Abstract
Background
The use of correlation networks is widespread in the analysis of gene expression and proteomics data, even though it is known that correlations not only confound direct and indirect associations but also provide no means to distinguish between cause and effect. For "causal" analysis typically the inference of a directed graphical model is required. However, this is rather difficult due to the curse of dimensionality.
Results
We propose a simple heuristic for the statistical learning of a highdimensional "causal" network. The method first converts a correlation network into a partial correlation graph. Subsequently, a partial ordering of the nodes is established by multiple testing of the logratio of standardized partial variances. This allows identifying a directed acyclic causal network as a subgraph of the partial correlation network. We illustrate the approach by analyzing a large Arabidopsis thaliana expression data set.
Conclusion
The proposed approach is a heuristic algorithm that is based on a number of approximations, such as substituting lower order partial correlations by full order partial correlations. Nevertheless, for small samples and for sparse networks the algorithm not only yield sensible first order approximations of the causal structure in highdimensional genomic data but is also computationally highly efficient.
Availability and Requirements
The method is implemented in the "GeneNet" R package (version 1.2.0), available from CRAN and from http://strimmerlab.org/software/genets/ webcite. The software includes an R script for reproducing the network analysis of the Arabidopsis thaliana data.
Background
Correlation networks are widely used to explore and visualize highdimensional data, for instance in finance [13], ecology [4], gene expression analysis [5,6], or metabolomics [7]. Their popularity is owed to a large extent to the ease with which a correlation network can be constructed, as this requires only two simple steps: i) the computation of all pairwise correlations for the investigated variables, and ii) a thresholding or filtering procedure [8] to identify significant correlations, and hence edges, of the network.
However, for shedding light on the causal processes underlying the observed data, correlation networks are only of limited use. This is due to the fact that correlations not only confound direct and indirect associations but also provide no means to distinguish between response variables and covariates (and thus between cause and effect).
Therefore, causal analysis requires tools different from correlation networks: much of the work in this area has focused on Bayesian networks [9] or related regression models such as systems of recursive equations [10,11] or influence diagrams [12]. All of these models have in common that they describe causal relations by an underlying directed acyclic graph (DAG).
There already exist numerous methods for learning DAGs from observational data – see for instance the summarizing review in [13] and the references therein. However, with few exceptions [e.g., the PC algorithm, [14,15]] virtually all of these methods have been devised for comparatively small numbers of variables and with large sample size in mind. For instance, the numerical example of the recently proposed algorithm described in [16] uses n = 10,000 observations for p = 7 variables. Unfortunately, the data that would be most interesting to explore with causal methods, namely those commonly visualized by correlation networks (see above), have completely different characteristics, in particular they are likely of high dimension.
In this paper we follow [15] and focus on modeling largescale linear recursive systems. Specifically, we present a simple discovery algorithm that enables the inference of causal relations from small sampled data and for large numbers of variables. It proceeds in two steps as follows:
• First, the correlation network is transformed into a partial correlation network, which is essentially an undirected graph that displays the direct linear associations only. This type of network model is also known under the names of graphical Gaussian model (GGM), concentration graph, covariance selection graph, conditional independence graph (CIG), or Markov random field. Note that there is a simple relationship between correlation and partial correlation. Moreover, in recent years there has been much progress with regard to statistical methodology for learning largescale partial correlation graphs from small samples [e.g., [1722]]. Here we employ the approach described in [20].
• Second, the undirected GGM is converted into a partially directed graph. This is done by estimating a pairwise ordering of the nodes from the data using multiple testing of the logratios of standardized partial variances, and by subsequent projection of this partial ordering onto the GGM. The inferred causal network is the subgraph containing all the directed edges.
Note that this algorithm is similar to the PC algorithm in that edges are being removed from the independence graph to obtain the underlying DAG. However, our criterion for eliminating an edge is distinctly different from that of the PC algorithm.
The remainder of the paper is organized as follows. First, we describe the methodology. Second we consider its statistical interpretation and further properties. Subsequently, we illustrate the approach by analyzing an 800 gene data set from a largescale Arabidopsis thaliana gene expression experiment. Finally, we conclude with some discussion of the method, commenting also on the limitations of the approach.
Methods
Theoretical basis
Consider a linear regression with Y as response and X_{1}, ..., X_{k}, ..., X_{K }as covariates. We assume that X_{k }and Y are random variables with known variances var(Y) and var(X_{k}) and with covariance cov(Y, X_{k}). The best linear predictor of Y in terms of the X_{k }that minimizes the MSE of ∑_{k }β_{k}X_{k } Y is given by [e.g. ref. [23], p. 206]
where
The partial correlation is the correlation that remains between two variables if the effect of the other variables has been regressed away. Likewise, the partial variance is the variance that remains if the influences of all other variables are taken into account. Table 1 lists the definitions and formulas for the computation of these quantities (note that in our notation a tilde on top of a symbol indicates ''partial'').
Table 1. Formulas for computing partial variances and partial correlations
From Equation 1 it is immediately clear that the complete linear system and thus all
We emphasize that Equation 1 has a direct relation with the usual ordinary least squares
(OLS) estimator for the regression coefficient. This is recovered if the empirical
covariance matrix is plugged into Equation 1. However, note that Equation 1 also remains
valid if other estimates of the covariance are used, such as penalized or shrinkage
estimators (note that there is no hat on
For the following it is important that Equation 1 can be further rewritten by introducing
a scale factor. Specifically, by abbreviating the standardized partial variance
Note that SPV_{y }and SPV_{k }take on values from 0 to 1. All three factors have an immediate and intuitive interpretation:
The product
In this context it is also helpful to recall the diverse statistical interpretations of SPV:
• SPV is the proportion of variance that remains (unexplained) after regressing against all other variables.
• For the OLS estimator SPV is equal to 1  R^{2}, where R is the usual coefficient of determination.
• SPV is the inverse of the diagonal of the inverse of the correlation matrix. Thus, if there is no correlation (unit diagonal correlation matrix) the partial variance equals the variance, and hence SPV = 1.
• SPV may also be estimated by 1/VIF, where VIF is the usual variance inflation factor [cf. [26]].
Heuristic algorithm for discovering approximate causal networks
The above decomposition (Equation 2) suggests the following simple strategy for statistical
learning of causal networks. First, by multiple testing of
In more detail, we propose the following fivestep algorithm:
1. First, it is essential to determine an accurate and positive definite estimate R of the correlation matrix. Only if the sample size is large with many more observations than variables (n > > p) the usual empirical correlation estimate will be suitable. In all other instances, the use of a regularized estimator is absolutely vital (e.g., the Steintype shrinkage estimator of [20]) in order to improve efficiency and to guarantee positive definiteness. In addition, if the samples are longitudinal it may be necessary to adjust for autocorrelation [27].
2. From the estimated correlations we compute the partial variances and correlations
(see Table 1), and from those in turn plugin estimates of the factors
3. Subsequently, we infer the partial correlation graph following the algorithm described
in [19]. Essentially, we perform multiple testing of all partial correlation coefficients
4. In a similar fashion we then conduct multiple testing of all log(
Assuming that most z belong to the null model, i.e. that most edges are undirected, it is possible to infer
nonparametrically the alternative distribution f_{A }(z), the proportion η_{0}, as well as the variance parameter θ – for an algorithm see [28]. From the resulting densities and distribution functions local and tailareabased
false discovery rates for the test log(
5. Finally, a partially directed network is constructed as follows. All edges in the
correlation graph with significant log(
Results and discussion
Interpretation of the resulting graph
The above algorithm returns a partially directed partial correlation graph, whose directed edges form a causal network.
This procedure can be motivated by the following connection between partial correlation
graph and a system of linear equations, where each node is in turn taken as a response
variable and regressed against all other remaining nodes. In this setting the partial
correlation coefficient is the geometric mean of
[see also equation 16 of ref. [20]]. In this light, an undirected edge between two nodes A and B in a partial correlation
graph may also be interpreted as bidirected edge, in the sense that A influences B
and vice versa in the underlying system of regression. Therefore, the test
Reconstruction efficiency and approximations underlying the algorithm
Topology of the network
The proposed algorithm is an extension of the GGM inference approach of [19,20]. Its accuracy of correctly recovering the topology of the partial correlation graph has been established, e.g., in [30].
However, it is well known that a directed Bayesian network and the corresponding undirected graph are not necessarily topologically identical: in the undirected graph for computing the partial correlations one conditions on all other nodes whereas in the directed graph one conditions only on a subset of nodes, in order to avoid conditioning "on the future" (i.e. on the dependent nodes). Therefore, it is critical to evaluate to what extent full order partial correlations are reasonable approximations for lower order partial correlations. This has already been investigated intensively by [31] who showed that in certain situations (sparse graphs, faithfulness assumption etc.) lower order partial correlations may be used as approximate substitute of full conditional correlations. Therefore, in the proposed algorithm we adopt the very same argument but apply it in the different direction, i.e. we approximate lower order partial correlation by full order partial correlation.
Node ordering
A second approximation implicit in our algorithm concerns the determination of the ordering of the nodes, which is done by multiple testing of pairwise ratios of standardized partial variances. We have conducted a number of numerical simulations (data not shown) that indicate that for randomly simulated DAGs the ordering of the nodes is indeed well reflected in the partial variances, as expected.
However, from variable selection in linear models it is also known that the partial
variance (or the related R^{2}) may not always be a reliable indicator for variable importance. Nevertheless, the
partial ordering of nodes according to SPV and the implicit model selection in the
underlying regressions is a very different procedure in comparison to the standard
variable selection approaches, in which the increase or decrease of the R^{2 }is taken as indicator of whether or not a variable is to be included, or a decomposition
of R^{2 }is sought [for a review see, e.g., [32]]. The distinctive feature of our procedure is that by performing all tests log(
It is also noteworthy that, as we impose directionality from the less well explained variable (large SPV, "exogenous", "independent") to the one with relatively lower SPV (well explained, "endogenous", "dependent" variable), we effectively choose the direction with the relatively smaller regression coefficient (conditional that the corresponding partial correlation is also significant).
Further properties of the heuristic algorithm and of the resulting graphs
The simple heuristic network discovery algorithm exhibits a number of further properties worth noting:
1. The estimated partially directed network cannot contain any (partially) directed cycles. For instance, it is not possible for a graph to contain a pattern such as A → B → A. This example would imply SPV_{A }> SPV_{B }> SPV_{A}, which is a contradiction. As a consequence, the subgraph containing the directed edges only is also acyclic (and hence a DAG).
2. The assignment of directionality is transitive. If there is a directed edge from A to B and from B to C then there must also be a directed edge from A to C. Note however, that actual inclusion of a directed edge into the causal network is conditional on a nonzero partial correlation coefficient.
3. As the algorithm relies on correlations as input, causal processes that produce the same correlation matrix lead to the same inferred graph, and hence are indistinguishable. The existence of such equivalence classes is well known for SEMs [33] and also for Bayesian belief networks [34].
4. The proposed algorithm is scaleinvariant by construction. Hence, a (linear) change in any of units of the data has no effect on the overall estimated partially directed network, and the implied causal relations.
5. We emphasize that the partially directed network is not the chain graph representing the equivalence class of the causal network that is obtained by considering only its directed edges – see [34].
6. The computational complexity of the algorithm is O(p^{3}). Hence, it is no more expensive than computing the partial correlation graph, and thus allows for estimation of networks containing in the order of thousands and more nodes.
Analysis of a plant expression data set
To illustrate our algorithm for discovering causal structure, we applied the approach to a real world data example. Specifically, we reanalyzed expression time series resulting from an experiment investigating the impact of the diurnal cycle on the starch metabolism of Arabidopsis thaliana [35]. This is the same data set we used in a sister paper concerning the estimation of a vector autoregressive model [36].
The data are gene expression time series measurements collected at 11 different time points (0, 1, 2, 4, 8, 12, 13, 14, 16, 20, and 24 hours after the start of the experiment). The corresponding calibrated signal intensities for 22,814 genes/probe sets and for two biological replicates are available from the NASCArrays repository, experiment no. 60 [37]. After logtransforming the data we filtered out all genes containing missing values and whose maximum signal intensity value was lower than 5 on a logbase 2 scale. Subsequently, we applied the periodicity test of [38] to identify the probes associated with the daynight cycle. As a result, a subset of 800 genes remained for further analysis.
In order to estimate the correlation matrix for the 800 genes described by the data set we employed the dynamical correlation shrinkage estimator of [39] as this takes account of the autocorrelation. The corresponding correlation graph is displayed in Figure 1. It shows the 150 edges with the largest absolute values of correlation. This graph is very hard to interpret, the branches do not have any immediate or intuitive meaning (a complete annotation of the nodes can be found along with the dataset itself in the R package "GeneNet" [40]). For instance, there are no hubs as typically observed in biological networks [41,42].
Figure 1. Correlation network inferred from the Arabidopsis thaliana data. The solid and dotted lines indicate positive and negative correlation coefficients, respectively, and the line intensity denotes their strength. The network displays the 150 edges with the largest absolute correlation. For annotation of the nodes in this graph see the electronic information contained in the R package "GeneNet" [40] and the original data paper [35].
This is in great contrast to the partially directed partial correlation graph. For
this specific data set, by multiple testing of the factor
Figure 2. Distribution of log
To construct the network, we projected upon the significant edges (factor
The resulting partially causal network is shown in Figure 3. For reasons of clarity we show only the subnetwork containing the 150 most significant edges, which connect 107 nodes. This graph exhibits a clear "hub" connectivity structure (nodes filled with red color). A prominent example for this is node 570, others are 81, 558, 783 and a few more genes. We see that many of the hub nodes have mostly outgoing arcs, which is indicative for key regulatory genes. This applies, e.g., to node 570, an AP2 transcription factor, or to node 81, a gene involved in DNAdirected RNA polymerase. An interesting aspect of the partially causal network is the web of highly connected genes (colored yellow in the lower right corner of Figure 3), which we hypothesize to constitute some form of a functional module. In this module, it is not possible to determine any directions, which could be due to complex interactions among the nodes of the module. Node 627 is another hub in the network that connects the functional module with the rest of the network and which according to the annotation of [35] encodes a protein of unknown function.
Figure 3. Partially causal network inferred from the Arabidopsis thaliana data by the method introduced in this paper – note the difference to the correlation
network of Figure 1. The topology of the partially causal network is identical to
that of a partial correlation graph (GGM, CIG). However, edges with significant directionality
(as indicated by a factor
We also see that the partially directed network contains both directed and undirected nodes. This is a distinct advantage of the present approach. Unlike, e.g., a vector autoregressive model [36], it does not force directions onto the edges.
Finally, in order to investigate the stability of the inferred partial causal network, we randomly removed data points from the sample, and repeatedly reconstructed the network from the reduced data set. In all cases the general topological structure of the network remained intact, which indicates that this is a signal inherent in the data. This is also confirmed by the analysis using vector autoregressions [36].
Conclusion
Methods for exploring causal structures in highdimensional data are growing in importance, particularly in the study of complex biological, medical and financial systems. As a first (and often only) analysis step these data are explored using correlation networks.
Here we have suggested a simple heuristic algorithm that, starting from a (positive definite) correlation matrix, infers a partially directed network that in turn allows generating causal hypotheses of how the data were generated. Our approach is approximate, but it allows analysis of highdimensional small sampled data, and its computational complexity is very modest. Thus, our heuristic is likely to be applicable whenever a correlation network is computed, and therefore is suitable for screening largescale data set for causal structure.
Nevertheless, there a several lines along which this method could be extended. For instance, nonlinear effects could be accounted for by employing entropy criteria, or by using higher order moments [16]. Furthermore, more sophisticated algorithms may be used to enhance the approximation of lower order partial correlations or the inference of the ordering of the nodes. However, ultimately this would lead to a method similar to the PC algorithm [14,15].
Note that the PC algorithm is more refined than our algorithm, primarily due to additional steps that aim at removing spurious edges (i.e. those edges that are induced between otherwise uncorrelated parent nodes by conditioning on a common child node). However, these iterative refinements may be very time consuming, in particular for highdimensional graphs.
In contrast, our procedure is noniterative and therefore both computationally and algorithmically (nearly) as simple as a correlation network. Nevertheless, it still enables the discovery of partially directed processes underlying the data.
In summary, we recommend our approach as a procedure for exploratory screening for causal mechanisms. Subsequently, the resulting hypotheses may then form the basis for more refined analyzes, such as full Bayesian network modeling.
Authors' contributions
Both authors participated in the development of the methodology and wrote the manuscript. RO carried out all analyzes. All authors approved of the final version of the manuscript.
Availability and requirements
The method is implemented in the "GeneNet" R package (version 1.2.0), available from CRAN and from http://strimmerlab.org/software/genets/ webcite. The software includes an R script for reproducing the network analysis of the Arabidopsis thaliana data.
Acknowledgements
This work was in part supported by an "Emmy Noether" excellence grant of the Deutsche Forschungsgemeinschaft (to K.S.).
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