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Interdisciplinary Centre for Bioinformatics (IZBI)

Research Activities at the Centre

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Research Activities at the Centre

General

The DFG-funded Bioinformatics Initiative Leipzig pursues an interdisciplinary approach bringing together experimental bioscientists (i.e. cell biologists, biochemists, pathologists, clinicians involved in basic research) and experts trained in the analysis of complex data and formal modelling of structures and processes (i.e. computer scientists, biostatisticians, biomathematicians). The particular local research profile and the request for bioinformatics support led us to select two major fields of research.

(1) In Genetic Evolution we pursue projects to analyse genetic diversity and to use this knowledge to identify evolutionary relationships among species (i.e. phylogeny reconstruction), compare humans and chimpanzees, and obtain an understanding of the complexities of biological processes (e.g. the evolution of genetic regulation).

(2) In Tissue Formation and Cellular Signal Transduction we concentrate on understanding genotype and phenotype dependency in tissue formation and function. Several projects are planned to elucidate the mechanisms of the spatial formation of tissues (e.g. epithelia, tumours, engineered tissues), to investigate the architecture of signal transduction and genetic regulatory networks, and to analyse high-dimensional genomic and molecular data from manipulated normal and diseased tissues (e.g. gene expression analysis).

Regarding the teaching of bioinformatics, the objective of the DFG Bioinformatics Initiative Leipzig is to build up a curriculum for about 30 students annually.

In 2002 the DFG Bioinformatics Initiative Leipzig achieved the following:

(1) An interacting network of local partners was established which contributes to the teaching, research and functioning of our infrastructures. It involves scientists from five faculties of Universität Leipzig, the Max Planck Institutes of Evolutionary Anthropology (MPI EVA) and Mathematics in the Natural Sciences (MPI MIS), and new centres such as the BBZ Biotechnology-Biomedicine Centre, the Interdisciplinary Centre for Clinical Research (IZKF) and the Clinical Trials Coordinating Centre (KKSL, both funded by the German Ministry of Education and Research).

(2) The Interdisciplinary Centre for Bioinformatics (IZBI) was established as a key infrastructural element. Consequently, it has its own staff, premises and administration. It became fully functional by the end of 2002. IZBI employs core research staff, one junior research group, temporary personnel for project groups, and doctoral students. IZBI assists its partners on selected joint R&D projects. Service projects (e.g. for data analyses or database developments) are handled on a consultancy or contract basis. The first projects have reached publication status and the first grants are in preparation.

(3) A C4 professorship in Bioinformatics was established as a second important infrastructural unit. Prof Peter Stadler joined the faculty of Mathematics and Computer Science in September 2002. His group is now operative.

Research concept

IZBI offers its partners a novel approach to research management in order to meet their demands as efficiently as possible.

Projects: IZBI is designed to support cooperating scientists on a project basis. Projects can be either research projects (with a scientific aim) or service projects (designed to develop a technology or routine data analysis). A project is headed by a principal investigator. For each project we request a project proposal detailing the objective, work plan, project team (including the responsibilities of IZBI's staff and the personnel from the participating partners) and budget plan (IZBI resources required, other resources, grants). Depending on the complexity of the task IZBI can support the project with resources ranging from short-term student employment or a temporary task force to a full scale team involving several experts for many months. The scientific coordinators discuss the quality, feasibility and compatibility of the project proposals with the principal investigators. The proposals are evaluated by the board of directors and external reviewers. Scientific quality, consistency with the research profile and financial feasibility are the key criteria for deciding whether to support a project.
Any researcher from the university (including the IZBI members themselves) and the supporting MPIs can submit a project proposal at any time. The projects selected are supported whenever possible with IZBI funds.

Working groups: To establish an interactive interface with partners and to bring together the expertise at IZBI, it was decided to organise the personnel into working groups. Working groups consist of IZBI research staff members and scientists from the participating institutes. They have regular meetings, discuss research results, invite guests, discuss new project proposals, and conduct courses and seminars. Scientific coordinators stimulate and coordinate these activities and supervise the progress of projects and of skills. Four working groups have been implemented:

Working Group 1 (Data Base and Data Integration; coordinator Prof Rahm) focuses particularly on design projects for data warehouses for genomic and molecular data and related annotations. Being a methodological working group, it works together with all the other working groups. It was set up in autumn 2001 and has two core staff members.

Working Group 2 (Tissue Organisation; coordinator Dr Drasdo) focuses on understanding spatial tissue formation. It pursues projects using simulation models and the 3D image reconstruction of microscopy data. Two specialists were employed in 2002 as core staff researchers.

Working Group 3 (Signal Transduction and Gene Expression; coordinator Prof Horn) was set up in summer 2002. It addresses gene expression analysis and cellular signal transduction. A junior research group is associated with WG3:

Junior Research Group (Complex Regulatory Networks; PD Dr Bornholdt) This group studies the dynamics and function of complex regulatory network systems. Examples range from the molecular level of gene regulation and signal transduction networks to cellular systems such as the immune system and the brain. The group's goal is to develop methods, models and strategies for studying the dynamics of complex regulatory network systems.

Working Group 4 (Genetic Evolution; coordinator since September 2002 Prof Stadler) began its first projects in autumn 2002.

Research projects

Databases and Data Integration (WG1)

Project: Data warehouse design and implementation to support gene expression analysis
Rahm, Do, Kirsten

Tissue Organisation (WG2)

Project 1: 3D characterisation of the invasion front of human cervical carcinoma
Einenkel, Braumann, Kuska, Horn, Drasdo, Höckel

Project 2: 3D morphological analysis of vascular structures in artificial tissues
Kuska, Frerich

Project 3: Generic single-cell based model of interacting cells to describe spatial epithelial tissue formation
Drasdo, Galle, Löffler

Project 4: Spatial dynamics of growing tumour spheroids
Drasdo, Höhme

Gene expression and cellular signal transduction (WG3)

This working group dedicated its efforts to a key project on gene expression (GE), providing a service and research platform for future projects. A second project was devoted to signal transduction modelling.

Project 1: Platform for gene expression analysis
Horn, Boriss, Binder, Hasenclever, Kropf, Krohn, Läuter, Löffler, Paschke, Wagner

Project 2: Optimising strategies for the identification of transcriptional networks in haemopoietic progenitor cells
Drasdo , Cross, Missal, Löffler

Junior Research Group: Complex Regulatory Networks
Dr Bornholdt

Genetic Evolution (WG4)

Project: Estimates of recombination from human polymorphism data
Ptak, Przeworski

In addition, two pilot-study projects on functional nucleic acid structures in two distinct virus groups have just been approved by the IZBI board: "Translation from polycistronic mRNAs: RNA secondary structure analysis to identify conserved structural elements" and "Analysis of secondary RNA structure of infectious bursal disease virus (IBDV) genome segment B" (Mueller, Stadler, Johne, Raue).

 

 

 

Home Zusammenstellung: Forschungskontaktstelle, 05.07.2004