Graph based gene/protein prediction and clustering over uncertain medical databases.

Clustering over protein or gene data is now a popular issue in biomedical databases. In general, large sets of gene tags are clustered using high computation techniques over gene or protein distributed data. Most of the traditional clustering techniques are based on subspace, hierarchical and partitioning feature extraction. Various clustering techniques have been proposed in the literature with different cluster measures, but their performance is limited due to spatial noise and uncertainty. In this paper, an improved graph-based clustering technique is proposed for the generation of efficient gene or protein clusters over uncertain and noisy data. The proposed graph-based visualization can effectively identify different types of genes or proteins along with relational attributes. Experimental results show that the proposed graph model more effectively clusters complex gene or protein data when compared with conventional clustering approaches

Scalable Edge Clustering of Dynamic Graphs via Weighted Line Graphs

Timestamped relational datasets consisting of records between pairs of entities are ubiquitous in data and network science. For applications like peer-to-peer communication, email, social network interactions, and computer network security, it makes sense to organize these records into groups based on how and when they are occurring. Weighted line graphs offer a natural way to model how records are related in such datasets but for large real-world graph topologies the complexity of building and utilizing the line graph is prohibitive. We present an algorithm to cluster the edges of a dynamic graph via the associated line graph without forming it explicitly. We outline a novel hierarchical dynamic graph edge clustering approach that efficiently breaks massive relational datasets into small sets of edges containing events at various timescales. This is in stark contrast to traditional graph clustering algorithms that prioritize highly connected community structures. Our approach relies on constructing a sufficient subgraph of a weighted line graph and applying a hierarchical agglomerative clustering. This work draws particular inspiration from HDBSCAN. We present a parallel algorithm and show that it is able to break billion-scale dynamic graphs into small sets that correlate in topology and time. The entire clustering process for a graph with $O(10 \text{ billion})$ edges takes just a few minutes of run time on 256 nodes of a distributed compute environment. We argue how the output of the edge clustering is useful for a multitude of data visualization and powerful machine learning tasks, both involving the original massive dynamic graph data and/or the non-relational metadata. Finally, we demonstrate its use on a real-world large-scale directed dynamic graph and describe how it can be extended to dynamic hypergraphs and graphs with unstructured data living on vertices and edges.Comment: 26 pages, 15 figure

Bayesian nonparametric clusterings in relational and high-dimensional settings with applications in bioinformatics.

Recent advances in high throughput methodologies offer researchers the ability to understand complex systems via high dimensional and multi-relational data. One example is the realm of molecular biology where disparate data (such as gene sequence, gene expression, and interaction information) are available for various snapshots of biological systems. This type of high dimensional and multirelational data allows for unprecedented detailed analysis, but also presents challenges in accounting for all the variability. High dimensional data often has a multitude of underlying relationships, each represented by a separate clustering structure, where the number of structures is typically unknown a priori. To address the challenges faced by traditional clustering methods on high dimensional and multirelational data, we developed three feature selection and cross-clustering methods: 1) infinite relational model with feature selection (FIRM) which incorporates the rich information of multirelational data; 2) Bayesian Hierarchical Cross-Clustering (BHCC), a deterministic approximation to Cross Dirichlet Process mixture (CDPM) and to cross-clustering; and 3) randomized approximation (RBHCC), based on a truncated hierarchy. An extension of BHCC, Bayesian Congruence Measuring (BCM), is proposed to measure incongruence between genes and to identify sets of congruent loci with identical evolutionary histories. We adapt our BHCC algorithm to the inference of BCM, where the intended structure of each view (congruent loci) represents consistent evolutionary processes. We consider an application of FIRM on categorizing mRNA and microRNA. The model uses latent structures to encode the expression pattern and the gene ontology annotations. We also apply FIRM to recover the categories of ligands and proteins, and to predict unknown drug-target interactions, where latent categorization structure encodes drug-target interaction, chemical compound similarity, and amino acid sequence similarity. BHCC and RBHCC are shown to have improved predictive performance (both in terms of cluster membership and missing value prediction) compared to traditional clustering methods. Our results suggest that these novel approaches to integrating multi-relational information have a promising future in the biological sciences where incorporating data related to varying features is often regarded as a daunting task

Non-parametric Bayesian modeling of complex networks

Modeling structure in complex networks using Bayesian non-parametrics makes it possible to specify flexible model structures and infer the adequate model complexity from the observed data. This paper provides a gentle introduction to non-parametric Bayesian modeling of complex networks: Using an infinite mixture model as running example we go through the steps of deriving the model as an infinite limit of a finite parametric model, inferring the model parameters by Markov chain Monte Carlo, and checking the model's fit and predictive performance. We explain how advanced non-parametric models for complex networks can be derived and point out relevant literature

Relational visual cluster validity

The assessment of cluster validity plays a very important role in cluster analysis. Most commonly used cluster validity methods are based on statistical hypothesis testing or finding the best clustering scheme by computing a number of different cluster validity indices. A number of visual methods of cluster validity have been produced to display directly the validity of clusters by mapping data into two- or three-dimensional space. However, these methods may lose too much information to correctly estimate the results of clustering algorithms. Although the visual cluster validity (VCV) method of Hathaway and Bezdek can successfully solve this problem, it can only be applied for object data, i.e. feature measurements. There are very few validity methods that can be used to analyze the validity of data where only a similarity or dissimilarity relation exists – relational data. To tackle this problem, this paper presents a relational visual cluster validity (RVCV) method to assess the validity of clustering relational data. This is done by combining the results of the non-Euclidean relational fuzzy c-means (NERFCM) algorithm with a modification of the VCV method to produce a visual representation of cluster validity. RVCV can cluster complete and incomplete relational data and adds to the visual cluster validity theory. Numeric examples using synthetic and real data are presente

Transforming Graph Representations for Statistical Relational Learning

Relational data representations have become an increasingly important topic due to the recent proliferation of network datasets (e.g., social, biological, information networks) and a corresponding increase in the application of statistical relational learning (SRL) algorithms to these domains. In this article, we examine a range of representation issues for graph-based relational data. Since the choice of relational data representation for the nodes, links, and features can dramatically affect the capabilities of SRL algorithms, we survey approaches and opportunities for relational representation transformation designed to improve the performance of these algorithms. This leads us to introduce an intuitive taxonomy for data representation transformations in relational domains that incorporates link transformation and node transformation as symmetric representation tasks. In particular, the transformation tasks for both nodes and links include (i) predicting their existence, (ii) predicting their label or type, (iii) estimating their weight or importance, and (iv) systematically constructing their relevant features. We motivate our taxonomy through detailed examples and use it to survey and compare competing approaches for each of these tasks. We also discuss general conditions for transforming links, nodes, and features. Finally, we highlight challenges that remain to be addressed