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		<title>NBIC Latest positions</title>
		<link>http://nbic.roquin.net/about-nbic/jobspositions/</link>
		<description>The 20 most recent positions available at NBIC</description>
		<language>en</language>
		
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                        <title><![CDATA[HBO (B.Sc.) Bioinformatician ]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/hbo-bsc-bioinformatician-1/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/hbo-bsc-bioinformatician-1/</guid>
                        <pubDate>Wed, 03 Mar 2010 17:40:30 +0100</pubDate>
                        <description><![CDATA[Development of data analysis methods for whole genome sequencing technologies as well as supporting data management and automation within the department of human genetics<span lang="EN-AU"><br />Within the department of human genetics of the RUNMC we are currently working with a new technology for the analysis of the complete human DNA. For the analysis of these huge amounts of sequencing and microarray data as well as the data management and automation we are currently looking for assistance within the current group of enthusiastic bioinformaticians.</span>]]></description>
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                        <title><![CDATA[PhD Researcher on concept recognition and disambiguation in biomedical literature and clinical records ]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/phd-researcher-on-concept-recognition-and-disambiguation-in-biomedical-literature-and-clinical-recor/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/phd-researcher-on-concept-recognition-and-disambiguation-in-biomedical-literature-and-clinical-recor/</guid>
                        <pubDate>Wed, 24 Feb 2010 11:09:11 +0100</pubDate>
                        <description><![CDATA[The PhD researcher will investigate, develop, and evaluate natural language processing techniques for the unambiguous and accurate detection of entities in text, using user feedback to automatically improve detection performance. The main application domain will be genomics with its highly ambiguous nomenclature. <br /> <br /> <b>Project description<br /></b>A lot of scientific knowledge is contained in unstructured text, such as the scientific literature. The first step in extracting this knowledge is identifying the relevant concepts mentioned in the text. Concept recognition in the biomedical domain is extremely difficult due to a wide use of synonyms (several names for the same entity) and homonyms (several entities with the same name). In this project, the PhD student will investigate ways to improve the recognition of concepts by using a wide range of information sources, such as the text around the ambiguous terms, background knowledge about concepts, and background knowledge about the text (e.g. the journal or the author). A key element will be user feedback: users will be able to correct the system, and the system should learn from this feedback.&nbsp;]]></description>
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                        <title><![CDATA[Bioinformatician at the Radboud University Nijmegen Medical Center ]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/bioinformatician/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/bioinformatician/</guid>
                        <pubDate>Fri, 19 Feb 2010 16:18:07 +0100</pubDate>
                        <description><![CDATA[Development of data analysis methods for whole genome sequencing technologies as well as supporting data management and automation within the department of human genetics<br /> <br /> Within the department of human genetics of the RUNMC we are currently working with a new technology for the analysis of the complete human DNA. For the analysis of these huge amounts of sequencing and microarray data as well as the data management and automation we are currently looking for assistance within the current group of enthusiastic bioinformaticians.<br /> ]]></description>
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                        <title><![CDATA[Open positions for Computer Scientists or Bioinformaticians]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/open-positions-for-computer-scientists-or-bioinformaticians/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/open-positions-for-computer-scientists-or-bioinformaticians/</guid>
                        <pubDate>Fri, 19 Feb 2010 11:53:26 +0100</pubDate>
                        <description><![CDATA[Two Ph.D. fellowships are available in the Microbial Genomics and Bioinformatics group of Prof. Glöckner at the MPI-Bremen. The group is focused on the bioinformatics side of modern microbial genomics, phylogeny and data integration, see<link http://www.microbial-genomics.de> www.microbial-genomics.de</link>.
The Ph.D. fellowships are part of a multi-national research projects MAMBA (Marine Metagenomics for new Biotechnological Applications) and MIMAS (Microbial Interactions in MArine Systems) funded by the European Union (<link http://mamba.bangor.ac.uk/>http://mamba.bangor.ac.uk/</link>) and the Federal Ministry of Education and Research (<link http://www.mimas-projekt.de>www.mimas-projekt.de</link>), respectively. The task will be to participate in mining large amounts of next-generation sequencing data from marine habitats, with a focus on ecological functioning as well as enzyme candidates with potential biotechnological applicability.]]></description>
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                        <title><![CDATA[PhD-student and Post-doc position]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/phd-student-and-post-doc-position/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/phd-student-and-post-doc-position/</guid>
                        <pubDate>Fri, 19 Feb 2010 11:22:09 +0100</pubDate>
                        <description><![CDATA[<span lang="EN-GB">The departments of psychiatry and biological psychology of the VU University Medical Center and VU University collaborate in a large-scale study into the genetics of major depressive disorder. </span><span lang="EN-US">For this study, genome-wide data (SNP and CNV) are available. </span><span lang="EN-GB">Recently, further funding was obtained from the National Institutes of Health in America and the Dutch interuniversity ‘Center for Medical Systems Biology (CMSB)’, which will be used to generate gene-expression profiles of normal twins and depressed persons. This will enable us to examine the gene-environment interaction in predicting major depressive disorder. </span>To achieve this, we will use both existing statistical models, but also further develop those to better answer the study’s research questions. For that, we will collaborate with Dr. de Menezes from the Biostatistics group at the VU University Medical Center.]]></description>
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                        <title><![CDATA[Postdoc Bioinformatics – Integration of different types of biological information in genomics analysis]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoc-bioinformatics-integration-of-different-types-of-biological-information-in-genomics-anal/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoc-bioinformatics-integration-of-different-types-of-biological-information-in-genomics-anal/</guid>
                        <pubDate>Tue, 02 Feb 2010 16:19:46 +0100</pubDate>
                        <description><![CDATA[<b><span lang="EN-US">Postdoc Bioinformatics – Integration of different types of biological information in genomics analysis: from pathway back to sequence</span></b><span lang="EN-US"><br />Biological effects are generally the result from interactions between a magnitude of related gene products and metabolites. Studying these cellular components on a high-throughput scale is a main focus of current research in genomics. As such, analysis on the level of biological pathways is very important for the understanding of the outcome of these studies. Recently, the departmentof Bioinformatics has introduced Wikipathways, in collaboration with the University of California, San Francisco. This community based pathway platform supports development and curation of pathways (<link http://www.wikipathways.org>www.wikipathways.org</link>) and has already been used by international domain experts to contribute content. Directly connected to this effort, our department has developed a novel pathway analysis tool, PathVisio (<link http://www.pathvisio.org>www.pathvisio.org</link>). PathVisio is a Java-based, open-source tool.  </span><span lang="EN-US"></span>
<span lang="EN-US">The focus of the postdoc position is on the integration of various types of available biological information by making use of network analysis. A commonly used tool for visualizing, modeling and analyzing molecular and genetic interaction networks is the free software package Cytoscape. Cytoscape is very flexible and allows users to extend its functionality by creating or downloading additional software models called “plugins”. The networks can be analyzed by identifying putative functional and structural modules. A connection between Wikipathways and Cytoscape is already realized, enabling the exchange of information.</span><span lang="EN-US"></span>
<span lang="EN-US">First, all the interactions between gene products and metabolites present in Wikipathways and information available in genomics repositories should be integrated. By integrating these information repositories a complete overview of interactions can be generated. Adding more data does not automatically lead to a better understanding of the mechanism, it can also make the interpration more complex. Therefore, it is necessary to select the most important information. This filtering can be done in several ways.</span><span lang="EN-US"></span>
<span lang="EN-US">Second, additional information on more recently discovered gene and protein regulation mechanisms should be added to the pathways in WikiPathways. Regulation of gene expression and proteins occurs at several levels by for example transcription factors and microRNAs. Various databases describe target sites for these gene regulators. By coupling the information on target sites to the genes present in the pathways, regulation can be incorporated, taking the visualization and analysis of pathways to the next level.</span><span lang="EN-US"></span>
<span lang="EN-US">Third, a single nucleotide polymorphism (SNP), which is a variation of a single nucleotide in a DNA sequence on population level, can be related to a certain disease state or susceptibility to pathogens. Genes within the pathways should be linked to important SNPs. This will enable the analysis of SNP arrays and in the near future sequencing studies. The postdoc will collaborate with excellent researchers in nutrigenomics and nutrigenetics to use the data integration approaches developed in real life studies and will visit some of the research groups involved.</span><span lang="EN-US"></span>
<span lang="EN-US">Bioinformatics is evolving rapidly. One should keep up with novel techniques and methods. This makes Bioinformatics a challenging research field with new and exciting opportunities.</span><b><span lang="EN-US"></span></b> ]]></description>
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                        <title><![CDATA[(senior) software engineer for 'e-Laboratories']]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/senior-software-engineer-for-e-laboratories/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/senior-software-engineer-for-e-laboratories/</guid>
                        <pubDate>Fri, 22 Jan 2010 12:12:23 +0100</pubDate>
                        <description><![CDATA[e-Laboratories are web applications for a specific group of researchers based on  reusable and interoperable components that can be easily deployed by, in this  case, bioinformaticians. In the context of providing e-Science support for the  Dutch bioinformatics support program 'BioAssist', you will be responsible for  building infrastructure and tooling for e-laboratories, and participate in  projects that deploy these. You will be part of a project team of industrial  strength software engineers using professional software engineering practice in  an academic environment. You collaborate with the central engineering team of  BioAssist, the myGrid development team in the UK, and expert users associated  with BioAssist. BioAssist application areas include genomics, proteomics,  biobanking, and systems biology. Your job includes implementation, user support,  and eventually extends to technical project management. The initial contract is  for 2 years. Your main location will be the Human Genetics Department of the  Leiden University Medical Centre, one of the main hubs in the genomics and the  BioBanking community. You will also work 'on location' for the deployment of  specific e-Laboratories or when developing core components with other software  engineers.]]></description>
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                        <title><![CDATA[Postdoc in bioinformatics on genomics/epigenomics (Brussels)]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoctoral-position-at-laboratory-of-cancer-epigenetics/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoctoral-position-at-laboratory-of-cancer-epigenetics/</guid>
                        <pubDate>Fri, 15 Jan 2010 10:05:40 +0100</pubDate>
                        <description><![CDATA[A postdoctoral position is available for a successful candidate to join a dynamic team located in Brussels (Belgium). The group is interested to study genomics and epigenomics in cancer. <br /> <br /> The candidate will tackle integrative analysis of higth-throughput transcriptomics, genomics and epigenomics data sets generated using cutting edge genome-wide technologies. Both clinical and fundamental aspects of cancerogenesis will be addressed.
The position is funded for 2 years, with possible extension. Screening of applications begins immediately and continues until an outstanding candidate is selected.]]></description>
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                        <title><![CDATA[Post-Doc in Computational and Systems Biology ]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/post-doc-in-computational-and-systems-biology/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/post-doc-in-computational-and-systems-biology/</guid>
                        <pubDate>Tue, 12 Jan 2010 17:13:34 +0100</pubDate>
                        <description><![CDATA[The position is funded through the SystemsX.ch DynamiX project <link http://www.systemsx.ch/index.php?id=151 - external-link-new-window "Opens external link in new window">“A Systems Approach to the Yeast Transcriptional Regulatory Network”</link>. The DynamiX project is a collaborative project that involving the Maerkl (EPFL), Shore (U Geneva), Unser (EPFL) and Naef (EPFL) labs.<br /> <br /> The specific project involves studying the transcriptional regulation of ribosome biogenesis in the yeast Saccharomyces cerevisiae and the role of chromatin structure in this process. The Shore and Maerkl labs have generated a large body of data, e.g. ChIP-seq and in vitro binding energy measurements for the major transcription factors involved in ribosome biogenesis, which will be analyzed and modeled in combination with publicly available data such as nucleosome position maps. Specifically, the candidate will apply computational tools to combine these data and construct a computational model of the gene regulation network based on biophysical principles. Computational prediction should suggest new experiments, such as the design of synthetic promoter constructs to be tested directly in fluorescent reporter assays.&nbsp;
<span lang="EN-GB">The successful candidate will develop research  activities pertaining to:</span>
<ul style="margin-top: 0cm;" type="disc"><li class="MsoNormal"><span lang="EN-GB">Analysis of chromatin immunoprecipitation data from  ultra high-throughput sequencing</span><em><span lang="EN-GB"></span></em></li><li class="MsoNormal"><span lang="EN-GB">Integration of public datasets and designing relevant  comparative studies</span></li><li class="MsoNormal"><span lang="EN-GB">Biophysical modelling of transcription regulatory  networks</span></li><li class="MsoNormal"><span lang="EN-GB">Quantification of time-lapse imaging  data</span><em><br /></em></li></ul>]]></description>
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                        <title><![CDATA[Bioinformatician Oncogenomics in a Biotech company]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/bioinformatician-oncogenomics-in-a-biotech-company/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/bioinformatician-oncogenomics-in-a-biotech-company/</guid>
                        <pubDate>Tue, 12 Jan 2010 17:05:01 +0100</pubDate>
                        <description><![CDATA[<span lang="EN-GB">The Bioinformatician shall collaborate with academic parties to evaluate and ensure the implementation of their discoveries in the medical diagnostic market. Key domains for this Bioinformatician are in product feasibility investigations, research and product development. The candidate will closely collaborate internally with another bioinformatician, a bio-statistician, technicians, the quality assurance and regulatory group and consultants dedicated to various topics and externally with Affymetrix Bioinformatics and Chip design.</span>]]></description>
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                        <title><![CDATA[PhD Fellowships in Computational Biology and Scientific Computing]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/phd-fellowships-in-computational-biology-and-scientific-computing/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/phd-fellowships-in-computational-biology-and-scientific-computing/</guid>
                        <pubDate>Fri, 11 Dec 2009 17:19:01 +0100</pubDate>
                        <description><![CDATA[<b>Computational Biology</b>: biological sequence analysis · sequence comparison ·&nbsp; phylogeny reconstruction genome analysis · gene expression and proteomics data analysis · transcriptional regulation · modeling and simulation of biological processes · data integration techniques · mathematical modeling of biochemical reaction networks · systems biology · algorithms and statistical methods for molecular biology. 
<b>Scientific Computing</b>: scientific engineering and industrial modeling · inverse problems · optimization and visualization · algorithm oriented numerical analysis · nonlinear systems · ordinary differential equations partial differential equations · Markov chains · adaptive finite element methods · free boundary problems applications in phase transitions · porous media flow · continuum mechanics · long-term behaviour of nonlinear highly oscillatory dynamical systems · statistical modeling and efficient simulation algorithms modeling and efficient algorithms for fast time scales.]]></description>
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                        <title><![CDATA[Postdoc Bio-informatics]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoc-bio-informatics/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoc-bio-informatics/</guid>
                        <pubDate>Fri, 11 Dec 2009 17:00:13 +0100</pubDate>
                        <description><![CDATA[<span lang="EN-US">We are looking for a postdoctoral fellow bioinformatics/-statistics who will help us to analyze complex metagenomic data in relation to epidemiological parameters. Besides the complex problem of interpreting phylogenetic data of microbiota, we find there are currently no generally accepted statistical methods available to analyze complex communities in relation to epidemiological determinants, especially not in multivariate ways.</span>
<span lang="EN-US">Our final goal is to model complex microbiota with the help of environmental and individual characteristics, with the ultimate goal to predict when disease will develop and to design preventive strategies.</span>]]></description>
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                        <title><![CDATA[Postdoctoral positions available in MIT Computational Biology group]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoctoral-positions-available-in-mit-computational-biology-group/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoctoral-positions-available-in-mit-computational-biology-group/</guid>
                        <pubDate>Fri, 11 Dec 2009 16:41:27 +0100</pubDate>
                        <description><![CDATA[Applicants are sought for the following ongoing projects:
(1) Integrative analysis of genomic and epigenomic datasets in the human genome, in the context of the NIH Epigenome Roadmap and ENCODE projects. Goal is to use many chromatin marks in multiple cell types in order to discover and interpret chromatin states, understand their biological roles, and their dynamics in differentiation and disease (NIH RC1-HG005334, NIH U54-HG004570). 
(2) Integrative analysis of the Drosophila modENCODE project. Goal is to systematically understand the functional elements encoded in the fly genome, and the regulatory logic defining transcription factor binding and chromatin domains, and guiding developmental programs (NIH RC2-HG005639, NIH U54-HG004555). 
(3) Regulatory genomics in human and fly genomes. Goal is to discover regulatory motifs, enhancers, and cis-regulatory modules in the human and fly genomes, and develop predictive models of gene regulation using comparative genomics and large-scale experimental datasets (NIH R01-HG004037). 
(4) Role of non-coding RNAs in chromatin. Goal is to understand the role of small and large non-coding RNAs in directing, establishing, and maintaining chromatin modifications in human embryonic stem cells and during differentiation and cancer (Collaborative work with Ron Hart at Rutgers and John Rinn at HMS). 
(5) Additional projects are available in comparative genomics, genome interpretation, microRNA regulation, phylogenomics, image analysis, RNA structure, and applicants are welcome to define their own projects within the context of ongoing activities in the group (NSF 0644282, NIH U01-HG004264, NSF 0936234).]]></description>
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                        <title><![CDATA[Bio-informatician]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/bio-informatician/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/bio-informatician/</guid>
                        <pubDate>Thu, 26 Nov 2009 09:36:12 +0100</pubDate>
                        <description><![CDATA[The Genomics unit of the Center for Biomics facilitates among others next generation sequencing and microarray analyses. The combination of genome structure, annotation and genome related experimental data in an accessible and comprehensible way is a major challenge. The candidate will be responsible for developing and implementing a browser based tool enabling visualization of the immense data sets and integrated data analysis. This position is part of the BioAssist programme of the Netherlands Bioinformatics Centre (NBIC; <link http://www.nbic.nl/>www.nbic.nl</link>) and in close collaboration with the Bioinformatics Department.]]></description>
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                        <title><![CDATA[2 PhD students for a project at the Plant Systems Biology department ]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/2-pfh-students/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/2-pfh-students/</guid>
                        <pubDate>Mon, 26 Oct 2009 15:09:43 +0100</pubDate>
                        <description><![CDATA[The goal of the Evolutionary Systems Biology lab is to understand how plant developmental systems work and how they evolve. The <i>Arabidopsis</i> root system is in many ways an ideal model system to study developmental processes in plants. Roots have a simple morphology and a relatively small number of cell types, and they exhibit all developmental stages simultaneously. They can be efficiently transformed and chemically perturbed and dure to their near transparency, they offer unmatched opportunities to observe the molecular phenotypes of such treatments. The development of lateral root organs is one of the research foci at the Plant Systems Biology department. We are looking for a PhD student to reverse engineer the lateral root initiation (LRI) process and its interface with hormone signaling and cell cycle processes from molecular and morphological data. We are also looking for a PhD student to study the impact of duplication of functional divergence of developmental regulators on the evolution of LRI and other developmental processes. The project will initially be focused on Aux/IAAs and ARFs, two classes of transcriptional regulators that play important roles in auxin responses and plant development. 			 ]]></description>
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                        <title><![CDATA[Bioinformatics scientist sequence applications]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/bioinformatics-scientist-sequence-applications/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/bioinformatics-scientist-sequence-applications/</guid>
                        <pubDate>Tue, 13 Oct 2009 14:36:41 +0200</pubDate>
                        <description><![CDATA[As a scientist you will be responsible for the analysis and method development for next generation sequencing applications. You will take the scientific lead for sequence analysis in the field of plant breeding application, with the use of novel methods for assembly, mapping and variation detection. You will be responsible for quality control and method implementation. You will work in a team of 5 professional Bioinformaticians and in close collaboration with researchers from other research domains. The team operates under the supervision of a team leader.&nbsp; ]]></description>
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                        <title><![CDATA[Bioinformatics Expert VIB]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/bioinformatics-expert/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/bioinformatics-expert/</guid>
                        <pubDate>Mon, 12 Oct 2009 16:36:13 +0200</pubDate>
                        <description><![CDATA[VIB is looking to expand its Institute-wide bioinformatics platform, BITS (<link http://www.bits.vib.be/>http://www.bits.vib.be</link>), with a bioinformatics expert. Your goal will be to support cutting-edge projects involving high throughput genomics datasets generated by whole-genome sequencing projects using multiple platforms (Illumina, SOLiD, 454, Complete Genomics, others). You will play a key role in setting up a Bioinformatics-infrastructure to enable processing, analysis, visualization and dissemination of genomics datasets, unprecedented in scale. In this position, you will also broker between VIB scientists and leading genomics and bioinformatics companies to discuss study design, sequence analysis strategies and data processing as well as IT-infrastructure. You will assist in the analysis of the generated data and disseminate information through comprehensive research reports and presentations. Additionally, you will evaluate new and existing algorithms, software (commercial and open source) and computer infrastructure requirements. This is a once-in-a-lifetime opportunity to pioneer a bioinformatics platform to enable translational genomics at VIB.]]></description>
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                        <title><![CDATA[Postdoc or PhD Student Computational Biology, visual analysis of Computer Tomography Scans]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoc-or-phd-student-computational-biology-visual-analysis-of-computer-tomography-scans/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoc-or-phd-student-computational-biology-visual-analysis-of-computer-tomography-scans/</guid>
                        <pubDate>Mon, 12 Oct 2009 16:27:50 +0200</pubDate>
                        <description><![CDATA[The research group of Prof. R. van Liere,&nbsp; Centre for Mathematics and Computer Science Amsterdam has a vacancy for a PhD Student or postdoc for the project&nbsp;'A Visual Exploration environment for Analyzing gene Regulation in Developmental processes''.
The project is financed by the Netherlands Organisation for Scientific Research, NWO, <br />research program Visual Interactive Effective Worlds (VIEW). The project is a collaboration with the research group from Dr. J.A. Kaandorp (Section Computational Science, University of Amsterdam). In this project we propose to develop visualization techniques for quantitative research on complex shaped and variable biological and simulated objects and techniques for the visualization of abstract n-dimensional parameter spaces in models of gene regulatory networks. The project aims to develop methods and tools to extract and present geometrical information from spatial measurements and simulation, to develop visualization methods to compare simulation models and measured data, and techniques for the navigation of morphometric parameter spaces (morphospaces) and model parameter spaces.&nbsp;In this part of <br />the project we will focus on the analysis of calcification in&nbsp; 3D images (Computer Tomography Scans) of scleractinian corals. A better understanding of calcification in corals is of fundamental importance in research on the potentially detrimental impact of increasing atmospheric carbon dioxide concentrations, reducing ocean pH and carbonate ion concentrations on the calcification process in corals.&nbsp; The candidate is expected to collaborate extensively with&nbsp; biologists.]]></description>
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                        <title><![CDATA[PhD student in Computational Biology for the project: 'Genetic and Cellular Mechanisms for Controlled Growth']]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/phd-student-in-computational-biology-for-the-projectgenetic-and-cellular-mechanisms-for-controlled/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/phd-student-in-computational-biology-for-the-projectgenetic-and-cellular-mechanisms-for-controlled/</guid>
                        <pubDate>Mon, 12 Oct 2009 15:57:20 +0200</pubDate>
                        <description><![CDATA[The Section computational Science (University of Amsterdam) has a vacancy for a PhD Student for the project 'Genetic and Cellular Mechanisms for Controlled Growth' (38 hours per week).
The project is funded by the Honda Research Institute Europe. In this project the candidate will collaborate with researchers from the Honda Research Institute Europe and should be willing to spend 1-2 months each year at this institute in Offenbach (Germany). The candidate is expected to collaborate extensively with molecular developmental biologists.
The main target of the project is to develop computational models for cellular development to achieve a controlled growth. By controlled growth, we mean three mutually related properties. First, the morphological growth should stop within a limited time. This does not necessarily mean that cells should stop dividing, rather, a balance between cell proliferation and cell death should be achieved. Second, it should achieve a desired shape with a sufficient complexity. Third, it should show a certain capability of self-repairing, i.e., when a small number of the cells are destroyed, the balanced cell growth process should be able to re-generate these cells at the right place. Cellular interaction mechanisms that facilitate a structured growth will be studied. Second, evidence indicating mechanisms for controlled growth found in biology, such as the role of negative and positive feedback loops in gene regulatory networks, will be evaluated and related to those network motifs found in the computational model. Based on the understanding of the structure, dynamics and cellular behaviour of the gene regulatory network model, we will perform a case study of a GRN model for the development of cnidarians Nematostella vectensis and Acropora millepora using biological data, including spatio-temporal gene expression data (in situ hybridisations) and morphological data.]]></description>
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                        <title><![CDATA[Postdoc or PhD student in Computational Biology ]]></title>
                        <link>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoc-or-phd-student-in-computational-biology/</link>
                        <guid>http://nbic.roquin.net/about-nbic/jobspositions/detail/jobdetails/postdoc-or-phd-student-in-computational-biology/</guid>
                        <pubDate>Mon, 12 Oct 2009 15:42:11 +0200</pubDate>
                        <description><![CDATA[The Section computational Science (University of Amsterdam) has an open position for the following project: Multi-scale modelling of calcification in scleractinian corals (38 hours per week).
This project is financed by the Netherlands Organisation for Scientific Research (NWO) as part of its Computational Life Sciences research programme. The project is a collaboration with the research groups headed by Prof. R.P.M. Bak (Netherlands Institute for Sea Research (NIOZ) and Prof. D.J. Miller (James Cook University, Australia). The appointee will collaborate extensively with molecular developmental biologists. The central research aim of this project is to characterize the genes that control the&nbsp;differences in coral morphology for related coral species. We will do this by making a quantitative comparison of gene expression patterns, with a special focus on genes that are involved in the process of calcification. To test the hypothesis that these genes can explain the differences in morphology, we plan to use the estimated quantities in a simulated network controlling calcification. We intend to study the emergence of the micro-morphology structure and link gene expression patterns to the corallite structure. This polyp (corallite) based model will be coupled with a macroscopic growth form model describing Ca2+ and HCO3- fluxes from the environment. A better understanding of calcification in corals is of fundamental importance in research on the potentially detrimental impact of increasing atmospheric carbon dioxide concentrations, decreasing ocean pH and carbonate ion concentrations on the calcification process in corals and other calcifying organisms.
The appointee will work on multi-scale modelling of calcification in scleractinian corals using computational approaches.]]></description>
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