Search bioRxiv⌕ Search

Biology subjects

Coti, C.

Publications and source records attributed to Coti, C..

2 recordsLinked to original sources

FASTiso: Fast Algorithm on Search state Tree for subgraph ISOmorphism in graphs of any size and density

Subgraph isomorphism is a fundamental combinatorial problem that involves finding one or more occurrences of a pattern graph within a target graph. It arises in a wide range of application domains, including biology, chemistry, social network analysis, and pattern recognition. Although subgraph isomorphism is NP-complete in the general case, many exact algorithms allow it to be solved in practice on many instances. However, the increasing size and structural diversity of graph datasets continue to pose significant challenges in terms of robustness and scalability. In this article, we propose FASTiso, an exact subgraph isomorphism algorithm that emphasizes a strong consistency between the variable ordering strategy and the pruning rules used during search. This design enables a unified exploitation of structural information throughout the exploration process, leading to improved efficiency and stable performance across heterogeneous graph structures. An extensive experimental evaluation on widely used synthetic and real-world benchmarks shows that FASTiso consistently outperforms reference solvers such as VF3, VF3L, and RI, and achieves competitive performance compared to constraint programming-based approaches (Glasgow, PathLad+), while outperforming them on most datasets. The results further demonstrate that FASTiso remains highly efficient on small instances and scales well to large graphs, while maintaining a lower memory footprint than most evaluated solvers. The peak memory usage is 7.74 GB for FASTiso, 36.19 GB for PathLad+, over 500 GB for Glasgow, 9.62 GB for VF3/VF3L, and 4.31 GB for RI. FASTiso code is available at https://gitlab.info.uqam.ca/cbe/fastiso as a C++ implementation, a Python module, and an integration within an extended version of NetworkX. The implementations support simple graphs and multigraphs, directed or undirected, with labels on nodes, edges, or both.

bioinformatics↗

Parallel maximal common subgraphs with labels for molecular biology

Advances in graph algorithmics have allowed in-depth study of many natural objects from molecular biology or chemistry to social networks. Particularly in molecular biology and cheminformatics, understanding complex structures by identifying conserved sub-structures is a key milestone towards the artificial design of novel components with specific functions. Given a dataset of structures, we are interested in identifying all maximum common connected partial subgraphs between each pair of graphs, a task notoriously NP-Hard. In this work, we present parallel algorithms over shared and distributed memory to enumerate all maximal connected common sub-graphs between pairs of arbitrary multi-directed graphs with labels on their edges. We offer an implementation of these methods and evaluate their performance on the non-redundant dataset of all known RNA 3D structures. We show that we can compute the exact results in a reasonable time for each pairwise comparison while taking into account a much more diverse set of interactions--resulting in much denser graphs--resulting in an order of magnitude more conserved modules. All code is available at https://gitlab.info.uqam.ca/cbe/pasigraph and results in the branch results.

bioinformatics↗