Algorithms, haplotypes and phylogenetic networks

Preface. Before I started my PhD in computational biology in 2005, I had never even heard of this term. Now, almost four years later, I think I have some idea of what is meant by it. One of the goals of my PhD was to explore different topics within computational biology and to see where the biggest opportunities for discrete/combinatorial mathematicians could be found. Roughly speaking, the first two years of my PhD I focussed mainly on problems related to haplotyping and genome rearrangements and the last two years on phylogenetic networks. I must say I really enjoyed learning so much about both mathematics and biology. It was especially amazing to learn how exact, theoretical mathematics can be used to solve complex, practical problems from biology. The topics I studied clearly show how extremely useful mathematics can be for biology. But I also learned that there are many more interesting topics in computational biology than the ones that I could study so far. The number of opportunities for discrete mathematicians is absolutely immense. I did not include my studies on genome rearrangements in this thesis, because my most interesting results [Hur07a; Hur07b] are not directly related to biology. This work is nevertheless interesting to mathematicians and I recommend them to read it. I can certainly conclude that also in this field there is a vast number of opportunities for mathematicians and that the topic genome rearrangements provides numerous beautiful mathematical problems. I could never have written this thesis without a great amount of help from many different people. I want to thank my supervisors Leen Stougie and Judith Keijsper for guiding me, for helping me, for correcting my mistakes, for supplying ideas and for the enjoyable time I had while working with them. I also want to thank the Dutch BSIK/BRICKS project for funding my research and Gerhard Woeginger for giving me the opportunity to work in his group and being my second promotor. I want to thank Jens Stoye and Julia Zakotnik for the work we did together and for the great time I had in Bielefeld. I want to thank Ferry Hagen and Teun Boekhout for helping me to make my work relevant for "real" biology. I also want to thank John Tromp, Rudi Cilibrasi, Cor Hurkens and all others I worked with during my PhD. I want to thank Erik de Vink and Mike Steel for reading and commenting my thesis. I want to thank my colleagues from the Combinatorial Optimisation group at the Technische Universiteit Eindhoven for the pleasant working conditions and the fun things we did besides work. I especially want to thank Matthias Mnich, not only a great colleague but also a good friend, for all his ideas, his humour and our good and fruitful cooperation. I also want to thank Steven Kelk. I must say that I was very lucky to work with Steven during my PhD. He introduced me to problems, had an enormous amount of ideas, found the critical mistakes in my proofs and made my PhD a success both in terms of results and in terms of enjoying work. Finally, I want to thank Conno Hendriksen and Bas Heideveld for assisting me during my PhD defence and I want to thank them and all my other friends and family for helping me with everything in my life but research

A list of parameterized problems in bioinformatics

In this report we present a list of problems that originated in bionformatics. Our aim is to collect information on such problems that have been analyzed from the point of view of Parameterized Complexity. For every problem we give its definition and biological motivation together with known complexity results.Postprint (published version

Introduction to the Minimum Rainbow Subgraph problem

Arisen from the Pure Parsimony Haplotyping problem in the bioinformatics, we developed the Minimum Rainbow Subgraph problem (MRS problem): Given a graph $G$, whose edges are coloured with $p$ colours. Find a subgraph $F\\\\subseteq G$ of $G$ of minimum order and with $p$ edges such that each colour occurs exactly once. We proved that this problem is NP-hard, and even APX-hard. Furthermore, we stated upper and lower bounds on the order of such minimum rainbow subgraphs. Several polynomial-time approximation algorithms concerning their approximation ratio and complexity were discussed. Therefore, we used Greedy approaches, or introduced the local colour density $\\\\lcd(T,S)$, giving a ratio on the number of colours and the number of vertices between two subgraphs $S,T\\\\subseteq G$ of $G$. Also, we took a closer look at graphs corresponding to the original haplotyping problem and discussed their special structure.:Mathematics and biology - having nothing in common? I. Going for a start 1. Introducing haplotyping 2. Becoming mathematical II. The MRS problem 3. The graph theoretical point of view 3.1. The MRS problem 3.2. The MRS problem on special graph classes 4. Trying to be not that bad 4.1. Greedy approaches 4.2. The local colour density 4.3. MaxNewColour 5. What is real data telling us? And the work goes on and on Bibliograph

AIRO 2016. 46th Annual Conference of the Italian Operational Research Society. Emerging Advances in Logistics Systems Trieste, September 6-9, 2016 - Abstracts Book

The AIRO 2016 book of abstract collects the contributions from the conference participants. The AIRO 2016 Conference is a special occasion for the Italian Operations Research community, as AIRO annual conferences turn 46th edition in 2016. To reflect this special occasion, the Programme and Organizing Committee, chaired by Walter Ukovich, prepared a high quality Scientific Programme including the first initiative of AIRO Young, the new AIRO poster section that aims to promote the work of students, PhD students, and Postdocs with an interest in Operations Research. The Scientific Programme of the Conference offers a broad spectrum of contributions covering the variety of OR topics and research areas with an emphasis on “Emerging Advances in Logistics Systems”. The event aims at stimulating integration of existing methods and systems, fostering communication amongst different research groups, and laying the foundations for OR integrated research projects in the next decade. Distinct thematic sections follow the AIRO 2016 days starting by initial presentation of the objectives and features of the Conference. In addition three invited internationally known speakers will present Plenary Lectures, by Gianni Di Pillo, Frédéric Semet e Stefan Nickel, gathering AIRO 2016 participants together to offer key presentations on the latest advances and developments in OR’s research

Extended Islands of Tractability for Parsimony Haplotyping

Parsimony haplotyping is the problem of finding a smallest size set of haplotypes that can explain a given set of genotypes. The problem is NP-hard, and many heuristic and approximation algorithms as well as polynomial-time solvable special cases have been discovered. We propose improved fixed-parameter tractability results with respect to the parameter “size of the target haplotype set ” k by presenting an O ∗ (k 4k)-time algorithm. This also applies to the practically important constrained case, where we can only use haplotypes from a given set. Furthermore, we show that the problem becomes polynomial-time solvable if the given set of genotypes is complete, i.e., contains all possible genotypes that can be explained by the set of haplotypes

The microbial ecology of Escherichia coli in the vertebrate gut.

Escherichia coli has a rich history as biology's favourite organism, driving advances across many fields. In the wild, E. coli often resides innocuously in the human and animal gut but is also a common pathogen linked to intestinal and extraintestinal infections and antimicrobial resistance. A literature review exposed gaps in our knowledge of the ecology and evolution of this organism in the vertebrate gut. I therefore investigated the genomic diversity and burden of antimicrobial resistance of E. coli in three vertebrate hosts from the Gambia. First, I explored the population structure of E. coli in non-human primates from the Gambia, where they interact with human communities. Here, I found strains closely related to those causing human extraintestinal infection, together with novel strains specific to the intestinal ecosystems of non-human primates. Next, I investigated the population structure of E. coli in backyard chickens and guinea fowl, which are commonly reared in Gambian homes as affordable sources of protein. I identified a clade of E. coli sequence type ST155 that includes closely related isolates from poultry and livestock from sub-Saharan Africa, suggesting that poultry and livestock exchange strains of E. coli on this continent. I compared the prevalence of antimicrobial resistance genes in E. coli isolates from Gambian poultry to that seen in poultry isolates from around the world. Finally, I used genomic analysis to shed light on the relative contributions of immigration and within-host evolution in the generation of diversity among commensal strains of E. coli in the guts of healthy children from rural Gambia. In closing, I discuss the implications and prospects of these findings