Multi-hop assortativities for networks classification

Several social, medical, engineering and biological challenges rely on discovering the functionality of networks from their structure and node metadata, when is available. For example, in chemoinformatics one might want to detect whether a molecule is toxic based on structure and atomic types, or discover the research field for scientific collaboration networks. Existing techniques rely on counting or measuring structural patterns that are known to show large variations from network to network, such as number of triangles, or the assortativity of node metadata. We introduce the concept of multi-hop assortativity, that captures the similarity of node situated at the extremities of a randomly selected path of a given length. We show that multi-hop assortativity unifies various existing concepts and offers a versatile family of fingerprints to characterize networks. These fingerprints allow in turn to recover the functionalities of a network, with the help of the machine learning toolbox. Our method is evaluated empirically on established social and chemoinformatic network benchmarks. Results reveal that our assortativity based features are competitive providing highly accurate results often outperforming state of the art methods for the network classification task

Dynamics Based Features For Graph Classification

Numerous social, medical, engineering and biological challenges can be framed as graph-based learning tasks. Here, we propose a new feature based approach to network classification. We show how dynamics on a network can be useful to reveal patterns about the organization of the components of the underlying graph where the process takes place. We define generalized assortativities on networks and use them as generalized features across multiple time scales. These features turn out to be suitable signatures for discriminating between different classes of networks. Our method is evaluated empirically on established network benchmarks. We also introduce a new dataset of human brain networks (connectomes) and use it to evaluate our method. Results reveal that our dynamics based features are competitive and often outperform state of the art accuracies.