Skip to main content

Advertisement

We’d like to understand how you use our websites in order to improve them. Register your interest.
Download PDF

eXamine: Exploring annotated modules in networks

BMC Bioinformatics volume 15, Article number: 201 (2014) Cite this article

Abstract

Background

Biological networks have a growing importance for the interpretation of high-throughput “omics” data. Integrative network analysis makes use of statistical and combinatorial methods to extract smaller subnetwork modules, and performs enrichment analysis to annotate the modules with ontology terms or other available knowledge. This process results in an annotated module, which retains the original network structure and includes enrichment information as a set system. A major bottleneck is a lack of tools that allow exploring both network structure of extracted modules and its annotations.

Results

This paper presents a visual analysis approach that targets small modules with many set-based annotations, and which displays the annotations as contours on top of a node-link diagram. We introduce an extension of self-organizing maps to lay out nodes, links, and contours in a unified way. An implementation of this approach is freely available as the Cytoscape app eXamine

Conclusions

eXamine accurately conveys small and annotated modules consisting of several dozens of proteins and annotations. We demonstrate that eXamine facilitates the interpretation of integrative network analysis results in a guided case study. This study has resulted in a novel biological insight regarding the virally-encoded G-protein coupled receptor US28.

Background

High-throughput “omics” data provide snapshots of cellular states in a specific condition. Computational approaches can be used to relate these low-level measurements with high-level changes in phenotype. Traditionally, these approaches were gene-centric and typically resulted in ranked lists of differentially expressed genes [1–3]. Later, gene-centric approaches were complemented by pathway- [4, 5] and network-based methods [6, 7] to provide inter-gene context for mechanistic insights. Pathway-based approaches identify overrepresented pathways from databases such as the Kyoto Encyclopedia of Genes and Genomes (KEGG) [8]. Network-based approaches yield small, de novo subnetwork modules that may span several known pathways, and reveal their crosstalk [9].

Extracted network modules are analyzed in the context of established gene annotations to hypothesize about the module’s role in high-level cell conditions (see Figure 1). Genes are often related to very many terms (too many for human comprehension), most of which are likely irrelevant to the analysis context. Therefore, overrepresentation analysis is performed to rank information items by their significance. These items originate from ontologies such as the Gene Ontology (GO) [10], which identifies cellular functions, processes and components that nodes relate to, or from KEGG [8], which relates nodes to pathways. This results in an annotated module, which retains the original network structure and includes enrichment information as a set system.Existing tools focus on visualizing large networks, and have only limited or separate set system support or no support at all. Our proposed visual analysis approach displays sets as contours on top of a node-link layout (see Figure 2). It treats module edges and annotation sets in a unified way, and contributes the following to the analysis of annotated modules:

Figure 1
figure1

Data and analysis pipeline. First, control and experimental samples are analyzed to estimate expression levels. Subsequently, gene expression differences (between experiment and control) and their significance are determined. These differences are then mapped to an interaction network, from which a module is extracted with overall significantly-differential gene expression. This module is annotated with overrepresented cell mechanisms from ontology and pathway databases. Finally, the enriched module undergoes iterative visual analysis via eXamine.

Full size image
Figure 2
figure2

Visualization of an annotated module. Interacting proteins with a selection of three subsets, corresponding to overrepresented KEGG pathways. The visualization consists of a combination of a node-link diagram and an Euler diagram.

Full size image

  • Identification of elementary module analysis tasks and their composition into a visual analysis process;

  • Extension of the self-organizing maps (SOM) algorithm to lay out module interactions and annotations in a unified approach;

  • Implementation in the form of the Cytoscape app eXamine;

  • Demonstration of eXamine via a guided study of an annotated module that is activated by the virally-encoded G protein-coupled receptor US28;

  • Discussion on how eXamine facilitates the analysis process.

Data characteristics

The annotated modules—targeted by the presented method—have the following characteristics.

D1 Small and sparse network topology, in which genes and interactions number in the dozens;

D2 Many annotation sets, outnumbering gene interactions;

D3 Annotation sets vary in cardinality, from a single node to the entire module;

D4 Annotation sets overlap often.

Integrative network analysis methods produce small and sparse subnetwork modules (D1), rather than large lists of differentially expressed genes. Embedding the module in a rich context of annotations on overlapping sets of genes is a typical next step to gain insights in the underlying biology (D2, D3, D4).

Analysis tasks

The focus (or perspective) of analysts alternates between genes (and interactions within a module) and annotation sets. Important analysis tasks are supported for each of these data aspects to enable an analyst to hypothesize about the role of an extracted module in light of experimental conditions.

For genes, analysts want to determine:

G1 Level of differential expression: under- or over-expressed, or insignificant;

G2 Interacting neighbors;

G3 Annotations (set memberships);

G4 Annotations shared with other genes.

Single genes can become the focus of attention during the analysis process within the context of the module. The fact that a gene is part of a module does not imply that its under- or overexpression is significant. However, information (G1) about differential expression enables the elucidation of a gene’s presence in the module. For example, it could be the case that a gene is not differentially expressed significantly itself, but that it is still part of a module, because it connects two differentially expressed submodules. An indirect involvement of the gene in a module mechanism is therefore likely. Neighboring genes might also become interesting (G2), as are any mechanisms that it is associated with already (G3), and the mechanisms that it shares with other genes in the module (G4).

For annotation sets, analysts want to determine:

A1 Significance of overrepresentation;

A2 Gene memberships.

If a specific gene is interesting, its annotations might be too (G3 and G4). Annotation sets themselves can have such significance (A1) that they become interesting, which then translates to genes contained in them (A2). Both significance in terms of an associated p-value and subjective significance are of importance to divide attention between annotation sets.

For interactions, analysts want to determine:

L Annotation transitions between interacting genes.

A change between annotations (L) may occur when the focus on a gene shifts to a neighboring gene (G2), which is of importance to an analyst to judge the role and relevance of the neighboring gene in the module.

Related work

Network visualization and tools.

Many advanced techniques for the visualization of network topology have been developed [11–13], but few have been transferred to readily available tools. On the other hand, there are many tools for interpreting and exploring biological networks [14], including the popular open source platforms Cytoscape [15] and PathVisio [16]. However, these currently provide only limited capability to visualize annotated modules. PathVisio is a pathway analysis approach, in which sets are restricted to subsets of static, pre-defined individual pathways, and set membership is conveyed via node colors. Cytoscape’s group attributes layout can be used to visualize partitions by showing disjoint parts in separate circles, but it does not support overlapping sets. The Venn and Euler diagram app [17] for Cytoscape does support overlapping sets, but it can handle only four at the same time (see Figures 3(a) and (b)). In this app, network and sets are visualized separately: set membership is conveyed by selecting a set and its corresponding nodes are highlighted in Cytoscape’s network view. The RBVI collection of plugins [18] facilitates creation and editing of Cytoscape groups, and provides a group viewer that relies on aggregation of groups into meta-nodes. These meta-nodes can be visualized as standard nodes, as nodes containing embedded networks, or as charts. This approach, however, does not allow for visualization of overlapping sets.

Figure 3
figure3

Comparison. Annotated module visualization using Cytoscape’s Venn and Euler diagram app: (a) Venn diagram and (b) Euler diagram. The number of displayed sets is limited to four and no network structure is shown. (c) Module laid out by one of Cytoscape’s built-in force-directed layout algorithms and BubbleSets superimposed on the network (same color scheme as in Figure 8(b)). Note that it is not immediately apparent that the nodes in the β-catenin set (blue) form a subset of Adherens junction (yellow), because the BubbleSet approach applies no explicit nesting of subsets.

Full size image

Set system visualization

In the information visualization field, Euler diagrams are used for the intuitive visualization of set systems [19–21], in which items belonging to the same set are denoted by contours. Variants of these approaches visualize sets over items with predefined positions, e.g., over a given node-link visualization of a network. These methods range from connecting these items by simple lines (LineSets) [22], via colored shapes that are routed along the items (Kelp Diagrams) [23] and contours around the items (BubbleSets, see Figure three(c)) [24, 25] to hybrid approaches (KelpFusion) [26]. Visualizing an annotated module, however, requires an integrated layout of both its network and set system topologies, which is not possible with these approaches. Euler diagram methods focus on the layout of set relations at the expense of network topology. Likewise, laying out the network before superimposing set relations will emphasize network topology to the detriment of the set system. Some techniques exist that provide such integrated layouts [27–30], and which include aesthetic concerns and design of visual metaphors [31]. However, these approaches assume constraints on the network and set system topologies, e.g., strict partitions and no overlapping sets, and they are therefore not applicable to our problem.

Method and implementation

Visualizing an annotated module amounts to visualizing a hypergraph consisting of binary edges (interactions) between nodes (genes) and n-ary edges (annotation sets). Analysis tasks G2-G4 and A2 establish the equal importance of associating interactions and annotation sets, which reflect on both the layout as well as the visualization of the hypergraph. Therefore, as opposed to combining multiple existing techniques—e.g., a force simulation to position the nodes according to the binary edges [32], a node overlap removal algorithm to keep nodes identifiable [33], and subsequent construction of a density field to derive contours for annotation sets [24]—our approach relies on a unified algorithm that treats binary and n-ary edges on equal terms. This allows us to compute a balanced layout, and also to choose suitable representations for the binary and n-ary edges. Mathematically, we achieve this by assigning a bit vector t=(t1,t2,…,t M ) to every node t∈V (the module genes) that encodes its membership in binary and n-ary edges S1,S2,…,S M . That is, t i =1 if t∈S i and t i =0 if t∉S i .

To make this representation more concrete, consider the annotated module shown in Figure 2. The nodes are represented as the set V={Calm1, Calm2, Calm3, Kras, Nr3c2, Plcb4 }. There are seven sets representing the edges and three sets representing pathway memberships. The edge sets are S1={v1,v4}, S2={v1,v6}, S3={v2,v4}, S4={v2,v6}, S5={v3,v4}, S6={v3,v6}, and S7={v4,v5}. Note that nodes v4 (Kras) and v6 (Plcb4) have some additional outgoing edges, but their targets are not visible in the image. Therefore, we ignore these edges in this example. The pathway memberships are the Glioma set S8={v1,v2,v3,v4}, the Long-term potentiation set S9={v1,v2,v3,v4,v6}, and the GnRH signaling pathway set S10={v1,v2,v3,v4,v6}. Now, for example, node v5 gets assigned the bit vector t v 5 =(0,0,0,0,0,0,1,0,0,0) and node v6 the bit vector t v 6 =(0,1,0,1,0,1,0,0,1,1).

This high-dimensional representation is then used to lay out the nodes without overlap, the binary edges as curves, and the n-ary edges as contours.

Extension to self organizing maps

Self Organizing Maps (SOMs), introduced by Kohonen [34], are artificial neural networks that are used to map high-dimensional data items to discretized low dimension. SOMs are used in a visualization setting to cluster similar items together in a 2D embedding, which results in a landscape of items based on their features [35, 36]. Typical SOMs consist of a square grid of size N×N with a neuron nx,y∈[0..1]M at every grid cell. A neuron nx,y is a bit vector of size M whose dimension matches the data items’ dimensions. In our case, the data items correspond to the set of nodes V in the annotated module. The training algorithm applies unsupervised reinforcement learning in an iterative fashion: at every iteration i∈{1,…,I} all data items t∈T are considered and the neuron that matches t most closely is determined using a distance function such as the Euclidean or Manhattan norm. This neuron and its neighboring neurons within radius r i are updated to match t even more closely by setting their respective vectors q to q+α i (t−q)—see Figure 4(a). In early iterations i, the trained neighborhoods are large with r i close to the grid size N and the training strength α i close to 1. The parameters r i and α i decrease monotonically with increasing i. As such, items that differ strongly will distribute across the map to establish their own regions in the grid at early stages. Items with smaller differences are separated along the grid at a more local level as the training iterations progress.

Figure 4
figure4

Training neuron n x , y . (a) The neighborhood within range r i is trained (colored gray). (b) Certain tiles are already reserved (colored red) in the RSOM algorithm, item t therefore trickles outwards to the best matching free spots (outlined).

Full size image

Reservation-based training.

Similar items may end up at the same grid position in a standard SOM. This issue is usually solved by showing aggregate depictions of items, but we need to have separate depictions without overlap to support tasks G1-G4. Therefore, each item has to map to a unique grid position. We achieve this by altering the training algorithm:

The algorithm assigns items to a unique neuron after every training iteration, because, once a neuron is reserved by an item, subsequent items will ignore it. This causes a flooding effect where similar items end up in the same area of the grid and trickle outwards as the area becomes more crowded—see Figure 4(b).

Configuration.

The metric distance form of cosine similarity is used as the distance function d, i.e. d(q,p)= cos−1((q·p)(|q||p|))π−1. This measure outperforms the Euclidean and Manhattan norms in high-dimensional spaces. The SOM is trained with a learning strength and neighborhood range that decrease linearly with increasing iteration i. A standard choice is α i =c·(1−i/I) and r i =⌊(1−i/I)·N⌋, where c∈(0..1) is a small constant that determines the initial training strength. We use N=2|T| for the number of neurons and iterations, balancing node placement freedom versus required display space, and I=1 0 6 /|T| for a gradual and accurate training, respectively.

Layout preservation.

A new layout has to be computed whenever the user selects or deselects a set. The new layout should change little in comparison to the old layout to preserve the user’s mental map. This is achieved by a simple addition to the SOM algorithm, where a new SOM is initialized with the previous configuration of the neurons, i.e., an item that was positioned at nx,y in the old SOM is placed at nx,y in the new SOM and its neighborhood is trained according to the new bit vector of the item. The new SOM retains much of the initial configuration by starting the training factor α i at c=0.01. Naturally, this imposes a trade-off between layout quality and conservation. The layout will sometimes change strongly to accommodate the addition of a set that contains many items. In contrast, the layout can be retained if only a small set that does not alter much of the topology is added. This approach does not consider a history of topological changes, as is done in online graph drawing [37] to capture temporal dynamics, but is sufficient to maintain a stable and interactive environment.

Set dominance.

The user is enabled to make a certain set more dominant in the layout by having the training algorithm place the items of that set closer to each other than the items of other sets. This relies on weighting the components of the item bit vectors: every S i is given a weight w i with w i =1 initially. The bit vectors are augmented to incorporate these weights: t i =w i if t∈S i and t i =0 if t∉S i . The bit vector component of S i will therefore play a more prominent role in distance metric d when the user increases w i —see Figure 5.

Figure 5
figure5

Changing the dominance of a set. (a) Highly dominant set, drawing proteins of the set together. (b) Non-dominant set, where the network topology fully defines the layout.

Full size image

Assigning greater weight to a set improves the quality of its layout by coalescing its elements, which aids tasks G4 and A2. However, it also degrades the layout quality of other sets and links when their topology conflicts with the prioritized set. This stems from the difficulty of projecting elements from a high-dimensional space down to a two-dimensional space, which sometimes results in a sub-optimal layout per set. Interactive manipulation provides a way to assign different priorities to sets, and improve their layouts.

Contours.

The SOM’s neuron grid is used to define the contours representing the active set system. Let S i be an active set. The corresponding i-th components of the neurons define a scalar field that forms a fuzzy membership landscape for S i . This field is similar to the density field used in Bubble Sets [24]. Now, the inclusion of the grid tile of neuron n in the contour body is determined by imposing a threshold, of for example 1 2 , on the i-th component (see Figure 6(a)). The contour can then be tightened to reduce sharp corners by including parts of tiles that are free of items, as illustrated in Figure 6(b).

Figure 6
figure6

Derivation of contours for set S i . The darkness of a tile represents the value of the neurons’ i-th component, the thick black line is the contour, dots represent items that are in S i , and white dots are items that are not in S i . (a) Contour that results from the union of tiles with a value above a certain threshold. (b) Refined contour with shortcuts across free tiles.

Full size image

After establishing the layout of the contours, we apply geometric post processing steps [23] to improve aesthetics, where all sets are legible (tasks G3 and A2) and contours form clear boundaries underneath interactions (task L). Sharp corners of the initial contours are rounded by a dilation of r, erosion of 2r, and subsequent dilation of r (see Figure 6). Here dilate and erode are equivalent to Minkowski sum and Minkowski subtraction operators with a circle of radius r[38], respectively. In addition, the contours are nested by applying different levels of erosion, enforcing a certain distance between them. The thick colored ribbons in Figure 7 are obtained by taking the body b of a contour, eroding it to get a smaller body b e , and taking the symmetric difference b−b e of b and b e to effectively cut b e out of b. Here, the extent of the erosions and dilations (radius r) is bounded by a fraction of the grid’s tile size. This guarantees that items are contained by a contour of S i if, and only if, these items are contained by S i .Set contours are drawn in descending nesting order, which is defined by their different erosion levels; the largest contour is drawn first and the smallest contour last. The contour ribbons are assigned unique colors per set and are drawn fully opaque to prevent any confusion caused by blended colors. Occlusion is mitigated by limiting the width of the ribbons. Finally, the contours are drawn a second time as dashed lines such that occluded contour sections can be inferred—see Figure 7.

Figure 7
figure7

Geometric refinement of set contours after initial layout. Corners are smoothened by dilation and erosion operations, and contours are given a thick and colored internal ribbon. Unique erosion levels create distance between contour outlines, and contour overlap is emphasized by dashed lines.

Full size image

Implementation

We have implemented the technique in a Cytoscape app, and have emphasized simplicity of interaction and visual presentation in the design. The available sets are sorted by significance and listed in the set overview on the left, where the significance of a set is visualized as a circle, scaled logarithmically and accompanied by its scientific exponent as text (task A1). The user may select sets for inclusion in the annotated network visualization to the right—see Figure 8(c). All described functionalities can be used at interactive speeds for networks up to dozens of nodes, edges, and active sets, including laying out the network with the RSOM training algorithm. Geometric operations on the contours, such as dilations and erosions, are performed via Java Topology Suite [39].

Figure 8
figure8

Item highlighting. (a) Hovered protein (Met) with emphasized interaction links to its neighbors on the right and emphasized sets (KEGG pathways) that contain this protein on the left. Sets outside of the list scope are grouped as markers at the top and bottom, where one set in the bottom group is emphasized. (b) Hovered set (Pathways in cancer) with emphasized member proteins, interactions, and contour.

Full size image

Interaction.

Interactions consist of simple mouse actions (see the video in the Supplemental Material). The inclusion of a set in the network visualization is toggled via the set’s label in the set overview or its contour in the network visualization (task A2). Additional information about a set or node may be obtained via a hyperlink to a web page provided in the input data, enabling quick access to external information sources such as the KEGG website. This approach keeps the tool flexible, i.e., the tool itself does not have to be altered every time a new kind of set or node from a different database is loaded.The links of a node are emphasized when it is hovered over (see Figure 9(a)) such that its direct neighborhood can be discerned from its surroundings (task G2). Moreover, sets that contain the hovered node are highlighted as well. Likewise, links can be hovered to highlight their nodes and common sets. Vice versa, the contours of a set are emphasized and its comprising nodes are highlighted when it is hovered over (see Figure 9(b)). This provides immediate feedback to the user about node-set relations (tasks G3 and A2) without having to select a set and consequently changing the layout of the network visualization.

Figure 9
figure9

Case study snapshots. Gene differential expression is shown as a colored box drawn around the node label (green for under-expression and red for over-expression). (a) The annotated module after tagging of the two familiar pathways Pathways in cancer and Phosphatidylinositol signaling system in C1 Two familiar pathways. (b) The annotated module after tagging functions Beta-catenin binding and Growth factor activity in C3 A twist of β -catenin and C4 Growing knowledge. (c) The fully annotated module, including annotation set overview, from which the hypothesis of C5 New insights is derived.

Full size image

The lists of annotations sets can be expanded and collapsed by clicking on their headers, and scrolled downward to sets of lower significance by turning the mouse wheel. The set circles that convey significance remain visible at all times, grouping at the list top and bottom, to guarantee the depiction of all set memberships when a node is hovered.The user can adjust the dominance of a set by spinning the mouse wheel while hovering over either the set’s label in the set overview or contour in the network visualization. This enables the user to give a set a central role in the layout (see Figure 5(a)) or to remove any of its influence (see Figure 5(b)).

All changes to the visualization caused by interaction are animated. Colors and positions of items are altered gradually. Link layout changes are animated by interpolating their control points, while contour layouts are handled by fading out the old contour and fading in the new contour. The use of layout preservation, as described previously, in combination with animations helps to preserve the user’s mental map.

Color.

Unique, distinguishable colors are derived from Color Brewer palettes [40], and assigned to annotation sets in a cyclic manner to avoid assigning the same color consecutively. In addition, large differences in contrast are avoided. For example, text and set outlines are colored dark gray instead of black to reduce their visual dominance. Black is only used when items are hovered over or highlighted such that they attract attention, as shown in Figure 9. Moreover, labels of selected sets (in the set overview) are emphasized with a more intense black color to ensure that they are readable in a colored surrounding. Node labels have a white background to make sure that their text is legible when drawn on top of a set ribbon with a dark color. Likewise, links have halos that make them easier to distinguish and their intersections more pronounced.

Cytoscape integration.

eXamine is tightly integrated into Cytoscape. Cytoscape’s group functionality is used to represent sets and we rely on the table import functionality for importing both the set and node annotations. The user is also able to group sets into different categories. The Cytoscape node fill color map attribute is used to color the nodes in eXamine according to gene expression score (task G1). The user therefore has the freedom to define the desired color map via Cytoscape. The user can invoke eXamine on the currently selected nodes via the eXamine control panel. There the user can select which categories to show as well as the number of sets per category. In addition, the user can specify that the Cytoscape selection should be updated to match the union or intersection of the selected sets in eXamine. This enables the use of eXamine with any kind of module extraction algorithm and/or filter method in Cytoscape, which includes manual node selection.

Results: a case study of US28 mediated signaling

We demonstrate how a domain expert can use eXamine by working out a case study in which a data set is re-analyzed (this work was done by the co-authors with biological expertise). While this data set has been studied extensively, it was possible to derive a new hypothesis via eXamine

The Human Cytomegalovirus (HCMV) is a highly-contagious herpes virus [41]. Infection with HCMV in healthy humans usually does not result in symptoms. However, in humans with a compromised immune system the virus is correlated with diseases such as hepatitis and retinitis [42]. In addition, HCMV gene products have been detected in various tumors even though HCMV is not considered to be an oncogenic virus. Experts therefore hypothesize that the virus may act as a stimulating factor during onset and development of cancer without being a root cause [43–45].

HCMV is responsible for the production of several viral G protein-coupled receptors (vGPCRs). Of these vGPCRs, US28 is the most studied and is characterized as chemokine sink [46]. Chemokines are signaling proteins that induce cell migration. Moreover, US28 hijacks the host cell’s signaling pathways, stimulates proliferative signaling pathways [47–51]. Previous studies focused on transcriptome analysis to evaluate pathways that are affected by US28. Differentially expressed genes involved in HCMV-induced disease symptoms were identified and related to known pathways [49, 50]. However, this analysis did not include network-based module extraction and enrichment.

To identify additional deregulated signaling due to US28, we analyzed the same data overlaid on the KEGG mouse network [8]. The network consisted of 3863 nodes and 29293 edges. Gene p-values, reflecting whether genes are significantly differentially expressed, were derived using RMA [52] and LIMMA [53]. Heinz [7], a tool for identifying differentially expressed modules, was then applied using a false discovery rate of 0.0007. This resulted in a module of 17 proteins. Finally, enrichment analysis using TopGO [54] was performed to annotate this module with enriched GO-terms and KEGG pathways (see Figure 8).

These data processing steps correspond to the initial steps in Figure 1. The subsequent analysis of the annotated module aims at obtaining new insights about US28-mediated signaling. The analysis follows the visual analytics cycle consisting of observation, knowledge, questions and exploration, finalized by a hypothesis. All analysis steps are shown in the screencast of Additional file 1.

C1 Two familiar pathways

Observation.

The KEGG pathway annotation sets show significant presence of Pathways in cancer and Phosphatidylinositol signaling (p-values of 5.6·10−6 and 1.0·10−6, respectively).

Knowledge.

An oncomodulatory role has been proposed for US28 [43–45], which coincides with the presence of Pathways in cancer and makes the genes annotated by this term of interest. Phosphatidylinositol signaling corresponds to previous work linking US28 to Phosphatidylinositol-mediated calcium responses [47, 55].

Question.

Which parts of the module are involved in Pathways in cancer and Phosphatidylinositol signaling?

Interaction.

Tag the Pathways in cancer and Phosphatidylinositol signaling annotation sets (see Figure 8(a)).

C2 Choosing sides

Observation.

Clear division of the module is apparent after tagging the two familiar pathways. Genes Arf6, Csnk2a1, Csnk2a1, Ipmk, Nr3c2 and Rock1 are not part of the pathways but have direct, unambiguous interactions with either of the pathways.

Knowledge.

Because of the known involvement of US28 in Phosphatidylinositol signaling, we do not focus on the genes of this pathway (Calm1..3, Plcb4, Pip5k1a), nor on the directly interacting genes (Arf6, Ipmk, Rock1). Instead, the Pathways in cancer genes Kras, Met, Figf, Hgf, Fgf7, Ctnnb1 and Tcf7l1, and directly interacting genes Nr3c2 and Csnk2a1 may lead to new insights in US28-mediated signaling and ultimately the oncomodulatory role of HCMV.

Question.

Do any of the aforementioned genes in or adjacent to Pathways in cancer lead to new insights in US28-mediated signaling?

Interaction.

Hover over the genes in and close to Pathways in cancer to determine mechanisms of interest.

C3 A twist of β -catenin

Observation.

The genes in Pathways in cancer can be divided roughly into two subsets: those that are annotated by growth-factor activity and those annotated by β -catenin binding (see Figure 8(b)). Csnk2a1, Tcf7l1 and Met are part of the latter annotation set, where Tcf7l1 and Csnk2a1 are down- and up-regulated, respectively. Expression of the neighboring Ctnnb1 (β-catenin) is up-regulated.

Knowledge.

β-catenin signaling results in elevated protein levels of the TCF/LEF transcription factor family that contains the protein encoded by Tcf7l1. Although Tcf7l1 is down-regulated, a recent study shows that this is not reflected at the protein level and that US28 induces β-catenin signaling [51]. In the same study, involvement of WNT/Frizzled via the canonical signaling pathway was ruled out and a hypothesis stating that US28-mediated signaling of β-catenin proceeds via ROCK1, which is also present in the module, was postulated.

Question.

Are there alternative mechanisms explaining the activation of β-catenin?

Interaction.

Tag the Growth factor activity annotation set (see Figure 8(b)).

C4 Growing knowledge

Observation.

Fgf, Hgf and Figf are annotated with Growth factor activity and connected to β-catenin via Met.

Knowledge.

MET is a receptor tyrosine kinase, whose only ligand is HGF. Therefore we can rule out the links from Met to Fgf and to Figf. In fact, these links are artifacts of how the mouse network was constructed from KEGG pathways. These artifacts often link whole groups of genes such as, in this case, growth factors to receptor tyrosine kinases.

Question.

Does the Hgf–Met axis relate to β-catenin activation?

Interaction.

Hover over Met and Ctnnb1 (β-catenin).

C5 New insights

Observation.

Met and β-catenin are both part of the Adherens junction pathway, as are Tcf7l1 and Csnk2a1 (see Figure 8(c)).

Knowledge.

Adherens junctions bind two cells together, keeping multiple cells in place. Alternative mechanisms have been described that explain β-catenin activation via the release of β-catenin from cell to cell adherens junctions (e.g. [56]). US28 promotes cell migration [57, 58], which causes the loss of cell to cell contacts with subsequent release of β-catenin into the cytoplasm. This may explain increased levels of β-catenin as found previously [51].

By requesting additional information for Adherens junction via eXamine, showing an external website by KEGG, we find an indirect connection between Met and β-catenin in the pathway (see Figure 10). Activation of MET via HGF mediates the release of β-catenin from adherens junctions, resulting in increased TCF/LEF levels [59, 60].

Figure 10
figure10

Connection between Met and β -catenin. Proteins that are associated to the selected Adherens junction at the left and corresponding KEGG pathway information at the right, where reactions catalyzed by module proteins are marked in red. Activation of MET by its ligand HGF results in the phosphorylation of β-catenin. This in turn results in its release from cadherin-complexes on the cell membrane into the cytoplasm.

Full size image

Hypothesis.

Combining this with the growth factor observations of C4 Growing knowledgeleads to the following hypothesis.

  • US28-mediated up-regulation of Hgf results in elevated levels of the corresponding HGF protein;

  • The subsequent activation of MET results in the release of β-catenin into the cytoplasm;

  • Subsequent translocation into the nucleus leads to enhanced TCF/LEF activation.

Synopsis

We are currently validating the hypothesis experimentally. Preliminary results indicate that the up-regulation of Hgf is indeed reflected at the protein level. Should this hypothesis turn out to be true, we would obtain crucial insights into one of the mechanisms by which the HCMV-encoded chemokine receptor US28 rewires cellular signaling. Ultimately, we would like to understand how this virus achieves its oncomodulatory role and how this can be disrupted.

Discussion

The analysis tasks described in the background section guided the design decisions that we have taken in the implementation of eXamine. These decisions are motivated via the analysis cycles of the US28 case study.

Overview.

The benefit of a spacious annotation set overview follows from the first cycle (C1 Two familiar pathways), in which the categorized, ranked, and legible annotation lists enable the fast recognition of two familiar and significantly represented pathways (task A1). Subsequent tagging of the two pathways reveals their module genes (task A2) and concisely drawn contours emphasize the division of the module into two parts and some additional genes that are not part of the pathways.

An annotation table, separate of the network, would not have made this division as apparent. The main reason is that annotation set transitions along gene interactions are not explicit in such a representation. In contrast, such cross-contour interaction links are clearly visible in eXamine (e.g. the transition from Kras in Pathways in cancer to Nr3c2 outside of Pathways in cancer).

Annotated genes.

The need to focus on specific genes and their properties appears in the second analysis cycle (C2 Choosing sides), in which genes of Pathways in cancer are inspected for annotations of interest (task G3). Highlighting annotations by hovering over genes enables fast identification of relevant annotations in the stable overview that oriented the analyst in C1 Two familiar pathways. Vice versa, hovering an annotation of interest (β -Catenin binding) confirms that it is shared by Csnk2a1, Tcf7l1, and Met (task G4). The same observations could have been made from an annotation table. However, the topological characteristics of these three genes would have been harder to discern, i.e., their direct interaction with Ctnnb1 (task G2). This also applies to other set visualizations without depiction of network topology, such as Venn or Euler diagrams, as shown in Figure 3(a) and (b). To make the topology of the gene interactions more explicit, a node-link visualization could be used. For example, Figure 3(c) shows the module laid out by one of the built-in force-directed layout algorithms of Cytoscape with all five annotation sets superimposed as BubbleSets. However, the structure of the annotation sets is hard to discern, and it is not immediately clear that nodes belonging to the β-catenin binding set (blue shape) form a proper subset of the Adherens junction set (yellow shape).

Integration.

The third cycle (C3 A twist of β -catenin) shows the importance of gene expression values (task G1), which is not limited to the interpretation of genes in isolation but along multiple genes, their interactions, and shared annotation sets. The importance of integrated support for all analysis tasks follows from the remaining cycles (C4 Growing knowledge-C5 New insights), where multiple deductions are made in succession via multiple tasks. Here, tagging relevant pathways enables the analyst to build up a context for making deductions.

Limitations.

eXamine is designed to accurately convey small and annotated modules, consisting of up to about thirty proteins and categories of up to about twenty annotations (note that these limits are not hard). The case study shows that common analysis tasks for these modules are covered. Scalability is a concern as our approach focuses on small modules to enable accurate depiction of sets contours; it is not possible to construct a comprehensive layout if the module consists of hundreds of proteins or if there are dozens of annotation sets to visualize at the same time. Both aspects make visual analysis ineffective. This is a natural limitation of any visualization approach based on node-link diagrams and set contours, however.

Our technique relies on a focus and context approach, in which the network and set system has been pruned down to the most relevant components first. Communicating small-scale information is given priority to support hypothesis generation at the level of individual proteins and their interactions, as follows from the targeted analysis tasks. Nonetheless, the tool is capable of visualizing modules of up to a hundred proteins, albeit with less legibility of interactions and annotations.

The integration of eXamine into Cytoscape mitigates many scalability issues. Cytoscape, for example, provides a global view of the network, in which the user can zoom in on smaller subnetworks for more in-depth analysis by eXamine. In addition, the integration into Cytoscape provides access to further analysis algorithms.

The extended SOM algorithm embeds an annotated module to reflect its topology, i.e., the distances between its proteins based on common interactions and annotations. This does not guarantee optimal aesthetics however, and unnecessary link and contour intersections can sometimes occur. The analysis tasks targeted by eXamine are not much hampered by such intersections since all interactions, annotations, and their interplay remain pronounced. However, to communicate analysis results, aesthetics might need further improvement. This could be done by weighing aesthetic criteria such as the number of intersections and shape complexity against each other, and formulating this as a combinatorial optimization problem. The associated algorithms [11] are often complex, and it is not so easy to integrate them into an interactive system.

Application to other domains.

eXamine is not limited to the analysis of enriched protein modules nor to data from the biological domain. It can be applied to any small network module that is accompanied by a set system, such as a social circle that consists of people, their relationships, and common interests.

Conclusions

We have proposed a visualization approach that enables the analysis of small and annotated network modules, and have implemented this in the Cytoscape app eXamine. Our approach displays sets as contours on top of a node-link layout. We have introduced an extension to the self-organizing maps algorithm to lay out module edges and annotation sets in a unified way. The added value of our approach has been demonstrated in a case study of a US28-mediated signaling module, in which a novel hypothesis about the way US28 induces β-catenin signaling has been derived.

Availability and requirements

Project name: eXamine Project homepage:http://apps.cytoscape.org/apps/examine Operating system(s): allProgramming language: JavaOther requirements: Cytoscape 3.xLicense: GPL2Any restrictions to use by non-academics: None

References

  1. 1.

    Alizadeh AA, Eisen MB, Davis RE, Ma C, Lossos IS, Rosenwald A, Boldrick JC, Sabet H, Tran T, Yu X, Powell JI, Yang L, Marti GE, Moore T, Hudson J, Lu L, Lewis DB, Tibshirani R, Sherlock G, Chan WC, Greiner TC, Weisenburger DD, Armitage JO, Warnke R, Levy R, Wilson W, Grever MR, Byrd JC, Botstein D, Brown PO, Staudt LM: Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling. Nature. 2000, 403 (6769): 503-511. 10.1038/35000501.

  2. 2.

    Golub TR, Slonim DK, Tamayo P, Huard C, Gaasenbeek M, Mesirov JP, Coller H, Loh ML, Downing JR, Caligiuri MA: Molecular classification of cancer class discovery and class prediction by gene expression monitoring. Science. 1999, 286 (5439): 531-537. 10.1126/science.286.5439.531.

  3. 3.

    van de Vijver MJ, He YD, van’t Veer LJ, Dai H, Hart AAM, Voskuil DW, Schreiber GJ, Peterse JL, Roberts C, Marton MJ, Parrish M, Atsma D, Witteveen A, Glas A, Delahaye L, van der Velde T, Bartelink H, Rodenhuis S, Rutgers ET, Friend SH, Bernards R: A gene-expression signature as a predictor of survival in breast cancer. N Engl J Med. 2002, 347 (25): 1999-2009. 10.1056/NEJMoa021967.

  4. 4.

    Tarca AL, Draghici S, Khatri P, Hassan SS, Mittal P, Kim CJ, Kusanovic JP, Romero R, Kim Js: A novel signaling pathway impact analysis. Bioinformatics. 2009, 25: 75-82. 10.1093/bioinformatics/btn577.

  5. 5.

    Vaske CJ, Benz SC, Sanborn JZ, Earl D, Szeto C, Zhu J, Haussler D, Stuart JM: Inference of patient-specific pathway activities from multi-dimensional cancer genomics data using PARADIGM. Bioinformatics. 2010, 26 (12): i237-i245. 10.1093/bioinformatics/btq182.

  6. 6.

    Ideker T, Ozier O, Schwikowski B, Siegel AF: Discovering regulatory and signalling circuits in molecular interaction networks. Bioinformatics. 2002, 18 (Suppl 1): S233-S240. 10.1093/bioinformatics/18.suppl_1.S233.

  7. 7.

    Dittrich MT, Klau GW, Rosenwald A, Dandekar T, Müller T: Identifying functional modules in protein-protein interaction networks: an integrated exact approach. Bioinformatics. 2008, 24 (13): i223-i231. 10.1093/bioinformatics/btn161.

  8. 8.

    Kanehisa M, Goto S: KEGG: Kyoto encyclopedia of genes and genomes. Nucleic Acids Res. 2000, 28: 27-30. 10.1093/nar/28.1.27.

  9. 9.

    Mitra K, Carvunis AR, Ramesh SK, Ideker T: Integrative approaches for finding modular structure in biological networks. Nat Rev Genet. 2013, 14 (10): 719-732. 10.1038/nrg3552.

  10. 10.

    Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, Cherry JM, Davis AP, Dolinski K, Dwight SS, Eppig JT, Harris MA, Hill DP, Issel-Tarver L, Kasarskis A, Lewis S, Matese JC, Richardson JE, Ringwald M, Rubin GM, Sherlock G: Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet. 2000, 25: 25-29. 10.1038/75556.

  11. 11.

    Battista G, Eades P, Tamassia R, Tollis I: Graph drawing: algorithms for the visualization of graphs. 1998, Upper Saddle River, NJ, USA: Prentice Hall PTR

  12. 12.

    Herman I, Melançon G, Marshall MS: Graph visualization and navigation in information visualization: A survey. IEEE Trans Vis Comput Graph. 2000, 6: 24-43. 10.1109/2945.841119.

  13. 13.

    von Landesberger T, Kuijper A, Schreck T, Kohlhammer J, van Wijk J, Fekete JD, Fellner D: Visual analysis of large graphs: state-of-the-art and future research challenges. Comput Graph Forum. 2011, 30 (6): 1719-1749. 10.1111/j.1467-8659.2011.01898.x.

  14. 14.

    Gehlenborg N, O’Donoghue SI, Baliga NS, Goesmann A, Hibbs MA, Kitano H, Kohlbacher O, Neuweger H, Schneider R, Tenenbaum D, Gavin AC: Visualization of omics data for systems biology. Nat Methods. 2010, 7 (3s): S56-S68. 10.1038/nmeth.1436.

  15. 15.

    Smooth ME, Ono K, Ruscheinski J, Wang PL, Ideker T: Cytoscape 2.8: new features for data integration and network visualization. Bioinformatics. 2011, 27 (3): 431-432. 10.1093/bioinformatics/btq675.

  16. 16.

    van Iersel MP, Kelder T, Pico AR, Hanspers K, Coort S, Conklin BR, Evelo C: Presenting and exploring biological pathways with PathVisio. BMC Bioinformatics. 2008, 9: 399-10.1186/1471-2105-9-399.

  17. 17.

    Venn and Euler diagrams. http://apps.cytoscape.org/apps/vennandeulerdiagrams.,

  18. 18.

    RBVI Cytoscape Plugins – Cytoscape group support. http://www.rbvi.ucsf.edu/cytoscape/groups.,

  19. 19.

    Bertault F, Eades P: Drawing Hypergraphs in the subset standard. Proceedings of the 8th International Symposium on Graph Drawing, Volume 1984 of Lecture Notes in Computer Science. 2001, Berlin, Heidelberg: Springer, 164-169.

  20. 20.

    Simonetto P, Auber D, Archambault D: Fully automatic visualisation of overlapping sets. Comput Graph Forum. 2009, 28 (3): 967-974. 10.1111/j.1467-8659.2009.01452.x.

  21. 21.

    Riche N, Dwyer T: Untangling Euler diagrams. IEEE Trans Vis Comput Graph. 2010, 16 (6): 1090-1099.

  22. 22.

    Alper B, Riche N, Ramos G, Czerwinski M: Design Study of LineSets, a Novel Set Visualization Technique. IEEE Trans Vis Comput Graph. 2011, 17 (12): 2259-2267.

  23. 23.

    Dinkla K, van Kreveld M, Speckmann B, Westenberg M: Kelp Diagrams Point Set Membership Visualization. Comput Graph Forum. 2012, 31 (3): 875-884.

  24. 24.

    Collins C, Penn G, Carpendale S: Bubble Sets: revealing set relations with Isocontours over existing visualizations. IEEE Trans Vis Comput Graph. 2009, 15 (6): 1009-1016.

  25. 25.

    Smith AM, Xu W, Sun Y, Faeder JR, Marai GE: RuleBender: integrated modeling, simulation and visualization for rule-based intracellular biochemistry. BMC Bioinformatics. 2012, 13 (Suppl 8): S3-10.1186/1471-2105-13-S8-S3.

  26. 26.

    Meulemans W, Riche NH, Speckmann B, Alper B, Dwyer T: KelpFusion: A Hybrid Set Visualization Technique. IEEE Trans Vis Comput Graph. 2013, 19 (11): 1846-1858.

  27. 27.

    Sugiyama K, Misue K: Visualization of structural information: automatic drawing of compound digraphs. IEEE Trans Syst Man Cybernet. 1991, 21 (4): 876-892. 10.1109/21.108304.

  28. 28.

    Shneiderman B, Aris A: Network visualization by semantic substrates. IEEE Trans Vis Comput Graph. 2006, 12 (5): 733-740.

  29. 29.

    Barsky A, Munzner T, Gardy J, Kincaid R: Cerebral: visualizing multiple experimental conditions on a graph with biological context. IEEE Trans Vis Comput Graph. 2008, 14 (6): 1253-1260.

  30. 30.

    Dwyer T, Marriott K, Schreiber F, Stuckey P, Woodward M, Wybrow M: Exploration of networks using overview+detail with constraint-based cooperative layout. IEEE Trans Vis Comput Graph. 2008, 14 (6): 1293-1300.

  31. 31.

    Gansner ER, Hu Y, Kobourov S: GMap: Visualizing graphs and clusters as maps. Pacific Visualization Symposium (PacificVis). 2010, IEEE, 201-208.

  32. 32.

    Fruchterman T, Reingold E: Graph drawing by force-directed placement. Softw: Practice Exper. 1991, 21 (11): 1129-1164. 10.1002/spe.4380211102.

  33. 33.

    Dwyer T, Marriott K, Stuckey P: Fast node overlap removal. Graph Drawing, Volume 3843 of Lecture Notes in Computer Science. 2006, Berlin, Germany: Springer Berlin Heidelberg, 153-164.

  34. 34.

    Kohonen T: The self-organizing map. Proc IEEE. 1990, 78 (9): 1464-1480. 10.1109/5.58325.

  35. 35.

    Vesanto J: SOM-based data visualization methods. Intell Data Anal. 1999, 3 (2): 111-126. 10.1016/S1088-467X(99)00013-X.

  36. 36.

    MacCallum R, Redmond S, Christophides G: An expression map for Anopheles gambiae. BMC Genomics. 2011, 12: 620-10.1186/1471-2164-12-620.

  37. 37.

    Frishman Y, Tal A: Online dynamic graph drawing. IEEE Trans Vis Comput Graph. 2008, 14 (4): 727-740.

  38. 38.

    de Berg M, Cheong O, van Kreveld M, Overmars M: Computational Geometry: Algorithms and Applications. 2008, Berlin, Heidelberg: Springer

  39. 39.

    Vivid Solutions: Java topology suite. http://www.vividsolutions.com/jts 2003,

  40. 40.

    Harrower M, Brewer C: ColorBrewer.org: An Online Tool for Selecting Colour Schemes for Maps. 2011, Chichester, UK: John Wiley & Sons, Ltd

  41. 41.

    Gandhi MK, Khanna R: Human cytomegalovirus: clinical aspects, immune regulation, and emerging treatments. Lancet Infect Dis. 2004, 4 (12): 725-738. 10.1016/S1473-3099(04)01202-2.

  42. 42.

    Söderberg-Nauclér C: Does cytomegalovirus play a causative role in the development of various inflammatory diseases and cancer?. J Intern Med. 2006, 259 (3): 219-246. 10.1111/j.1365-2796.2006.01618.x.

  43. 43.

    Cobbs CS, Harkins L, Samanta M, Gillespie GY, Bharara S, King PH, Nabors LB, Cobbs CG, Britt WJ: Human cytomegalovirus infection and expression in human malignant glioma. Cancer Res. 2002, 62 (12): 3347-3350.

  44. 44.

    Harkins L, Volk AL, Samanta M, Mikolaenko I, Britt WJ, Bland KI, Cobbs CS: Specific localisation of human cytomegalovirus nucleic acids and proteins in human colorectal cancer. Lancet. 2002, 360 (9345): 1557-1563. 10.1016/S0140-6736(02)11524-8.

  45. 45.

    JU V, H WD, Cinatl JJ: Oncomodulatory signals by regulatory proteins encoded by human cytomegalovirus: a novel role for viral infection in tumor progression. FEMS Microbiol Rev. 2004, 28: 59-77. 10.1016/j.femsre.2003.07.005.

  46. 46.

    Randolph-Habecker J, Rahill B, Torok-Storb B, Vieira J, Kolattukudy PE, Rovin BH, Sedmak DD: The expression of the cytomegalovirus chemokine receptor homolog US28 sequesters biologically active CC chemokines and alters IL-8 production. Cytokine. 2002, 19: 37-46. 10.1006/cyto.2002.0874.

  47. 47.

    Casarosa P, Bakker RA, Verzijl D, Navis M, Timmerman H, Leurs R, Smit MJ: Constitutive signaling of the human cytomegalovirus-encoded Chemokine receptor US28. J Biol Chem. 2001, 276 (2): 1133-1137. 10.1074/jbc.M008965200.

  48. 48.

    Maussang D, Verzijl D, van Walsum M, Leurs R, Holl J, Pleskoff O, Michel D, van Dongen GAMS, Smit MJ: Human cytomegalovirus-encoded chemokine receptor US28 promotes tumorigenesis. Proc Nat Acad Sci. 2006, 103 (35): 13068-13073. 10.1073/pnas.0604433103.

  49. 49.

    Maussang D, Langemeijer E, Fitzsimons CP, Stigter-van Walsum M, Dijkman R, Borg MK, Slinger E, Schreiber A, Michel D, Tensen CP, van Dongen GA, Leurs R, Smit MJ: The human cytomegalovirus-encoded Chemokine receptor US28 promotes angiogenesis and tumor formation via Cyclooxygenase-2. Cancer Res. 2009, 69 (7): 2861-2869. 10.1158/0008-5472.CAN-08-2487.

  50. 50.

    Slinger E, Maussang D, Schreiber A, Siderius M, Rahbar A, Fraile-Ramos A, Lira SA, Soderberg-Naucler C, Smit MJ: HCMV-Encoded Chemokine Receptor US28 mediates proliferative signaling through the IL-6-STAT3 axis. Sci Signal. 2010, 3 (133): ra58-10.1126/scisignal.2001180.

  51. 51.

    Langemeijer EV, Slinger E, de Munnik S, Schreiber A, Maussang D, Vischer H, Verkaar F, Leurs R, Siderius M, Smit MJ: Constitutiveβ-Catenin signaling by the viral Chemokine receptor US28. PLoS ONE. 2012, 7 (11): e48935-10.1371/journal.pone.0048935.

  52. 52.

    Gautier L, Cope L, Bolstad BM, Irizarry RA: affy—analysis of Affymetrix GeneChip data at the probe level. Bioinformatics. 2004, 20 (3): 307-315. 10.1093/bioinformatics/btg405.

  53. 53.

    Smyth G: limma: linear models for microarray data. Bioinformatics And Computational Biology Solutions Using R and Bioconductor, Statistics for Biology and Health. Edited by: Gentleman R, Carey V, Huber W, Irizarry R, Dudoit S. 2005, New York, NY, USA: Springer New York, 397-420.

  54. 54.

    Alexa A, Rahnenfuhrer J, Lengauer T: Improved scoring of functional groups from gene expression data by decorrelating GO graph structure. Bioinformatics. 2006, 22 (13): 1600-1607. 10.1093/bioinformatics/btl140.

  55. 55.

    Minisini R, Tulone C, Lüske A, Michel D, Mertens T, Gierschik P, Moepps B: Constitutive inositol phosphate formation in cytomegalovirus-infected human fibroblasts is due to expression of the chemokine receptor homologue pUS28. J Virol. 2003, 77 (8): 4489-4501. 10.1128/JVI.77.8.4489-4501.2003.

  56. 56.

    Zhurinsky J, Shtutman M, Ben-Ze’ev A: Differential mechanisms of LEF/TCF family-dependent transcriptional activation byβ-Catenin and Plakoglobin. Mol Cell Biol. 2000, 20 (12): 4238-4252. 10.1128/MCB.20.12.4238-4252.2000.

  57. 57.

    Streblow DN, Soderberg-Naucler C, Vieira J, Smith P, Wakabayashi E, Ruchti F, Mattison K, Altschuler Y, Nelson JA: The human cytomegalovirus chemokine receptor US28 mediates vascular smooth muscle cell migration. Cell. 1999, 99 (5): 511-520. 10.1016/S0092-8674(00)81539-1.

  58. 58.

    Streblow DN, Vomaske J, Smith P, Melnychuk R, Hall L, Pancheva D, Smit M, Casarosa P, Schlaepfer DD, Nelson JA: Human Cytomegalovirus Chemokine receptor US28-induced smooth muscle cell migration is mediated by focal adhesion kinase and Src. J Biol Chem. 2003, 278 (50): 50456-50465. 10.1074/jbc.M307936200.

  59. 59.

    Herynk MH, Tsan R, Radinsky R, Gallick GE: Activation of c-Met in colorectal carcinoma cells leads to constitutive association of tyrosine-phosphorylatedβ-catenin. Clin & Exp Metastasis. 2003, 20 (4): 291-300. 10.1023/A:1024024218529.

  60. 60.

    Purcell R, Childs M, Maibach R, Miles C, Turner C, Zimmermann A, Sullivan M: HGF/c-Met related activation of beta-catenin in hepatoblastoma. J Exp & Clin Cancer Res. 2011, 30: 96-10.1186/1756-9966-30-96.

Download references

Acknowledgements

Kasper Dinkla is supported by the Netherlands Organisation for Scientific Research (NWO) under project no. 612.001.004.

Author information

Affiliations

  1. Eindhoven University of Technology, Den Dolech 2, 5600 MB, Eindhoven, The Netherlands
    • Kasper Dinkla
    •  & Michel A Westenberg
  2. Life Sciences, Centrum Wiskunde & Informatica (CWI), Science Park 123, 1098, XG, Amsterdam, The Netherlands
    • Mohammed El-Kebir
    • , Cristina-Iulia Bucur
    •  & Gunnar W Klau
  3. VU University Amsterdam, De Boelelaan 1105, 1081, HV, Amsterdam, The Netherlands
    • Mohammed El-Kebir
    • , Cristina-Iulia Bucur
    • , Marco Siderius
    • , Martine J Smit
    •  & Gunnar W Klau
Authors
  1. Kasper Dinkla
    View author publications
    You can also search for this author in
  2. Mohammed El-Kebir
    View author publications
    You can also search for this author in
  3. Cristina-Iulia Bucur
    View author publications
    You can also search for this author in
  4. Marco Siderius
    View author publications
    You can also search for this author in
  5. Martine J Smit
    View author publications
    You can also search for this author in
  6. Michel A Westenberg
    View author publications
    You can also search for this author in
  7. Gunnar W Klau
    View author publications
    You can also search for this author in

Corresponding author

Correspondence to Michel A Westenberg.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

KD, MEK, MAW and GWK conceived the visual analysis technique. KD and MEK implemented eXamine. CIB, MS and MJS applied it to the US28 case study after instructions by MEK and GWK. KD, MEK, MAW and GWK drafted the manuscript. All authors read and approved the final manuscript.

Electronic supplementary material

12859_2014_6477_MOESM1_ESM.mp4

Additional file 1: Screencast. Screencast of interactive analysis in eXamine for the US28 case study. (MP4 13 MB)

Additional file 1: Screencast. Screencast of interactive analysis in eXamine for the US28 case study. (MP4 13 MB)

Authors’ original submitted files for images

Rights and permissions

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Dinkla, K., El-Kebir, M., Bucur, C. et al. eXamine: Exploring annotated modules in networks. BMC Bioinformatics 15, 201 (2014). https://doi.org/10.1186/1471-2105-15-201

Download citation

Keywords

  • Network analysis
  • Module
  • Set-based annotation
  • Visualization
  • Cytoscape

BMC Bioinformatics

ISSN: 1471-2105

Contact us