Reconstructing fully-resolved trees from triplet cover distances

It is a classical result that any finite tree with positively weighted edges, and without vertices of degree 2, is uniquely determined by the weighted path distance between each pair of leaves. Moreover, it is possible for a (small) strict subset L of leaf pairs to suffice for reconstructing the tree and its edge weights, given just the distances between the leaf pairs in L. It is known that any set L with this property for a tree in which all interior vertices have degree 3 must form a cover for T {that is, for each interior vertex v of T, L must contain a pair of leaves from each pair of the three components of T ̶ v. Here we provide a partial converse of this result by showing that if a set L of leaf pairs forms a cover of a certain type for such a tree T then T and its edge weights can be uniquely determined from the distances between the pairs of leaves in L. Moreover, there is a polynomial-time algorithm for achieving this reconstruction. The result establishes a special case of a recent question concerning `triplet covers', and is relevant to a problem arising in evolutionary genomics

Distinguished minimal topological lassos

The ease with which genomic data can now be generated using Next Generation Sequencing technologies combined with a wealth of legacy data holds great promise for exciting new insights into the evolutionary relationships between and within the kingdoms of life. At the sub-species level (e.g. varieties or strains) certain edge weighted rooted trees with leaf set the set $X$ of organisms under consideration are often used to represent them. Called Dendrograms, it is well-known that they can be uniquely reconstructed from distances provided all distances on $X$ are known. More often than not, real biological datasets do not satisfy this assumption implying that the sought after dendrogram need not be uniquely determined anymore by the available distances with regards to topology, edge-weighting, or both. To better understand the structural properties a set \cL\subseteq {X\choose 2} has to satisfy to overcome this problem, various types of lassos have been introduced. Here, we focus on the question of when a lasso uniquely determines the topology of a dendrogram, that is, it is a topological lasso for it's underlying tree. We show that any set-inclusion minimal topological lasso for such a tree $T$ can be transformed into a structurally nice minimal topological lasso for $T$. Calling such a lasso a distinguished minimal topological lasso for $T$ we characterize them in terms of the novel concept of a cluster marker map for $T$. In addition, we present novel results concerning the heritability of such lassos in the context of the subtree and supertree problems

Local and Global Explanations of Agent Behavior: Integrating Strategy Summaries with Saliency Maps

With advances in reinforcement learning (RL), agents are now being developed in high-stakes application domains such as healthcare and transportation. Explaining the behavior of these agents is challenging, as the environments in which they act have large state spaces, and their decision-making can be affected by delayed rewards, making it difficult to analyze their behavior. To address this problem, several approaches have been developed. Some approaches attempt to convey the $\textit{global}$ behavior of the agent, describing the actions it takes in different states. Other approaches devised $\textit{local}$ explanations which provide information regarding the agent's decision-making in a particular state. In this paper, we combine global and local explanation methods, and evaluate their joint and separate contributions, providing (to the best of our knowledge) the first user study of combined local and global explanations for RL agents. Specifically, we augment strategy summaries that extract important trajectories of states from simulations of the agent with saliency maps which show what information the agent attends to. Our results show that the choice of what states to include in the summary (global information) strongly affects people's understanding of agents: participants shown summaries that included important states significantly outperformed participants who were presented with agent behavior in a randomly set of chosen world-states. We find mixed results with respect to augmenting demonstrations with saliency maps (local information), as the addition of saliency maps did not significantly improve performance in most cases. However, we do find some evidence that saliency maps can help users better understand what information the agent relies on in its decision making, suggesting avenues for future work that can further improve explanations of RL agents

A matroid associated with a phylogenetic tree

A (pseudo-)metric D on a finite set X is said to be a `tree metric' if there is a finite tree with leaf set X and non-negative edge weights so that, for all x,y ∈X, D(x,y) is the path distance in the tree between x and y. It is well known that not every metric is a tree metric. However, when some such tree exists, one can always find one whose interior edges have strictly positive edge weights and that has no vertices of degree 2, any such tree is 13; up to canonical isomorphism 13; uniquely determined by D, and one does not even need all of the distances in order to fully (re-)construct the tree's edge weights in this case. Thus, it seems of some interest to investigate which subsets of X, 2 suffice to determine (`lasso') these edge weights. In this paper, we use the results of a previous paper to discuss the structure of a matroid that can be associated with an (unweighted) X-tree T defined by the requirement that its bases are exactly the `tight edge-weight lassos' for T, i.e, the minimal subsets of X, 2 that lasso the edge weights of T

Spaces of phylogenetic networks from generalized nearest-neighbor interchange operations

Phylogenetic networks are a generalization of evolutionary or phylogenetic trees that are used to represent the evolution of species which have undergone reticulate evolution. In this paper we consider spaces of such networks defined by some novel local operations that we introduce for converting one phylogenetic network into another. These operations are modeled on the well-studied nearest-neighbor interchange (NNI) operations on phylogenetic trees, and lead to natural generalizations of the tree spaces that have been previously associated to such operations. We present several results on spaces of some relatively simple networks, called level-1 networks, including the size of the neighborhood of a fixed network, and bounds on the diameter of the metric defined by taking the smallest number of operations required to convert one network into another.We expect that our results will be useful in the development of methods for systematically searching for optimal phylogenetic networks using, for example, likelihood and Bayesian approaches