Alexandru I. Tomescu

Sebastian Schmidt, Juha Harviainen, Corentin Moumard et al.

Bidirected graphs are a common generalisation of directed graphs where arcs can also be incoming to both their incident nodes, or outgoing from both their incident nodes. Such arcs allow a walk to change direction. Some algorithms can easily be adapted from directed graphs to bidirected graphs, such as shortest path algorithms. These adaptions are already used in practice, and implicitly use the graph doubling technique to apply an algorithm for directed graphs to bidirected graphs. In other cases, the applicability of graph doubling is not that obvious. For example, superbubbles and their generalisation to bidirected graphs ultrabubbles. Ultrabubbles are a common structure in bidirected biological graphs which carries biological meaning, but also functions as a nested clustering method, since an ultrabubble is separated by only two nodes from the rest of the graph. There is an existing method that enumerates a structure similar to ultrabubbles by enumerating (weak) superbubbles in the doubled graph. However, the literature does not make any direct connection between superbubbles and ultrabubbles except that a superbubble is an ultrabubble in a directed graph. Only a partial result connecting superbubbles and ultrabubbles exists by Harviainen et al. (2026). Graph doubling on the other hand maintains connectivity, and allows to draw a direct connection between ultrabubbles and weak superbubbles. This results in the first linear-time reduction-based algorithm for computing ultrabubbles on any bidirected graph. Together with the fact that graph doubling is already used implicitly in simple cases, our result motivates that graph doubling is a powerful yet simple technique to apply algorithms for directed graphs to bidirected graphs.

Francisco Sena, Aleksandr Politov, Corentin Moumard et al.

A fundamental algorithmic problem in computational biology is to find all subgraphs of a given type (superbubbles, snarls, and ultrabubbles) in a directed or bidirected input graph. These correspond to regions of genetic variation and are useful in analyzing collections of genomes. We present the first linear-time algorithms for identifying all snarls and all ultrabubbles, resolving problems open since 2018. The algorithm for snarls relies on a new linear-size representation of all snarls with respect to the number of vertices in the graph. We employ the well-known SPQR-tree decomposition, which encodes all 2-separators of a biconnected graph. After several dynamic-programming-style traversals of this tree, we maintain key properties (such as acyclicity) that allow us to decide whether a given 2-separator defines a subgraph to be reported. A crucial ingredient for linear-time complexity is that acyclicity of linearly many subgraphs can be tested simultaneously via the problem of computing all arcs in a directed graph whose removal renders it acyclic (so-called feedback arcs). As such, we prove a fundamental result for bidirected graphs, that may be of independent interest: all feedback arcs can be computed in linear time for tipless bidirected graphs, while in general this is at least as hard as matrix multiplication, assuming the k-Clique Conjecture. Our results form a unified framework that also yields a completely different linear-time algorithm for finding all superbubbles. Although some of the results are technically involved, the underlying ideas are conceptually simple, and may extend to other bubble-like subgraphs. More broadly, our work contributes to the theoretical foundations of computational biology and advances a growing line of research that uses SPQR-tree decompositions as a general tool for designing efficient algorithms, beyond their traditional role in graph drawing.