相关论文: On the maximum agreement subtree conjecture for ba…
Extending some properties from the Euclidean plane to any normed plane, we show the validity of the Monma-Paterson-Suri-Yao algorithm for finding the maximum-weighted spanning tree of a set of $n$ points, where the weight of an edge is the…
We prove the Tree Alternative Conjecture for the topological minor relation: letting $[T]$ denote the equivalence class of $T$ under the topological minor relation we show that: $|[T]| = 1$ or $|[T]|\geq \aleph_0$ and $\forall r\in V(T)$,…
We compute the magnitude (an isometric invariant of metric spaces) of compact $\mathbb{R}$-trees and show that it equals $1 + L/2$, where $L \in [0, \infty]$ denotes the total length. Although length is the only geometric invariant captured…
A subtree of a tree is any induced subgraph that is again a tree (i.e., connected). The mean subtree order of a tree is the average number of vertices of its subtrees. This invariant was first analyzed in the 1980s by Jamison. An intriguing…
We consider two varieties of labeled rooted trees, and the probability that a vertex chosen from all vertices of all trees of a given size uniformly at random has a given rank. We prove that this probability converges to a limit as the tree…
We give a necessary and sufficient condition for the maximum multiplicity of a root of the matching polynomial of a tree to be equal to the minimum number of vertex disjoint paths needed to cover it.
Applying a method to reconstruct a phylogenetic tree from random data provides a way to detect whether that method has an inherent bias towards certain tree `shapes'. For maximum parsimony, applied to a sequence of random 2-state data, each…
Tree balance plays an important role in different research areas like theoretical computer science and mathematical phylogenetics. For example, it has long been known that under the Yule model, a pure birth process, imbalanced trees are…
In this note, we obtain an upper bound on the maximum number of distinct non-empty palindromes in starlike trees. This bound implies, in particular, that there are at most $4n$ distinct non-empty palindromes in a starlike tree with three…
Let $T$ be a weighted tree. The weight of a subtree $T_1$ of $T$ is defined as the product of weights of vertices and edges of $T_1$. We obtain a linear-time algorithm to count the sum of weights of subtrees of $T$. As applications, we…
The Maximum (Minimum) Leaf Spanning Tree problem asks for a spanning tree with the largest (smallest) number of leaves. As spanning trees are often computed using graph search algorithms, it is natural to restrict this problem to the set of…
We consider NCA labeling schemes: given a rooted tree $T$, label the nodes of $T$ with binary strings such that, given the labels of any two nodes, one can determine, by looking only at the labels, the label of their nearest common…
A tanglegram consists of two rooted binary trees with the same number of leaves and a perfect matching between the leaves of the trees. Given a size-$n$ tanglegram, i.e., a tanglegram for two trees with $n$ leaves, a multiset of induced…
A graph $G=(V,E)$ is called 1-planar if it admits a drawing in the plane such that each edge is crossed at most once. In this paper, we study bipartite $1$-planar graphs with prescribed numbers of vertices in partite sets. Bipartite…
We define a notion of substitution on colored binary trees that we call substreetution. We show that a fixed point by a substreetution may be (or not) almost periodic, thus the closure of the orbit under $\mathbb{F}_2^+$-action may (or not)…
We introduce a model of tree-rooted planar maps weighted by their number of $2$-connected blocks. We study its enumerative properties and prove that it undergoes a phase transition. We give the distribution of the size of the largest…
Two results (together with their relatively elementary proofs) are presented. The first one presents the upper boundary on the number of spanning trees in a finite planar multigraph, proving that the complexity (the number of spanning…
Estimating phylogenetic trees, which depict the relationships between different species, from aligned sequence data (such as DNA, RNA, or proteins) is one of the main aims of evolutionary biology. However, tree reconstruction criteria like…
The tree-metric theorem provides a necessary and sufficient condition for a dissimilarity matrix to be a tree metric, and has served as the foundation for numerous distance-based reconstruction methods in phylogenetics. Our main result is…
We prove that if every subgraph of a graph $G$ has a balanced separation of order at most $a$ then $G$ has treewidth at most $15a$. This establishes a linear dependence between the treewidth and the separation number.