January 2012 - BBClist - maillist.psb.ugent.be

Bioinformatics position at Keygene, Wageningen
by Antoine Janssen 18 Jan '12

18 Jan '12

Dear collegues, Please find attached an ad for a bioinformatics position at Keygene. I would very much appreciate if you could forward it to your contacts. Thanks a lot for your help! Antoine Janssen Team Leader Bioinformatics [cid:imageb6d6f3.jpg@2a262fe6.cad54c8d] Keygene N.V. P.O. Box 216 6700 AE Wageningen The Netherlands Tel. (+31) 317 46 68 66 Fax. (+31) 317 42 49 39 Web: http://www.keygene.com<http://www.keygene.com/> The information contained in this message, and attachments if any, may be privileged and/or confidential and is intended to be received only by persons entitled to receive such information. Use of any part of this message and/or its attachments if any, in any other way than as explicitly stated by the sender is strictly prohibited. Should you receive this message unintentionally please notify the sender immediately, and delete it together with all attachments, if any. Thank you. The transmission of messages and/or information via the Internet is not secured and may be intercepted by third parties. KeyGene assumes no liability for any damage caused by any unintentional disclosure and/or use of the content of this message and attachments if any.

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Postdoc Position in Structural BioInformatics
by Marianne Rooman 09 Jan '12

09 Jan '12

Postdoc Position in Structural BioInformatics Starting date: between February 2012 and October 2012 Duration: 2 years Location : Genomic and Structural BioInformatics Unit, BioSystems, BioModeling & BioProcesses Department, Université Libre de Bruxelles, Belgium Subject: Development of computational tools for the rational design of modified proteins The ideal candidate should have experience in structural bioinformatics, in particular in the design and development of knowledge-based approaches for predicting the structure, stability, interactions or function of a protein from its sequence, preferentially in C programming language, or in the applications of such approaches to systems of biological or medical interest. The candidate should not have been domiciled in Belgium the last two years. Contact: Please send your applications with cover letter, full CV and the names and email addresses of two contact persons for reference letters to Marianne Rooman (mrooman(a)ulb.ac.be)

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mini-workshop on gene network inference, ULg, January 9, 10-12am
by Pierre Geurts 03 Jan '12

03 Jan '12

Dear Colleagues, The Systems and modeling research unit and the GIGA thematic research unit in Systems Biology and Chemical biology have the pleasure to invite you to the following two seminars on gene network inference: Speaker: Robert Küffner, Ludwig-Maximilians-Universität München, Munich, Germany Title: Solutions and Practical Problems in Gene Regulatory Network Inference Date and place: Monday January, 9th 10:00am, Room R7, Institut Montefiore, Sart Tilman, B28, Liège Speaker: Christophe Ambroise, Laboratoire Statistique et Génome, Université d'Évry Val d'Essonne Title: Inferring Sparse Gaussian Graphical Models for Biological Network Date and place: Monday January, 9th 11:00am, Room R7, Institut Montefiore, Sart Tilman, B28, Liège The seminars will be followed in the afternoon by Vân Anh Huynh-Thu's PhD defense: Title: Machine learning-based feature ranking: Statistical interpretation and gene network inference Date and place: Monday January 9th, 2:30pm, Room R3, Institut Montefiore, Sart Tilman, B28, Liège Abstracts and address below. With my best wishes for 2012, Pierre Geurts -- PLACE: Institut Montefiore, Sart Tilman, B28, Liège http://www.montefiore.ulg.ac.be/location.php ABSTRACTS: Speaker: Robert Küffner, Ludwig-Maximilians-Universität München, Munich, Germany Title: Solutions and Practical Problems in Gene Regulatory Network Inference Abstract: The inference of gene regulatory networks from mRNA expression data is characterized by the development of many different approaches with their specific performances, data requirements, and inherent biases. The recent community-wide DREAM challenge conducted a large assessment of inference approaches. The accuracy of predictions was evaluated against experimentally supported interactions in the procaryote model organism E. coli, the eucaryote model organism S. cerevisiae and in silico target systems. Further analysis revealed not only which inference strategies are particularly successful but also which kind of specific information was utilized from the different types of experimental measurements. The challenge evaluation also revealed several weaknesses and limitations of current methods for the generation of artificial datasets as well as the state of the art inference methods. For instance, none of the examined approaches was able to achieve robust predictions from S. cerevisiae data. ----------- Speaker: Christophe Ambroise, Laboratoire Statistique et Génome, Université d'Évry Val d'Essonne Title: Inferring Sparse Gaussian Graphical Models for Biological Network Abstract: Gaussian Graphical Models provide a convenient framework for representing dependencies between variables. In this framework, a set of variables is represented by an undirected graph, where vertices correspond to variables, and an edge connects two vertices if the corresponding pair of variables are dependent, conditional on the remaining ones. Recently, this tool has received a high interest for the discovery of biological networks by l1-penalization of the model likelihood. In this presentation, we introduce various ways of inferring sparse co-expression networks based on partial correlation coefficients from either steady-state or time-course transcriptomic data. All proposals search for a latent structure of the network to drive the selection of edges through an adaptive l1-penalization of the model likelihood. We focus on inference from samples collected in different experimental conditions and therefore not identically distributed. ----------- Speaker: Vân Anh Huynh-Thu, University of Liège Title: Machine learning-based feature ranking: Statistical interpretation and gene network inference Abstract: Machine learning techniques, and in particular supervised learning methods, are nowadays widely used in bioinformatics. Two prominent applications that we target specifically in this thesis are biomarker discovery and regulatory network inference. These two problems are commonly addressed through the use of feature ranking methods that order the input features of a supervised learning problem from the most to the less relevant for predicting the output. This thesis presents, on the one hand, methodological contributions around machine learning-based feature ranking techniques and on the other hand, more applicative contributions on gene regulatory network inference. Our methodological contributions focus on the problem of selecting truly relevant features from machine learning-based feature rankings. Unlike the p-values returned by univariate tests, relevance scores derived from machine learning techniques to rank the features are usually not statistically interpretable. This lack of interpretability makes the identification of the truly relevant features among the top-ranked ones a very difficult task and hence prevents the wide adoption of these methods by practitioners. Our first contribution in this field concerns a procedure, based on permutation tests, that estimates for each subset of top-ranked features the probability for that subset to contain at least one irrelevant feature (called CER for "conditional error rate"). As a second contribution, we performed a large-scale evaluation of several, existing or novel, procedures, including our CER method, that all replace the original relevance scores with measures that can be interpreted in a statistical way. These procedures, which were assessed on several artificial and real datasets, differ greatly in terms of computing times and the tradeoff they achieve in terms of false positives and false negatives. Our experiments also clearly highlight that using model performance as a criterion for feature selection is often counter-productive. The problem of gene regulatory network inference can be formulated as several feature selection problems, each one aiming at discovering the regulators of one target gene. Within this family of methods, we developed the GENIE3 algorithm that exploits feature rankings derived from tree-based ensemble methods to infer gene networks from steady-state gene expression data. In a second step, we derived two extensions of GENIE3 that aim to infer regulatory networks from other types of data. The first extension exploits expression data provided by time course experiments, while the second extension is related to genetical genomics datasets, which contain expression data together with information about genetic markers. GENIE3 was best performer in the DREAM4 In Silico Multifactorial challenge in 2009 and in the DREAM5 Network Inference challenge in 2010, and its extensions perform very well compared to other methods on several artificial datasets.

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