A temporal precedence based clustering method for gene expression microarray data
- Ritesh Krishna^{1},
- Chang-Tsun Li^{1}Email author and
- Vicky Buchanan-Wollaston^{2}
https://doi.org/10.1186/1471-2105-11-68
© Krishna et al; licensee BioMed Central Ltd. 2010
Received: 12 August 2009
Accepted: 30 January 2010
Published: 30 January 2010
Abstract
Background
Time-course microarray experiments can produce useful data which can help in understanding the underlying dynamics of the system. Clustering is an important stage in microarray data analysis where the data is grouped together according to certain characteristics. The majority of clustering techniques are based on distance or visual similarity measures which may not be suitable for clustering of temporal microarray data where the sequential nature of time is important. We present a Granger causality based technique to cluster temporal microarray gene expression data, which measures the interdependence between two time-series by statistically testing if one time-series can be used for forecasting the other time-series or not.
Results
A gene-association matrix is constructed by testing temporal relationships between pairs of genes using the Granger causality test. The association matrix is further analyzed using a graph-theoretic technique to detect highly connected components representing interesting biological modules. We test our approach on synthesized datasets and real biological datasets obtained for Arabidopsis thaliana. We show the effectiveness of our approach by analyzing the results using the existing biological literature. We also report interesting structural properties of the association network commonly desired in any biological system.
Conclusions
Our experiments on synthesized and real microarray datasets show that our approach produces encouraging results. The method is simple in implementation and is statistically traceable at each step. The method can produce sets of functionally related genes which can be further used for reverse-engineering of gene circuits.
Keywords
Background
Microarrays allow simultaneous measurement of thousands of genes in a short span of time. This approach provides abundant opportunities for scientists to detect and experimentally validate the hypothesis that the data might be generating. Microarray experiments have traditionally focused on measurement of gene expressions at a single time point and are increasingly being applied to measure expression-levels across multiple time points. Such time-course measurements can help in gaining insights into the dynamics of gene interactions [1–3]. The computational analysis of temporal microarray data requires three distinct stages to be performed before some meaningful hypothesis from data can be derived. The first stage is the normalization stage where data is cleaned from the effects of unwanted experimental biases [4, 5]. The second stage requires the grouping of data based on certain features which helps in reduction of data dimensions. The third and final stage is the inference of relationship between various genes of interest and understanding the functioning of smaller subsystems which comprise together to make a bigger system. Though these three stages have an ordered sequence of execution, the computational methods applied at these stages need not be dependent on each other. The normalization method solely relies on the experimental design of the microarray experiment [5, 6]. The clustering step can be performed using point-based, model-based or feature based grouping of data [7] depending on the hypothesis adopted by the practitioner. The final stage of relationship inference between genes is restricted to the sets of selected genes which can be studied as a system of bivariate or multivariate causal interactions. Keeping in mind, the final goal of microarray data analysis being identification of interactions between genes at the third level, the quest for this goal should ideally start when the data is being grouped together at the clustering stage. One of the ultimate goals of all gene clustering algorithms is to discover the underlying gene pathways representing the biological processes. Genes that are lying in the same pathway are often activated or depressed simultaneously or sequentially upon receiving stimuli. The biological signal is typically transmitted through intermediate gene interactions due to physical or chemical activities. The simultaneous or sequential activation, or depression, is delineated by the underlying network connection patterns. In this paper, we present a novel approach for clustering of temporal microarray data based on the notion of temporal interaction between the genes. The temporal recording of gene expressions provides an excellent opportunity to view the gene profiles with respect to time and helps in understanding the underlying causal processes driving the behavior of the genes and the system in turn. Like any dynamical system, in a system with a temporal expression profile, time plays a crucial role in the way the system behaves. The primary hypothesis behind the approach presented in this paper is: the observed effect on any gene is due to some cause propagated over time. The observed expression of a gene could be due to the effect of other genes present in the system which may be activating or inhibiting the gene under observation with different time-lags. In other words, we perceive the system as a set of interacting entities, where each entity is a stochastic process and the interactions between them are temporal activities taking place between a pair of processes.
A system with such behavior is a widely accepted concept in Economics and Neuroscience. Granger [8] proposed a method to evaluate the influence of one time series on the other time series. Granger causality has recently been introduced in bioinformatics [9–12] to reverse-engineer gene circuits from microarray data. We will utilize Granger causality in conjunction with a graph-theoretic method to build an association matrix for the genes and detect the functional modules present in the data. A functional module can be defined as a separate substructure of a network having a group of genes or their products that are related by physical or genetic interactions. In graph-theoretic sense, a functional module can be represented by highly connected regions in a network, where the functions are predicted using connections in a graph based on the assumption that genes which lie close to one another are more likely to have similar functions or constitute gene complexes [13, 14]. We will also analyze that how the association network obtained by us has certain architectural properties desired from biological networks [15] which distinguishes it from a randomly generated network.
Related Work
- 1.
Point-wise distance based methods - group genes by minimizing an objective function based on a distance measure computed between gene pairs. The distance measure could be Euclidean distance, mutual information, correlation or its respective variants [16], etc. The point-wise methods can be further classified into two classes: (a) partitioning, and (b) hierarchical. Among partitioning methods, k-means [17] and self-organizing maps (SOM) [18] are widely used approaches. Hierarchical methods on the other hand create a hierarchy of relative distances and place multinomial points along a one-dimensional axis based on the relative distance between points. A typical representation of results obtained from hierarchy based methods is in the form of a dendrogram [19]. Point-wise distance based approaches are the most widely used clustering techniques for gene expression data due to their computational and conceptual simplicity. These methods are also popular due to their implementation in the large number of software packages designed for analysis of gene expression data. Some biological case studies using point-wise methods for clustering gene expression data can be found in [20–22].
- 2.
Feature based clustering methods - aim at detecting salient features and local or global shape characteristics of the expression profiles. As opposed to a distance based similarity measure, looking for general shape among the gene profiles can uncover more intricate relationships, such as time shifts and inversion in expression profiles. Ji and Tan [23] proposed a time-lagged based cluster identification technique which relies on the directional change of profiles across consecutive time points. Edge detection method by Chen et al. [24] sums the number of edges of two gene expression curves where edges have the same direction within a time lag to generate a score. Directional changes were also used to compute the slope of expression values in Event method by Kwon et al. [25] to cluster the gene profiles. Some of the feature based clustering methods transform the raw expression data to symbols which are further analyzed to detect similarity between profiles [26, 27]. Dominant Spectral Component Method by Yeung et al. [28] decomposes temporal expression sequences into spectral components using the autoregressive modeling technique to measure gene-gene relationship to form clusters. Graph-theoretic approaches studying the nature, properties, structure of the graph where the genes represent the nodes and the arcs representing association between genes also come under feature based clustering methods. Graph spectral clustering [29] and minimal spanning tree methods [30, 31] are other well-known feature based clustering methods.
- 3.
Model based clustering methods - shift the similarity emphasis from the data to the unknown model that describes the data. Such methods are based on statistical mixture models which assume that data is generated by a finite mixture of underlying probability distributions, with each component corresponding to a distinct cluster [32–35]. Model based clustering relies on the fundamental assumption that the observed expression profiles are clustered in functional space based on their characteristics. The focus of this approach is in functional decomposition of data, rather than the decomposition of raw data. The computational approach in model based clustering methods is based on maximizing the likelihood of data points. Expectation-maximization (EM) is a popular model based clustering approach to estimate unknown parameters (mean and standard deviation in case of Gaussian distribution) of underlying probability distribution for each cluster in order to maximize the likelihood of the observed expression profiles [36]. Based on similar lines as EM algorithm, Schliep et al. [37, 38] suggested gene clustering based on a mixture of Hidden Markov Model (HMM). Along the similar thoughts that a time-course gene dataset is a set of time series generated by stochastic processes, Ramoni et al. [39] suggested the use of autoregressive representation for each stochastic process defining a cluster. This method relies on regression and groups together genes whose dynamics can be expressed with roughly the same auto-regressive equation. Bar-Joseph et al. [40] presented a clustering algorithm that uses splines to cluster the continuous representation of time series expression data. In some cases, prior knowledge has been used to fit the models to the expression profiles. For example, Zhao et al. [41] and Lu et al. [42] have used sinusoids to identify yeast genes with cyclic behaviour. Moller-Levet et al. [43] presented a method based on a predefined comprehensive set of profiles to cluster genes according to their match with respective profiles.
The method proposed in this paper for clustering of temporal gene expression data takes advantage of the essential behaviour of the Granger causality test, which determines if one time-series is useful in forecasting the other time-series or not. The network obtained after applying the Granger causality test is representative of the association between gene-pairs which pass the test. In order to detect the potential functionally related genes, we use a graph theoretical technique to detect dense regions in the association network. Our approach shows that the detection of dense regions in association with Granger causality test plays an equally important role in the proposed clustering technique. The method is tested using both synthetic as well as real datasets obtained to monitor senescence in Arabidopsis Thaliana. To the best of our knowledge, this is a new approach in clustering of temporal gene-expression data which can be used for automated grouping of interesting genes from a large dataset.
Results and Discussion
Experiments with Synthetic Datasets
We test our method on three sets of synthetic multivariate datasets. Each set represents a collection of stochastic processes in the form of time-series. We construct each set in such a way that the processes belonging to the set are interdependent, whereas the sets themselves are disjoint from each other.
In the above datasets, ϵ_{ i }~ N(0,1) represents the uncorrelated random error associated with each process. In Dataset 1, x_{1} is the driving force for x_{2}, x_{3} and x_{4} with time lags 2,3 and 2 respectively. x_{4} further drives x_{5} and they both share a feedback loop. Similarly, in Dataset 2, x_{1} drives x_{2} with time lag 3 and x_{2} in turn drives x_{3}. x_{1} and x_{3} both together drive x_{4}. Similarly, in Dataset 3, we have x_{1} driving x_{2}. x_{2} drives x_{3} with lag 2 and x_{3} in turn drives x_{4}. The process x_{5} is driven by x_{2} and x_{4} with time lag 2 and 1 respectively. In the end, x_{6} receives the drives from x_{1}, x_{5} and x_{3} with time lags 2,1 and 3 respectively.
The datasets are disjoint from each other due to different sources of initiation. The datasets show different arrangements of connections between the processes which include feedback loops, low and high coefficients of drive between processes, multiple processes together driving a single process and all the processes interacting with other processes on a different time lag.
We see in Figure 1 for (Dataset 1) that node 1 connects to nodes 2,3 and 4. Nodes 4 and 5 are also connected in the inferred network structure. The equations describing the Dataset 1 reflect these facts. One of the extra link present is the interaction of node 2 with node 3 showing the fact that nodes 2 and 3 are both driven by node 1. They exhibit an interaction according to the F-test criteria but their strength is very low compared to other interactions. Since node 1 is also a driving force for node 4, so according to the previous argument, nodes 2 and 3 are also found to drive node 4. Node 4 and node 5 share a feedback loop, thus an interaction between them exists. There is a similar situation with nodes 1,2 and 3 interacting with node 5 due to node 1 being the common driving force behind nodes 2 and 3.
The connections are simpler and more sparse in the case of Figure 2 for Dataset 2 where there is an extra edge not described by the system of equations is present in the inferred network. Similarly in the network obtained for Dataset 3, the influence of node 1 on nodes 3 and 5 can be attributed to the fact that the influence is propagating through node 2 which is directly regulating nodes 3 and 5. The influence of node 2 on 6 is due to node 2 being the driving force for node 3 which in turn is directly influencing node 6. In the similar fashion, the dashed line between nodes 4 and 6 can be explained due to node 4 driving node 5 which in turn is driving node 6.
Experiments with Real Datasets: Material
We test our method on real biological dataset obtained from in-house microarray experiment designed to measure gene-expression level of around 31,000 genes for Arabidopsis thaliana plant [44]. This section summarizes the experimental details at different stages to obtain the data.
Plant growth and leaf material acquisition
Arabidopsis (COL-0) was grown in a controlled environment at 20°C, 70% relative humidity, 250 μ mol m-2s-1 light intensity, 16 h day length. Leaf 7 was tagged on emergence and biological replicates were harvested both the morning and evening (7 h and 14 h into light period) at 2 day intervals until fully senescent. This resulted in 22 time point samples from before full expansion to senescent.
RNA isolation and probe preparation
RNA was isolated from 4 individual leaves as separate biological replicates using the Triazol method (Invitrogen) followed by RNeasy column purification (Qiagen). RNA was amplified using a MessageAmp II (Ambion) and then labeled with Cy3 or Cy5 using reverse transcriptase (SuperScript II, Invitrogen). Each amplified RNA sample was labeled twice with Cy3 and twice with Cy5 giving 4 technical replicates for each leaf sample. Two Cy3 and C5 labelled samples (in 25% formamide, 5× SSC, 0.1% SDS and 0.5 mg ml-1 yeast tRNA) were mixed in different combinations for hybridization to microarray slides.
Microarray analysis
Microarrays (CATMA) carrying 31,000 Arabidopsis gene probes (constructed in house as described in [44]) were hybridized with labeled samples at 42°C overnight. Slides were washed and then scanned using an Affymetrix 428 array scanner at 532 nm (Cy3) and 635 nm (Cy5). Scanned data were quantified using Imagene version 7 software (BioDiscovery, http://www.biodiscovery.com/).
Individual text files quantifying the output for Cy3 and Cy5 were used in the further data analysis.
Experiments with Real Datasets: Small Example
After testing our method on the synthesized datasets, we test our method on the Arabidopsis data discussed above. We test our method on two samples of different sizes of the same dataset. We first test our method on a smaller sample of 85 genes belonging to three different categories of biological processes. This smaller sample helps us mimic the scenario shown by our synthetic model. The primary advantages of choosing the smaller dataset is that it helps us in minimizing the search space for ontological validation of clusters by mining on-line repositories which may not be complete for all the genes. Later, we apply our technique on a larger dataset of 1800 genes and study the clusters obtained and the general structural properties of the network.
The vertices with higher degree are bigger in size. The size of a vertex is decided according to the total degree associated with it. The biological relevance of the degree distribution of nodes in a biological network is discussed later in the paper.
Gene ontology details for the networks shown in Figure 7
GO-ID | p-value | corr p-value | Known/Total | Functional Description | Gene Names |
---|---|---|---|---|---|
Figure 7(A) | |||||
48511 | 1.3744E-11 | 4.1921E-10 | 4/6 | Rhythmic process | AT5G02810, AT2G46830, AT1G68830, AT2G25930 |
7623 | 1.3744E-11 | 4.1921E-10 | 4/6 | Circadian rhythm | AT5G02810, AT2G46830, AT1G68830, AT2G25930 |
Figure 7(B) | |||||
9814 | 4.5406E-11 | 7.6281E-9 | 5/8 | Defense response | AT1G55490, AT2G34690, AT5G03280, AT1G61560, AT4G14400 |
45087 | 2.5439E-10 | 2.1369E-8 | 5/8 | Innate immune response | AT1G55490, AT2G34690, AT5G03280, AT1G61560, AT4G14400 |
6955 | 3.8828E-10 | 2.1743E-8 | 5/8 | Immune response | AT1G55490, AT2G34690, AT5G03280, AT1G61560, AT4G14400 |
2376 | 5.7329E-10 | 2.4078E-8 | 5/8 | Immune system process | AT1G55490, AT2G34690, AT5G03280, AT1G61560, AT4G14400 |
8219 | 3.9627E-9 | 1.1096E-7 | 4/8 | Cell death | AT1G55490, AT2G34690, AT5G03280, AT4G14400 |
16265 | 3.9627E-9 | 1.1096E-7 | 4/8 | Death | AT1G55490, AT2G34690, AT5G03280, AT4G14400 |
Figure 7(C) | |||||
7623 | 1.6563E-14 | 9.8551E-13 | 5/7 | Circadian rhythm | AT5G57360, AT2G46790, AT1G22770, AT5G61380, AT4G08920 |
48511 | 1.6563E-14 | 9.8551E-13 | 5/7 | Rhythmic process | AT5G57360, AT2G46790, AT1G22770, AT5G61380, AT4G08920 |
Figure 7(D) | |||||
16280 | 3.0760E-13 | 1.4149E-11 | 5/6 | Aging | AT3G12090, AT4G23410, AT5G14930, AT2G19580, AT2G21045 |
32502 | 1.1218E-8 | 2.5802E-7 | 6/6 | Developmental process | AT3G12090, AT4G23410, AT3G44880, AT5G14930, AT2G19580, AT2G21045 |
The subgraph in Figure 7(a) is composed of 8 genes (AT5G02810, AT1G68830, AT1G63260, AT2G46830, AT5G65970, AT5G15850, AT1G67070, AT2G25930). 6 out of the 8 genes are known in the GO database. No annotations could be obtained for the remaining 2 genes (AT5G65970 and AT1G67070). 4 out of the 6 known genes are clearly known as the genes participating in the circadian rhythm process. AT5G15850 is known to be associated with the regulation of flower development which is related to the circadian rhythm of the Arabidopsis plant. Gene AT1G63260 is wrongly classified as it is known to participate in the aging process. Similarly, in the second network (Figure 7(b)), there are 13 genes in all(AT1G09530, AT4G14400, AT2G19450, AT2G02990, AT5G51810, AT5G20250, AT3G16770, AT2G29350, AT3G45290, AT1G55490, AT1G61560, AT2G34690, AT5G03280). 8 of the genes have entries in GO and no annotation could be found for the remaining 5 genes (AT1G09530, AT5G51810, AT5G20250, AT3G45290 and AT3G16770). 5 out of the 8 known genes are involved with the biological process of defense, immune response and cell death. AT2G19450 and AT2G02990 are known for 'response to stress'(GO process ID - 9651). Gene AT2G29350 is classified for 'aging' and is the odd member in the network. The third network shown in Figure 7(c) has 10 genes (AT2G44110, AT5G61380, AT4G08920, AT5G57360, AT2G46790, AT5G60100, AT1G79230, AT3G46640, AT5G57810, AT1G22770) with 7 of them known in the GO database and 3 (AT3G46640, AT1G79230, AT2G44110) are without any annotation. 5 out of the 7 annotated genes are known to participate in rhythmic activity. Gene AT5G60100 is known for regulation of circadian rhythm (GO process ID - 42752). Gene AT5G57810 is known for 'aging' and is wrongly put in this network. The last subnetwork shown in Figure 7(d) is composed of 8 genes (AT4G23410, AT5G14930, AT3G44880, AT4G30270, AT2G17480, AT2G21045, AT2G19580, AT3G12090). 6 out of the 8 genes are known in the GO database. All the 6 genes are known to participate in aging process of the plant. No annotations were found for genes AT2G17480 and AT4G30270.
Experiments with Real Datasets: Bigger Example
GO annotations for the highlighted genes shown in Figures 8-14
GO-ID | p-value | corr p-value | Known/Total | Functional Description | Gene Names |
---|---|---|---|---|---|
Figure 8 | |||||
6950 | 5.1715E-13 | 5.6542E-11 | 18/38 | Response to stress | AT3G08730, AT5G27600, AT4G33030, AT1G53670, AT2G37220, AT4G34710, AT4G31550, AT5G54810, AT4G09650, AT4G29040, AT5G24770, AT2G14610, AT3G51780, AT3G53990, AT4G04020, AT1G16880, AT5G25610, AT5G02500 |
Figure 9 | |||||
44444 | 3.5066E-4 | 2.0147E-2 | 7/11 | Cytoplasmic part | AT5G42020, AT3G62030, AT1G27450, AT4G37910, AT2G45030, AT5G50950, AT1G69370 |
Figure 10 | |||||
51869 | 5.5701E-12 | 2.3450E-9 | 20/41 | Response to stimulus | AT5G20850, AT5G55120, AT3G08720, AT4G37680, AT5G26870, AT1G33560, AT2G47180, AT2G05520, AT1G48030, AT4G01060, AT5G37780, AT1G63840, AT2G14580, AT1G58220, AT3G26790, AT3G54320, AT5G10450, AT1G74310, AT5G45340, AT5G40350 |
Figure 11 | |||||
9628 | 1.1048E-5 | 1.3147E-3 | 4/7 | Response to abiotic stimulus | AT5G52310, AT3G17020, AT5G67030, AT5G63890 |
Figure 12 | |||||
3824 | 9.0400E-4 | 4.2857E-2 | 10/15 | Catalytic activity | AT2G17420, AT3G15020, AT5G04590, AT3G13235, AT1G23190, AT3G53160, AT3G48090, AT4G23600, AT4G08790, AT1G51680 |
Figure 13 | |||||
6950 | 7.0271E-10 | 6.6055E-8 | 14/37 | Response to stress | AT5G20230, AT5G61900, AT4G16845, AT3G22370, AT2G04030, AT1G55490, AT3G11820, AT4G12400, AT4G34990, AT4G23100, AT4G20260, AT3G49910, AT5G09810, AT5G05410 |
Figure 14 | |||||
44464 | 2.6470E-3 | 1.8771E-2 | 25/36 | Cell part | AT4G27670, AT5G59220, AT4G25100, AT3G58810, AT4G14630, AT3G53620, AT5G11520, AT3G27300, AT1G42970, AT5G43280, AT4G27430, AT1G49300, AT2G39460, AT2G37040, AT3G01480, AT5G24550, AT1G72140, AT5G62790, AT1G25540, AT1G02860, AT4G38970, AT2G43130, AT3G52960, AT3G01220, AT2G43750 |
Simple network statistics
We computed certain network statistics to confirm that our network is not a randomly generated network and has the properties desired in a biological network. A total of 1353 nodes were present in the network after filtering out weaker edges. The total number of edges present in the network was 21,214 which is around 1.1% of the total possible directed edges in the network, which is an indication of sparseness, a common characteristics of biological networks [49]. There is one connected component in the network indicating strong connectivity. The mean shortest path length is 2.6 which means that most genes are close to each other and the network diameter representing the maximum distance between two connected nodes is 6. Both the phenomenon have been described as small world properties of real networks [50]. We also compute and report the following widely used topological properties for our network.
Node degree distribution
Shared neighbor distribution
Figure 15(b) shows the shared neighbor distribution for the network. P(i, j) is the number of partners shared between nodes i and j, that is, nodes that are neighbors of both i and j. The shared neighbors distribution gives the number of node pairs (i, j) with P(i, j) = k for k = 1,2, 3.... The distribution again shows a power law like distribution indicating the presence of motifs with large numbers of connected components in the network.
Closeness centrality
Closeness centrality is a measure of how fast information flows from a given node to other reachable nodes in the network. Closeness centrality (C) of a network with n nodes is computed as the reciprocal of the average shortest path length is computed as follows: C(n) = where L(i, j) is the length of the shortest path between two nodes i and j. Figure 15(c) plots the closeness centrality of all the nodes against number of neighbors. The isolated nodes have their closeness centrality equal to 0. An increasing trend of closeness centrality in our network further indicates strong connectivity and ability to form hubs.
Topological coefficient
Another characteristics of interaction networks can be captured by calculating the topological coefficients [51, 52]. The topological coefficient, TC(k), is a relative measure for the extent to which a gene in the network shares interaction partners with other genes. Also the topological coefficient as shown in Figure 15(d) decreases with the number of links (close to ), demonstrating that, relatively, in our network, hubs do not have more common neighbors than genes with fewer links. This indicates that genes with many links are not artificially clustered together. Moreover, it confirms the presence of modular structures in the network organization.
Comparison With Respect to Other Existing Methods
The correlation matrix for synthetic datasets 1, 2 and 3.
Dataset 1 | ||||||
---|---|---|---|---|---|---|
Node | 1 | 2 | 3 | 4 | 5 | |
1 | 1.0000 | 0.2613 | -0.2309 | -0.2500 | 0.0871 | |
2 | 0.2613 | 1.0000 | -0.7114 | -0.7515 | 0.1351 | |
3 | -0.2309 | -0.7114 | 1.0000 | 0.7654 | -0.1283 | |
4 | -0.2500 | -0.7515 | 0.7654 | 1.0000 | -0.3125 | |
5 | 0.0871 | 0.1351 | -0.1283 | -0.3125 | 1.0000 | |
Dataset 2 | ||||||
Node | 1 | 2 | 3 | 4 | ||
1 | 1.0000 | -0.0944 | 0.0621 | -0.1088 | ||
2 | -0.0944 | 1.0000 | -0.0940 | 0.6040 | ||
3 | 0.0621 | -0.0940 | 1.0000 | 0.0024 | ||
4 | -0.1088 | 0.6040 | 0.0024 | 1.0000 | ||
Dataset 3 | ||||||
Node | 1 | 2 | 3 | 4 | 5 | 6 |
1 | 1.0000 | 0.1872 | 0.0449 | 0.0329 | 0.1118 | 0.1531 |
2 | 0.1872 | 1.0000 | 0.1105 | 0.0292 | 0.0748 | 0.3101 |
3 | 0.0449 | 0.1105 | 1.0000 | -0.0001 | 0.2516 | 0.0665 |
4 | 0.0329 | 0.0292 | -0.0001 | 1.0000 | 0.0821 | 0.2282 |
5 | 0.1118 | 0.0748 | 0.2516 | 0.0821 | 1.0000 | 0.0907 |
6 | 0.1531 | 0.3101 | 0.0665 | 0.2282 | 0.0907 | 1.0000 |
The Euclidean distance matrix for synthetic datasets 1, 2 and 3.
Dataset 1 | ||||||
---|---|---|---|---|---|---|
Node | 1 | 2 | 3 | 4 | 5 | |
1 | 0 | 50.6180 | 60.5454 | 66.3305 | 53.7858 | |
2 | 50.6180 | 0 | 49.0080 | 57.3540 | 35.0406 | |
3 | 60.5454 | 49.0080 | 0 | 21.1572 | 36.9004 | |
4 | 66.3305 | 57.3540 | 21.1572 | 0 | 46.7355 | |
5 | 53.7858 | 35.0406 | 36.9004 | 46.7355 | 0 | |
Dataset 2 | ||||||
Node | 1 | 2 | 3 | 4 | ||
1 | 0 | 57.2707 | 49.4072 | 54.0319 | ||
2 | 57.2707 | 0 | 35.4161 | 23.3695 | ||
3 | 49.4072 | 35.4161 | 0 | 28.6682 | ||
4 | 54.0319 | 23.3695 | 28.6682 | 0 | ||
Dataset 3 | ||||||
Node | 1 | 2 | 3 | 4 | 5 | 6 |
1 | 0 | 32.1456 | 32.0493 | 31.7813 | 33.2172 | 34.6842 |
2 | 32.1456 | 0 | 25.0916 | 25.6146 | 28.3732 | 27.0407 |
3 | 32.0493 | 25.0916 | 0 | 21.9953 | 22.6557 | 28.4800 |
4 | 31.7813 | 25.6146 | 21.9953 | 0 | 24.4613 | 25.7756 |
5 | 33.2172 | 28.3732 | 22.6557 | 24.4613 | 0 | 30.6190 |
6 | 34.6842 | 27.0407 | 28.4800 | 25.7756 | 30.6190 | 0 |
In an ideal scenario, where the genes performing similar activity group together, we expect three distinct regions in Figures 16 and 17. The lower diagonal blocks from cell 1 to 30, cell 31 to 64, and cell 65 to 85 should indicate a high degree of intra-block association, each block should be colored in different shades of red according to the color-magnitude mapping shown in the color-bars. But, this is not the case in the figures obtained by us where we can see no clear blocks in the figures. The lack of any block-wise patterns in the color coded cells of association matrices indicate the absence of strong associative information between genes based on the measures discussed above. This is the first indication that the measures like correlation and euclidean distance may not be suitable for our dataset.
GO annotations for clusters found in the smaller Arabidopsis dataset using correlation as the measure of association between genes
GO-ID | p-value | corr p-value | Known/Total | Functional Description | Gene Names |
---|---|---|---|---|---|
Figure 18(A) | |||||
48511 | 4.0370E-9 | 8.2759E-8 | 3/4 | Rhythmic process | AT5G24470, AT2G46790, AT5G61380 |
Figure 18(B) | |||||
16280 | 2.8611E-12 | 2.0600E-10 | 5/8 | Aging | AT5G45900, AT2G29350, AT5G35630, AT3G10985, AT4G28050 |
We have used a fresh and distinct approach to cluster temporal microarray gene expression data. One of the key questions that we have tried to address using this method is that how some variables are useful for forecasting others. The proposed method facilitates a way to study such forecasting relationships between two variables. In other words, we are asking if a variable X can predict another variable Y. Equivalently, we can say if X is exogenous in time-series sense with respect to Y or not. Yet a third expression meaning the same thing is, if X is linearly informative about future Y. The basic idea behind this method is, if an event X causes another event Y, then X should precede Y in time. This is why our illustrative models are based on time, and within that time frame the lags like t - 1, t - 2, ⋯ etc. denote the temporal association within the processes.
While discussing widely used pairwise association methods for clustering, like any form of correlation or distance based methods, the time is static. In these methods, the time does not play any role. The core of these methods rely on association rather than prediction. So if we re-order the sequence of observations for any pair of variables (X, Y), the association measure between them does not change. As for example, let the original observation be X = {x_{t-1}, x_{t-2}, x_{t-3}} and Y = {y_{t-1}, y_{t-2}, y_{t-3}}. The Association measure using correlation/distance for (X, Y) = C. After reordering of the observations, let X' = {x_{t-3}, x_{t-1}, x_{t-2}} and Y' = {y_{t-3}, y_{t-1}, y_{t-2}}. The new association measure using correlation/distance for (X', Y') = C' where C = C'. Hence, this assumption is not suitable for dynamical systems. This is the reason why the usual pairwise association methods can give us less reliable results than the ones by our method. And hence a comparison between the two methods will not be fair. There has been some work in model based clustering methods based on Bayesian statistics where the dynamics of profiles (modeled as regressive processes) have been used to create clusters [39, 53]. Such methods are different from our approach as, first, our approach is based on the frequentist approach rather than the Bayesian approach, and second, the essence of our approach lies in detecting the causal association between genes. Another important aspect to consider is the choice of time lag in our method which is decided using the AIC criteria. The lag value is not fixed, but is chosen iteratively for each individual pair (X, Y) according to what describes the variables best.
We have demonstrated the performance of the method using various artificial datasets and examples from real biological datasets. It is easy to see that the pair-wise association based techniques, like distance or correlation based measures, would not work as desired, when we are investigating a system where the interaction with respect to time is an important concept.
Conclusions
Clustering helps in reducing the data dimensions by grouping genes with similar profiles or similar functionalities. In this paper, we proposed a clustering method to group functionally related genes in a temporal microarray dataset. Our method exploits the temporal interdependence between genes. The interdependence was determined using the test of Granger causality between two time series. The method is simple in its implementation, and testable at every stage. We analyze the association graph using a graph-theoretic method to detect the dense regions in the graph. These dense regions could be indicators of potential biological complexes and motifs. The graph-theoretic approach helps us in detecting the functionally interesting regions in a large network derived by the Granger causality test. We test our approach using a set of artificial datasets and two datasets of different sizes belonging to the Arabidopsis experiment. The functional similarity between genes belonging to detected clusters was verified using the publicly available gene ontology database. We further analyzed the structural properties of the association network obtained for the larger of the two datasets for Arabidopsis. We show using different network characteristics that the computed association network is not a random network in its structure, and has the properties expected in a real biological network.
There are few considerations which should be taken into account while applying this approach. The data must be cleaned properly using appropriate normalization method to remove unwanted experimental biases. For any time-series based statistical method, it is important that the data has been collected at intervals which capture the natural changes in the system. Selection of correct lag order using an information based criteria is also important as the test of Granger causality is strongly dependent on that decision. Due to the small number of time points in our dataset, we have used linear form of Granger causality to establish relationship between genes in our model. It should be noted that Granger causality test is not restricted to only linear models, and it can be readily extended to include non-linear terms in case we observe any non-linear behavior in the data. Some examples of non-linear extension if Granger causality can be found in the publication by Ancona et al. [54] and Marinazzo et al. [55]. Most important of all, the experimental design should be able to support the hypothesis of the practitioner. Further care should be taken while discovering directional causal links using Granger causality [9, 10]. It should be noted that multivariate approaches instead of pair-wise to detect interactions between genes can give better result while re-engineering a causal network structure from data [11, 48, 56, 57]. In this paper, our effort was not to detect a causal network structure from gene data, but to find a suitable association matrix based on interactions between them. Once the interesting modules have been found, different reverse engineering methods like Bayesian networks, Structural equations etc. can be applied to infer causal networks from selected genes of interest.
Methods
Inference of Causal Association
- 1.
- 2.
- 3.
Feedback: The feedback between X and Y exists if X is causal to Y and Y is causal to X.
Feedback is only defined for the case of simple causal relations because the direction of instantaneous causality cannot be determined without additional information or assumption.
where ϵ_{ t }is the prediction error or residual.
If the test statistic S is greater than the specified critical value specified critical value, we reject the null hypothesis that Y does not Granger-cause X.
where σ is the estimated noise covariance, m is the dimension of the stochastic process and n is the length of the data window used to estimate the model.
We will use the test of Granger causality to establish association between gene pairs in our interaction network. If the test for causality passes in any direction, either from X → Y or from Y → X, we add an edge in the network. We are not interested in the direction of the edge and the association network is not directional at all.
Detection of Dense Regions in Association Graph
Even though most of the biological networks are sparse in their connectivity, the complexity of connections increases with the increasing number of nodes. A network of interacting entities can be readily modeled as a graph where the entities are represented by nodes and the associations between them as edges. It is often argued [61, 62] that graph theoretic approaches can help analyze large interacting networks to find clusters (highly dense regions) in a network. Clusters in a gene-gene interaction network are often biological complexes or part of biochemical pathways [63]. Algorithms for finding clusters or highly dense regions are an ongoing topic of research and are often based on network flow theory [64] or spectral clustering [29]. We use a clustering method proposed by Bader and Hogue [65] to detect the dense regions in the association network obtained by our Granger causality based method. The method weighs all the vertices based on their local network density to detect dense regions in the graph. The decision to use this algorithm to analyze our association matrix was based on two reasons: a) this is one of the earliest methods to use a clustering algorithm to identify molecular complexes in a biological network, and hence is widely known, and, b) it has a publicly available software plug-in for a widely used network analysis platform called Cytoscape [61]. Thus, the method and its implementation are both widely used and tested. It should be noted that application of other clustering methods to detect dense regions can produce different clusters and some may have better performances but these are not tested here.
The functioning of the method by Bader and Hogue can be understood in the following way. Given a graph G = (V, E), where V and E being the sets of vertices and edges respectively, the density of a graph is based on the connectivity level and is defined as D_{ G }= |E|/|E_{ max }|, where E_{ max }is the total number of all possible edges in a complete graph G.
The vertex weighting in the graph starts by weighing all the vertices based on their local network density using the highest k-core of the vertex neighborhood. A k-core is a graph of minimal degree, ∀v ∈ V and the degree of v ≥ k. The highest k-core of a graph is the central and most densely connected subgraph. The highest k-core component gives us the highest k-core level, k_{ max }in the vertex neighborhood. The final weight of the vertex is the product of k_{ max }and the density of the corresponding highest k-core component.
This type of weighting amplifies the weighting of heavily connected graph regions while removing the less connected graph regions which are present in abundance.
Once the vertex weighting is done, the algorithm seeds a subgraph(complex) with highest weighted vertex and moves outwards to include vertices in the neighborhood whose weight is greater than a given threshold. The algorithm propagates through the included neighbors and recursively checks the subsequent nodes. The process stops when no more nodes can be added to the complex and is repeated for the next highest unseen weighted vertex in the network.
In the post-processing stage, the complexes which do not contain at least 2-core (graph with minimum degree 2) are filtered out. Finally, all the complexes in the network are scored and ranked. The complex score for a given subgraph G_{ C }= (V_{ c }, E_{ c }) is defined as the product of the density of the subgraph and the number of vertices (D_{ c }× |V_{ c }|). Other scoring schemes are also possible but are not tested in the original algorithm.
Declarations
Authors’ Affiliations
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