Gerth Stølting Brodal

Bio: Gerth Stølting Brodal is an academic researcher from Aarhus University. The author has contributed to research in topics: Data structure & Priority queue. The author has an hindex of 39, co-authored 166 publications receiving 4420 citations. Previous affiliations of Gerth Stølting Brodal include National Research Foundation of South Africa & Max Planck Society.

A Simple Greedy Algorithm for Dynamic Graph Orientation.

Abstract: Graph orientations with low out-degree are one of several ways to efficiently store sparse graphs. If the graphs allow for insertion and deletion of edges, one may have to flip the orientation of some edges to prevent blowing up the maximum out-degree. We use arboricity as our sparsity measure. With an immensely simple greedy algorithm, we get parametrized trade-off bounds between out-degree and worst case number of flips, which previously only existed for amortized number of flips. We match the previous best worst-case algorithm (in $$\mathcal {O}\left( \log n\right) $$ flips) for almost all values of arboricity and beat it for either constant or super-logarithmic arboricity. We also match a previous best amortized result for at least logarithmic arboricity, and give the first results with worst-case $$\mathcal {O}\left( 1\right) $$ and $$\mathcal {O}\left( \sqrt{\log n}\right) $$ flips nearly matching out-degree bounds to their respective amortized solutions.

The ComBack method: extending hash compaction with backtracking

Abstract: This paper presents the ComBack method for explicit state space exploration. The ComBack method extends the well-known hash compaction method such that full coverage of the state space is guaranteed. Each encountered state is mapped into a compressed state descriptor (hash value) as in hash compaction. The method additionally stores for each state an integer representing the identity of the state and a backedge to a predecessor state. This allows hash collisions to be resolved on-the-fly during state space exploration using backtracking to reconstruct the full state descriptors when required for comparison with newly encountered states. A prototype implementation of the ComBack method is used to evaluate the method on several example systems and compare its performance to related methods. The results show a reduction in memory usage at an acceptable cost in exploration time.

A Communication Complexity Proof that Symmetric Functions have Logarithmic Depth

Abstract: We present a direct protocol with logarithmic communication that finds an element in the symmetric difference of two sets of different size. This yields a simple proof that symmetric functions have logarithmic circuit depth.

Dynamic Planar Convex Hull with Optimal Query Time and O(log n log log n) Update Time

Abstract: The dynamic maintenance of the convex hull of a set of points in the plane is one of the most important problems in computational geometry. We present a data structure supporting point insertions in amortized O(log n · log log log n) time, point deletions in amortized O(log n · log log n) time, and various queries about the convex hull in optimal O(log n) worst-case time. The data structure requires O(n) space. Applications of the new dynamic convex hull data structure are improved deterministic algorithms for the k-level problem and the red-blue segment intersection problem where all red and all blue segments are connected.

Computing the quartet distance between evolutionary trees of bounded degree

Abstract: We present an algorithm for calculating the quartet distance between two evolutionary trees of bounded degree on a common set of n species. The previous best algorithm has running time O(d2n2) when considering trees, where no node is of more than degree d. The algorithm developed herein has running time O(d9n logn)) which makes it the first algorithm for computing the quartet distance between non-binary trees which has a sub-quadratic worst case running time.

Application of Phylogenetic Networks in Evolutionary Studies

Abstract: The evolutionary history of a set of taxa is usually represented by a phylogenetic tree, and this model has greatly facilitated the discussion and testing of hypotheses. However, it is well known that more complex evolutionary scenarios are poorly described by such models. Further, even when evolution proceeds in a tree-like manner, analysis of the data may not be best served by using methods that enforce a tree structure but rather by a richer visualization of the data to evaluate its properties, at least as an essential first step. Thus, phylogenetic networks should be employed when reticulate events such as hybridization, horizontal gene transfer, recombination, or gene duplication and loss are believed to be involved, and, even in the absence of such events, phylogenetic networks have a useful role to play. This article reviews the terminology used for phylogenetic networks and covers both split networks and reticulate networks, how they are defined, and how they can be interpreted. Additionally, the article outlines the beginnings of a comprehensive statistical framework for applying split network methods. We show how split networks can represent confidence sets of trees and introduce a conservative statistical test for whether the conflicting signal in a network is treelike. Finally, this article describes a new program, SplitsTree4, an interactive and comprehensive tool for inferring different types of phylogenetic networks from sequences, distances, and trees.

FastTree: Computing Large Minimum Evolution Trees with Profiles instead of a Distance Matrix

Abstract: Gene families are growing rapidly, but standard methods for inferring phylogenies do not scale to alignments with over 10,000 sequences. We present FastTree, a method for constructing large phylogenies and for estimating their reliability. Instead of storing a distance matrix, FastTree stores sequence profiles of internal nodes in the tree. FastTree uses these profiles to implement Neighbor-Joining and uses heuristics to quickly identify candidate joins. FastTree then uses nearest neighbor interchanges to reduce the length of the tree. For an alignment with N sequences, L sites, and a different characters, a distance matrix requires O(N2) space and O(N2L) time, but FastTree requires just O(NLa + N) memory and O(Nlog (N)La) time. To estimate the tree's reliability, FastTree uses local bootstrapping, which gives another 100-fold speedup over a distance matrix. For example, FastTree computed a tree and support values for 158,022 distinct 16S ribosomal RNAs in 17 h and 2.4 GB of memory. Just computing pairwise Jukes–Cantor distances and storing them, without inferring a tree or bootstrapping, would require 17 h and 50 GB of memory. In simulations, FastTree was slightly more accurate than Neighbor-Joining, BIONJ, or FastME; on genuine alignments, FastTree's topologies had higher likelihoods. FastTree is available at http://microbesonline.org/fasttree.

Fast Tree: Computing Large Minimum-Evolution Trees with Profiles instead of a Distance Matrix

Abstract: Gene families are growing rapidly, but standard methods for inferring phylogenies do not scale to alignments with over 10,000 sequences. We present FastTree, a method for constructing large phylogenies and for estimating their reliability. Instead of storing a distance matrix, FastTree stores sequence profiles of internal nodes in the tree. FastTree uses these profiles to implement neighbor-joining and uses heuristics to quickly identify candidate joins. FastTree then uses nearest-neighbor interchanges to reduce the length of the tree. For an alignment with N sequences, L sites, and a different characters, a distance matrix requires O(N^2) space and O(N^2 L) time, but FastTree requires just O( NLa + N sqrt(N) ) memory and O( N sqrt(N) log(N) L a ) time. To estimate the tree's reliability, FastTree uses local bootstrapping, which gives another 100-fold speedup over a distance matrix. For example, FastTree computed a tree and support values for 158,022 distinct 16S ribosomal RNAs in 17 hours and 2.4 gigabytes of memory. Just computing pairwise Jukes-Cantor distances and storing them, without inferring a tree or bootstrapping, would require 17 hours and 50 gigabytes of memory. In simulations, FastTree was slightly more accurate than neighbor joining, BIONJ, or FastME; on genuine alignments, FastTree's topologies had higher likelihoods. FastTree is available at http://microbesonline.org/fasttree.

BOLD : The Barcode of Life Data System (www.barcodinglife.org)

Abstract: The Barcode of Life Data System ( BOLD ) is an informatics workbench aiding the acquisition, storage, analysis and publication of DNA barcode records. By assembling molecular, morphological and distributional data, it bridges a traditional bioinformatics chasm. BOLD is freely available to any researcher with interests in DNA barcoding. By providing specialized services, it aids the assembly of records that meet the standards needed to gain BARCODE designation in the global sequence databases. Because of its web-based delivery and flexible data security model, it is also well positioned to support projects that involve broad research alliances. This paper provides a brief introduction to the key elements of BOLD , discusses their functional capabilities, and concludes by examining computational resources and future prospects.