PhD Studentship at Babraham - Systems Pharmacology Models of Druggable Targets and Disease Mechanisms
Our friendly neighbours at The Babraham Institute are looking for a PhD candidate to work on systems pharmacology models, as part of a collaboration between the Le Novère (Babraham), the Hermjakob (EMBL-EBI) and the pharmaceutical company GlaxoSmithKline. The Le Novère group uses quantitative computational models to understand cellular and molecular processes, and develop community services that facilitate research in computational systems biology (http://lenoverelab.org).
One of the major challenges of drug discovery is to demonstrate the efficacy of a potential new
drug. This goes beyond the development of a potent molecule - it also implies a good
understanding of the biological context, how it relates to a particular disease, and the drug's
mechanism of action. The availability of relevant Systems Pharmacology models can therefore have
a significant impact. The most comprehensive repository of Systems Biology models in machine
readable language is BioModels Database, created by Le Novère and maintained at the EBI. In spite
of its extensive collection, BioModels Database only covers a fraction of the Systems Pharmacology
models described in the literature. In addition, no analysis has been performed on how they map
to druggable targets and/or disease mechanisms.
The candidate will:
The candidate must have an extensive knowledge of molecular biology and pharmacology, and solid basis in numerical analysis and statistics. Advanced familiarity with data representation and programming skills will also be desirable.
For any further information or to express interest, please contact Nicolas Le Novère (n.lenovere (at) gmail.com)
The candidate will:
- Use state-of-the-art text-mining methods to extract and analyse the space of Systems Pharmacology models currently described in the literature, with particular emphasis to their relevance to druggable targets and disease mechanisms;
- Identify the models offering the best opportunities for the discovery of new drugs, and incorporate them into BioModels Database;
- Explore and assess the applicability of those models to real drug development cases, evaluating their quality, advantages, caveats, overlaps, gaps and impact on the demonstration of drug efficacy against specific indications.
The candidate must have an extensive knowledge of molecular biology and pharmacology, and solid basis in numerical analysis and statistics. Advanced familiarity with data representation and programming skills will also be desirable.
- Thiele I et al. A community-driven global reconstruction of human metabolism. Nat Biotechnol. 2013 Mar 3. Online advance publication.
- Cucurull-Sanchez L et al. Relevance of systems pharmacology in drug discovery. Drug Discov Today. 2012 17: 665-670
- Le Novère N et al. BioModels Database: a free, centralized database of curated, published, quantitative kinetic models of biochemical and cellular systems. Nucleic Acids Res. 2006 34: D689-D691.
For any further information or to express interest, please contact Nicolas Le Novère (n.lenovere (at) gmail.com)