arXiv subjects

Andreas Spillner

Publications and source records attributed to Andreas Spillner.

13 recordsLinked to original sources

arXiv2026

EL-Shellability of the poset of ranked cactuses

Recently the poset of ranked cactuses $(\mathfrak{P}(X),\preceq)$ was introduced. For a finite set $X$, this poset consists of a set $\mathfrak{P}(X)$ of certain collections of ordered pairs of subsets of $X$ together with an ordering $\preceq$ that is similar to the refinement ordering of partitions of a finite set. In addition, the maximal chains in this poset correspond to binary ranked cactuses, a fact which can be used to construct the so-called space of equidistant cactuses. In this paper, we show that the poset of ranked cactuses is EL-shellable. As a consequence we also show that the proper part of the link of the origin of the space of equidistant cactuses has the homotopy type of a wedge of spheres.

math.CO↗

arXiv2025

Labeling and folding multi-labeled trees

In 1989 Erd\H{o}s and Sz\'ekely showed that there is a bijection between (i) the set of rooted trees with $n+1$ vertices whose leaves are bijectively labeled with the elements of $[\ell]=\{1,2,\dots,\ell\}$ for some $\ell \leq n$, and (ii) the set of partitions of $[n]=\{1,2,\dots,n\}$. They established this via a labeling algorithm based on the anti-lexicographic ordering of non-empty subsets of $[n]$ which extends the labeling of the leaves of a given tree to a labeling of all of the vertices of that tree. In this paper, we generalize their approach by developing a labeling algorithm for multi-labeled trees, that is, rooted trees whose leaves are labeled by positive integers but in which distinct leaves may have the same label. In particular, we show that certain orderings of the set of all finite, non-empty multisets of positive integers can be used to characterize partitions of a multiset that arise from labelings of multi-labeled trees. As an application, we show that the recently introduced class of labelable phylogenetic networks is precisely the class of phylogenetic networks that are stable relative to the so-called folding process on multi-labeled trees. We also give a bijection between the labelable phylogenetic networks with leaf-set $[n]$ and certain partitions of multisets.

cs.DM↗

arXiv2025

Subtree Distances, Tight Spans and Diversities

Metric embeddings are central to metric theory and its applications. Here we consider embeddings of a different sort: maps from a set to subsets of a metric space so that distances between points are approximated by minimal distances between subsets. Our main result is a characterization of when a set of distances $d(x,y)$ between elements in a set $X$ have a subtree representation, a real tree $T$ and a collection $\{S_x\}_{x \in X}$ of subtrees of~$T$ such that $d(x,y)$ equals the length of the shortest path in~$T$ from a point in $S_x$ to a point in $S_y$ for all $x,y \in X$. The characterization was first established for {\em finite} $X$ by Hirai (2006) using a tight span construction defined for distance spaces, metric spaces without the triangle inequality. To extend Hirai's result beyond finite $X$ we establish fundamental results of tight span theory for general distance spaces, including the surprising observation that the tight span of a distance space is hyperconvex. We apply the results to obtain the first characterization of when a diversity -- a generalization of a metric space which assigns values to all finite subsets of $X$, not just to pairs -- has a tight span which is tree-like.

math.MG↗

arXiv2024

Spaces of ranked tree-child networks

Ranked tree-child networks are a recently introduced class of rooted phylogenetic networks in which the evolutionary events represented by the network are ordered so as to respect the flow of time. This class includes the well-studied ranked phylogenetic trees (also known as ranked genealogies). An important problem in phylogenetic analysis is to define distances between phylogenetic trees and networks in order to systematically compare them. Various distances have been defined on ranked binary phylogenetic trees, but very little is known about comparing ranked tree-child networks. In this paper, we introduce an approach to compare binary ranked tree-child networks on the same leaf set that is based on a new encoding of such networks that is given in terms of a certain partially ordered set. This allows us to define two new spaces of ranked binary tree-child networks. The first space can be considered as a generalization of the recently introduced space of ranked binary phylogenetic trees whose distance is defined in terms of ranked nearest neighbor interchange moves. The second space is a continuous space that captures all equidistant tree-child networks and generalizes the space of ultrametric trees. In particular, we show that this continuous space is a so-called CAT(0)-orthant space which, for example, implies that the distance between two equidistant tree-child networks can be efficiently computed.

q-bio.PE↗

arXiv2024

Phylogenetic diversity indices from an affine and projective viewpoint

Phylogenetic diversity indices are commonly used to rank the elements in a collection of species or populations for conservation purposes. The derivation of these indices is typically based on some quantitative description of the evolutionary history of the species in question, which is often given in terms of a phylogenetic tree. Both rooted and unrooted phylogenetic trees can be employed, and there are close connections between the indices that are derived in these two different ways. In this paper, we introduce more general phylogenetic diversity indices that can be derived from collections of subsets (clusters) and collections of bipartitions (splits) of the given set of species. Such indices could be useful, for example, in case there is some uncertainty in the topology of the tree being used to derive a phylogenetic diversity index. As well as characterizing some of the indices that we introduce in terms of their special properties, we provide a link between cluster-based and split-based phylogenetic diversity indices that uses a discrete analogue of the classical link between affine and projective geometry. This provides a unified framework for many of the various phylogenetic diversity indices used in the literature based on rooted and unrooted phylogenetic trees, generalizations and new proofs for previous results concerning tree-based indices, and a way to define some new phylogenetic diversity indices that naturally arise as affine or projective variants of each other.

q-bio.PE↗

arXiv2021

The space of equidistant phylogenetic cactuses

We introduce and investigate the space of \emph{equidistant} $X$-\emph{cactuses}. These are rooted, arc weighted, phylogenetic networks with leaf set $X$, where $X$ is a finite set of species, and all leaves have the same distance from the root. The space contains as a subset the space of ultrametric trees on $X$ that was introduced by Gavryushkin and Drummond. We show that equidistant-cactus space is a CAT(0)-metric space which implies, for example, that there are unique geodesic paths between points. As a key step to proving this, we present a combinatorial result concerning \emph{ranked} rooted $X$-cactuses. In particular, we show that such networks can be encoded in terms of a pairwise compatibility condition arising from a poset of collections of pairs of subsets of $X$ that satisfy certain set-theoretic properties. As a corollary, we also obtain an encoding of ranked, rooted $X$-trees in terms of partitions of $X$, which provides an alternative proof that the space of ultrametric trees on $X$ is CAT(0). As with spaces of phylogenetic trees, we expect that our results should provide the basis for and new directions in performing statistical analyses for collections of phylogenetic networks with arc lengths.

q-bio.PE↗

arXiv2021

Phylogenetic consensus networks: Computing a consensus of 1-nested phylogenetic networks

An important and well-studied problem in phylogenetics is to compute a \emph{consensus tree} so as to summarize the common features within a collection of rooted phylogenetic trees, all whose leaf-sets are bijectively labeled by the same set~(X) of species. More recently, however, it has become of interest to find a consensus for a collection of more general, rooted directed acyclic graphs all of whose sink-sets are bijectively labeled by~(X), so called rooted \emph{phylogenetic networks}. These networks are used to analyse the evolution of species that cross with one another, such as plants and viruses. In this paper, we introduce an algorithm for computing a consensus for a collection of so-called 1-\emph{nested} phylogenetic networks. Our approach builds on a previous result by Rosell\'o et al. that describes an encoding for any 1-nested phylogenetic network in terms of a collection of ordered pairs of subsets of (X).More specifically, we characterize those collections of ordered pairs that arise as the encoding of some 1-nested phylogenetic network, and then use this characterization to compute a \emph{consensus network} for a collection of~$t$ 1-nested networks in $O(t|X|^2+|X|^3)$ time. Applying our algorithm to a collection of phylogenetic trees yields the well-known majority rule consensus tree. Our approach leads to several new directions for futurework, and we expect that it should provide a useful new tool to help understand complex evolutionary scenarios.

q-bio.PE↗

arXiv2019

Order distances and split systems

Given a distance $D$ on a finite set $X$ with $n$ elements, it is interesting to understand how the ranking $R_x = z_1,z_2,\dots,z_n$ obtained by ordering the elements in $X$ according to increasing distance $D(x,z_i)$ from $x$, varies with different choices of $x \in X$. The order distance $O_{p,q}(D)$ is a distance on $X$ associated to $D$ which quantifies these variations, where $q \geq \frac{p}{2} > 0$ are parameters that control how ties in the rankings are handled. The order distance $O_{p,q}(D)$ of a distance $D$ has been intensively studied in case $D$ is a treelike distance (that is, $D$ arises as the shortest path distances in an edge-weighted tree with leaves labeled by $X$), but relatively little is known about properties of $O_{p,q}(D)$ for general $D$. In this paper we study the order distance for various types of distances that naturally generalize treelike distances in that they can be generated by split systems, i.e. they are examples of so-called $l_1$-distances. In particular we show how and to what extent properties of the split systems associated to the distances $D$ that we study can be used to infer properties of $O_{p,q}(D)$.

cs.DM↗

arXiv2017

UPGMA and the normalized equidistant minimum evolution problem

UPGMA (Unweighted Pair Group Method with Arithmetic Mean) is a widely used clustering method. Here we show that UPGMA is a greedy heuristic for the normalized equidistant minimum evolution (NEME) problem, that is, finding a rooted tree that minimizes the minimum evolution score relative to the dissimilarity matrix among all rooted trees with the same leaf-set in which all leaves have the same distance to the root. We prove that the NEME problem is NP-hard. In addition, we present some heuristic and approximation algorithms for solving the NEME problem, including a polynomial time algorithm that yields a binary, rooted tree whose NEME score is within O(log^2 n) of the optimum. We expect that these results to eventually provide further insights into the behavior of the UPGMA algorithm.

q-bio.PE↗

arXiv2015

When can splits be drawn in the plane?

Split networks are a popular tool for the analysis and visualization of complex evolutionary histories. Every collection of splits (bipartitions) of a finite set can be represented by a split network. Here we characterize which collection of splits can be represented using a planar split network. Our main theorem links these collections of splits with oriented matroids and arrangements of lines separating points in the plane. As a consequence of our main theorem, we establish a particularly simple characterization of maximal collections of these splits.

q-bio.PE↗

arXiv2014

Searching for Realizations of Finite Metric Spaces in Tight Spans

An important problem that commonly arises in areas such as internet traffic-flow analysis, phylogenetics and electrical circuit design, is to find a representation of any given metric $D$ on a finite set by an edge-weighted graph, such that the total edge length of the graph is minimum over all such graphs. Such a graph is called an optimal realization and finding such realizations is known to be NP-hard. Recently Varone presented a heuristic greedy algorithm for computing optimal realizations. Here we present an alternative heuristic that exploits the relationship between realizations of the metric $D$ and its so-called tight span $T_D$. The tight span $T_D$ is a canonical polytopal complex that can be associated to $D$, and our approach explores parts of $T_D$ for realizations in a way that is similar to the classical simplex algorithm. We also provide computational results illustrating the performance of our approach for different types of metrics, including $l_1$-distances and two-decomposable metrics for which it is provably possible to find optimal realizations in their tight spans.

math.MG↗

arXiv2012

Recognizing Treelike k-Dissimilarities

A k-dissimilarity D on a finite set X, |X| >= k, is a map from the set of size k subsets of X to the real numbers. Such maps naturally arise from edge-weighted trees T with leaf-set X: Given a subset Y of X of size k, D(Y) is defined to be the total length of the smallest subtree of T with leaf-set Y . In case k = 2, it is well-known that 2-dissimilarities arising in this way can be characterized by the so-called "4-point condition". However, in case k > 2 Pachter and Speyer recently posed the following question: Given an arbitrary k-dissimilarity, how do we test whether this map comes from a tree? In this paper, we provide an answer to this question, showing that for k >= 3 a k-dissimilarity on a set X arises from a tree if and only if its restriction to every 2k-element subset of X arises from some tree, and that 2k is the least possible subset size to ensure that this is the case. As a corollary, we show that there exists a polynomial-time algorithm to determine when a k-dissimilarity arises from a tree. We also give a 6-point condition for determining when a 3-dissimilarity arises from a tree, that is similar to the aforementioned 4-point condition.

math.MG↗

arXiv2009

Untangling a Planar Graph

A straight-line drawing $δ$ of a planar graph $G$ need not be plane, but can be made so by \emph{untangling} it, that is, by moving some of the vertices of $G$. Let shift$(G,δ)$ denote the minimum number of vertices that need to be moved to untangle $δ$. We show that shift$(G,δ)$ is NP-hard to compute and to approximate. Our hardness results extend to a version of \textsc{1BendPointSetEmbeddability}, a well-known graph-drawing problem. Further we define fix$(G,δ)=n-shift(G,δ)$ to be the maximum number of vertices of a planar $n$-vertex graph $G$ that can be fixed when untangling $δ$. We give an algorithm that fixes at least $\sqrt{((\log n)-1)/\log \log n}$ vertices when untangling a drawing of an $n$-vertex graph $G$. If $G$ is outerplanar, the same algorithm fixes at least $\sqrt{n/2}$ vertices. On the other hand we construct, for arbitrarily large $n$, an $n$-vertex planar graph $G$ and a drawing $δ_G$ of $G$ with fix$(G,δ_G) \le \sqrt{n-2}+1$ and an $n$-vertex outerplanar graph $H$ and a drawing $δ_H$ of $H$ with fix$(H,δ_H) \le 2 \sqrt{n-1}+1$. Thus our algorithm is asymptotically worst-case optimal for outerplanar graphs.

cs.CG↗