Lagrangian relaxation applied to sparse global network alignment

  • Authors:
  • Mohammed El-Kebir;Jaap Heringa;Gunnar W. Klau

  • Affiliations:
  • Centrum Wiskunde & Informatica, Life Sciences Group, Amsterdam, The Netherlands and Centre for Integrative Bioinformatics VU, VU University Amsterdam and Netherlands Institute for Systems Biol ...;Centre for Integrative Bioinformatics VU, VU University Amsterdam, Amsterdam, The Netherlands and Netherlands Institute for Systems Biology and Netherlands Bioinformatics Centre;Centrum Wiskunde & Informatica, Life Sciences Group, Amsterdam, The Netherlands and Netherlands Institute for Systems Biology

  • Venue:
  • PRIB'11 Proceedings of the 6th IAPR international conference on Pattern recognition in bioinformatics
  • Year:
  • 2011

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Abstract

Data on molecular interactions is increasing at a tremendous pace, while the development of solid methods for analyzing this network data is lagging behind. This holds in particular for the field of comparative network analysis, where one wants to identify commonalities between biological networks. Since biological functionality primarily operates at the network level, there is a clear need for topology-aware comparison methods. In this paper we present a method for global network alignment that is fast and robust, and can flexibly deal with various scoring schemes taking both node-to-node correspondences as well as network topologies into account. It is based on an integer linear programming formulation, generalizing the well-studied quadratic assignment problem. We obtain strong upper and lower bounds for the problem by improving a Lagrangian relaxation approach and introduce the software tool NATALIE 2.0, a publicly available implementation of our method. In an extensive computational study on protein interaction networks for six different species, we find that our new method outperforms alternative state-of-the-art methods with respect to quality and running time. An extended version of this paper including proofs and pseudo code is available at http://arxiv.org/pdf/1108.4358v1.