.297363e-18 5.341927e-14
## 6 1.022376e-16 7.227176e-13
Notice that now there is both a “Contrast” and a “ContrastName” column, unlike with the pairs comparison. Like before, “Contrast” gives an explicit definition of what is the comparisons, in the form of “(Cl02+Cl03+Cl04+Cl05+Cl06)/5-Cl01”, meaning the mean of the means of clusters 2-6 is compared to the mean of cluster1. Note that the contrasts here are always written in terms of the internal (numeric) cluster id, with an “Cl” in front of the number and a ‘0’ to make the number 2 digits. “ContrastName” interprets this into a more usable name, namely that this contrast can be easily identified as a test of “Cl01” (cluster 1).
We can plot the contrasts with a heatmap for these results. Here we notice that the color next to the gene group matches the cluster that the contrast matches.
plotContrastHeatmap(rsecFluidigm,signifTable=best1vsAll,nBlankLines=10, whichCluster="primary")
Dendrogram
The option type="Dendro" is more complex; it assumes that there is a hierarchy of the clusters (created by makeDendrogram and stored in the ClusterExperiment object). Then for each node of the dendrogram, getBestFeatures defines a contrast or comparison of the mean expression between the daughter nodes.
bestDendro<-getBestFeatures(rsecFluidigm,contrastType="Dendro",DEMethod="edgeR",p.value=0.05,number=NROW(rsecFluidigm))
head(bestDendro)
## IndexInOriginal ContrastName InternalName Contrast
## 1 1284 NodeId1 NodeId1 (X5+X1+X4)/3-(X6+X2+X3)/3
## 2 5211 NodeId1 NodeId1 (X5+X1+X4)/3-(X6+X2+X3)/3
## 3 4285 NodeId1 NodeId1 (X5+X1+X4)/3-(X6+X2+X3)/3
## 4 5333 NodeId1 NodeId1 (X5+X1+X4)/3-(X6+X2+X3)/3
## 5 2325 NodeId1 NodeId1 (X5+X1+X4)/3-(X6+X2+X3)/3
## 6 3724 NodeId1 NodeId1 (X5+X1+X4)/3-(X6+X2+X3)/3
## Feature logFC logCPM LR P.Value adj.P.Val
## 1 CXADR -7.009895 10.907220 45.53894 1.496340e-11 8.814688e-08
## 2 SEMA3C -10.427061 8.749876 41.86941 9.757713e-11 3.633642e-07
## 3 PLXNA2 -8.469656 8.736883 41.45378 1.206908e-10 3.633642e-07
## 4 SLA -9.949941 8.897872 41.41093 1.233660e-10 3.633642e-07
## 5 GRIA2 -9.834170 8.238138 39.66490 3.014962e-10 8.197217e-07
## 6 NEUROD6 -10.819017 7.752301 39.39243 3.466384e-10 8.751381e-07
Again, there is both a “ContrastName” and “Contrast” column, as well as a “InternalName” column. The “Contrast” column identifies which clusters ids were on each side of the node (and hence commpared). “InternalName” is the internal name of the node, determined internally during makeDendrogram, while “ContrastName” is the name of the node, which might have been set by the user (for information about node names, and how to set the node names see on the (internal structure of the dendrogram](#dendrostructure))
levels((bestDendro)$Contrast)
## [1] "(X5+X1+X4)/3-(X6+X2+X3)/3" "X5-(X1+X4)/2"
## [3] "X6-(X2+X3)/2" "X2-X3"
## [5] "X1-X4"
We can look at the results again with plotContrastHeatmap.
plotContrastHeatmap(rsecFluidigm,signifTable=bestDendro,nBlankLines=10)
We can plot the dendrogram to help make sense of which contrasts go with which nodes and choose to show the node names with show.node.label=TRUE (plotDendrogram calls plot.phylo from the ape package and can take as imput those arguments like show.node.label).
plotDendrogram(rsecFluidigm,show.node.label=TRUE,whichClusters=c("makeConsensus","mergeClusters"),leaf="samples",plotType="colorblock")
DE Analysis for count and other RNASeq data
The getBestFeatures method for ClusterExperiment objects has an argument DEMethod to determine what kind of DE method should be run. The options are limma, limma-voom and edgeR. The last two options assume that assay(x) are counts.
limma In this case, the data is assumed to be continous and roughly normal and the limma DE method is performed on transformData(x), i.e. the data after transformation of the data with the transformation stored in the ClusterExperiment object.
limma-voom refers to calling limma with the voom(Law et al. 2014) correction which uses the normal linear model of limma but deals with the mean-variance relationship that is found with count data. This means that the differential expression analysis is done on \(log_2(x+0.5)\). This is regardless of what transformation is stored in the ClusterExperiment object! The voom call within getBestFeatures sets normalize.method = "none" in the call to voom. Unlike edgeR or DESeq, the voom correction does not explicitly require a count matrix, and therefore it has been proposed that it can be used on FPKM or TPM entries, or data normalized via RUV. However, the authors of the package do not recommend using voom on anything other than counts, see e.g. this discussion.
edgeR Performs a likelihood-ratio test (glmLRT function in edgeR (Robinson, Mccarthy, and Smyth 2010)) based on a negative binomial distribution and a empirical bayes estimation of the dispersion.
edgeR with zero-inflated weights Weights can be provided to getBestFeatures, in which case the LRT is performed using the function glmWeightedF in the zinbwave package following the work of (Van den Berge et al. 2018). The best way to do this is to save the weights in an assay entitled weights. Here is an example of mock code:
assay(rsecFluidigm,"weights")<- myweights
If the initial SummarizedExperiment object is set up this way, then the functions getBestFeatures, mergeClusters , and RSEC will all automatically look for such an assay in order to use these weights, if DEMethod="edgeR". Indeed for RSEC this is the only way to get weights used – unlike getBestFeatures and mergeClusters, RSEC doesn’t give a way for the user to make choices about the weights (this is to simplify the number of parameters). For getBestFeatures and mergeClusters you can manually set the argument weights to be NULL to force the functions to NOT use the weights stored here (and the standard edgeR routine is followed instead) or alternatively set weights to be another assay name or even a matrix of weights.
Normalization Factors Both limma-voom and edgeR calls first set up a DGEList object which is then given to either the voom function in the limma package or the estimateDisp function of edgeR. The argument counts to the DGEList function is given by the data in the assay, but you can pass other arguments to the call to DGEList by giving them in a list format to the argument dgeArgs of getBestFeatures (or the other functions that call getBestFeatures). In particular, you can pass arguments such as norm.factors or lib.size to specify normalization factors, which will then be used by the voom/edgeR commands.
Piping into other DE routines
Ultimately, for many settings, the user may prefer to use other techniques for differential expression analysis or have more control over certain aspects of it. The function clusterContrasts may be called by the user to get the contrasts that are defined within getBestFeatures (e.g. dendrogram contrasts or pairwise contrasts). These contrasts, which are in the format needed for limma or edgeR can be piped into programs that allow for contrasts in their linear models for mRNA-Seq; they can also be chosen to be returned in the formated needed by MAST (Finak et al. 2015) for single-cell sequencing by settting outputType="MAST".
Similarly, more complicated normalizations, like RUV (Gagnon-Bartsch and Speed 2011), adjust each gene individually for unwanted batch or other variation within the linear model. In this case, a matrix \(W\) that describes this variation should be included in the linear model. Again, this can be done in other programs, using the contrasts provided by clusterContrasts in combination with \(W\).
Multiple Testing adjustments
The user should be careful about questions of multiple comparisons when so many contrasts are being performed on each feature; the default is to correct across all of these tests (see the help of getBestFeatures and the argument contrastAdj for more). As noted in the introduction, p-values created in this way are reusing the data (since the data was also used for creating the clusters) and hence should not be considered valid p-values regardless.
As mentioned, getBestFeatures accepts arguments to limma’s function topTable (or topTags for edgeR) to decide which genes should be returned (and in what order). In particular, we can set an adjusted p-value cutoff for each contrast, and set number to control the number of genes returned for each contrast. By setting number to be the length of all genes, and p.value=0.05, we can return all genes for each contrast that have adjusted p-values less than 0.05. All of the arguments to topTable regarding what results are returned and in what order can be given by the user at the call to getBestFeatures.
