相关论文: The Distribution of the Deepest Leaves in Binary T…
We study the growth of a time-ordered rooted tree by probabilistic attachment of new vertices to leaves. We construct a likelihood function of the leaves based on the connectivity of the tree. We take such connectivity to be induced by the…
Despite the latest prevailing success of deep neural networks (DNNs), several concerns have been raised against their usage, including the lack of intepretability the gap between DNNs and other well-established machine learning models, and…
An m-extracting procedure produces unbiased random bits from a loaded dice with m faces. A binarization takes inputs from an m-faced dice and produce bit sequences to be fed into a (binary) extracting procedure to obtain random bits. Thus,…
It follows from a classical result of Jordan that every tree with maximum degree at most $r$ containing a vertex set labeled by $[n]$, has a single-edge cut which separates two subsets $A,B \subset [n]$ for which $\min\{|A|,|B|\} \ge…
The height of a random PATRICIA tree built from independent, identically distributed infinite binary strings with arbitrary diffuse probability distribution $\mu$ on $\{0,1\}^\mathbb{N}$ is studied. We show that the expected height grows…
If trees are constructed from a pure birth process and one defines the depth of a leaf to be the number of edges to its root, it is known that the variance in the depth of a randomly selected leaf of a randomly selected tree grows linearly…
The coverage depth problem in DNA data storage is about computing the expected number of reads needed to recover all encoded strands. Given a generator matrix of a linear code, this quantity equals the expected number of randomly drawn…
To each generic complex polynomial $p(z)$ there is associated a labeled binary tree (here referred to as a "lemniscate tree") that encodes the topological type of the graph of $|p(z)|$. The branching structure of the lemniscate tree is…
We obtain new non-asymptotic tail bounds for the height of uniformly random trees with a given degree sequence, simply generated trees and conditioned Bienaym\'e trees (the family trees of branching processes), in the process settling three…
Recently, there has been interest in extending long-known results about the multispecies coalescent tree to other models of gene trees. Results about the gene duplication and loss (GDL) tree have mathematical proofs, including species tree…
We consider special cases of the two tree degree sequences problem. We show that if two tree degree sequences do not have common leaves then they always have edge-disjoint caterpillar realizations. By using a probabilistic method, we prove…
Rooted binary perfect phylogenies provide a generalization of rooted binary unlabeled trees in which each leaf is assigned a positive integer value that corresponds in a biological setting to the count of the number of indistinguishable…
We prove that every tree of maximum degree $\Delta$ with $\ell$ leaves contains paths between leaves of at least $\log_{\Delta-1}((\Delta-2)\ell)$ distinct lengths. This settles in a strong form a conjecture of Narins, Pokrovskiy and…
An identifying code $C$ of a graph $G$ is a dominating set of $G$ such that any two distinct vertices of $G$ have distinct closed neighbourhoods within $C$. These codes have been widely studied for over two decades. We give an improvement…
Since the 90's, several authors have studied a probability distribution on the set of Boolean functions on $n$ variables induced by some probability distributions on formulas built upon the connectors $And$ and $Or$ and the literals…
The study of Locally Checkable Labelings (LCLs) has led to a remarkably precise characterization of the distributed time complexities that can occur on bounded-degree trees. A central feature of this complexity landscape is the existence of…
Phylogenetic trees are leaf-labelled trees used to model the evolution of species. In practice it is not uncommon to obtain two topologically distinct trees for the same set of species, and this motivates the use of distance measures to…
The evolution of aligned DNA sequence sites is generally modeled by a Markov process operating along the edges of a phylogenetic tree. It is well known that the probability distribution on the site patterns at the tips of the tree…
A layerwise search in a split-by-edges tree (as defined by Br{\ae}ndeland, 2015) of agiven graph produces a maximum independent set in exponential time. A depth-first search produces an independent set, which may or may not be a maximum, in…
Ge, Rusjan, and Zweifel (J. Stat. Phys. 59, 1265 (1990)) introduced a binary tree which represents all the periodic windows in the chaotic regime of iterated one-dimensional unimodal maps. We consider the scaling behavior in a modified tree…