More information

Ingo Roeder Group

Systems biology with applications in medicine, (stem) cell and developmental biology

Our group develops and applies mathematical models and simulation strategies of regulatory processes on the molecular, the cellular, and the tissue level with the aim to understand and potentially predict the behavior of biological systems. Major foci are medically relevant topics, such as the investigation of principles of stem cell organisation ("theoretical stem cell biology") and of mechanisms of cancer development and treatment. Further research topics are statistical/computational methods to study complex experimental data (e.g. cellular genealogies) and image analysis procedures (e.g. model-based segmentation algorithms in the context of automatic single cell tracking).

Specific projects in the field of Medical Systems Biology / Mathematical Modelling include the investigation of stem cell - niche (i.e. local growth environment) interactions, the analysis and the prediction of clonal competition processes, as well as the modelling of aging-related phenomena in the haematopoietic system. Using agent-based modelling and simulation approaches, we contribute to a better understanding of disease development and/or treatment effects (e.g. the context of leukaemia treatment or gene therapy approaches). Another research field is the understanding of gene regulatory principles on the level of small-scale transcription factor networks. In particular, we are interested in the role of transcription factor interactions for the regulation of pluripotentcy in embryonic (ES) and induced pluripotent stem (iPS) cells.

With respect to the newly emerging field of Bioimage Informatics, our group is specifically interested in the development of automatic single cell tracking algorithms and their application. For the tracking, we apply different types of model-based segmentation methods. The analysis of the resulting single cell data (e.g. cellular genealogy structures complemented with information on cell-cell contacts or cell migration) is done by statistical models, such as generalised linear mixed-effect models or by dynamical networks based on (cell) community structures.

Ingo Röder Research: movie Movie: Automatically tracked haematopoietic stem and progenitor cells on a biomimetic polymer scaffold showing the migratory paths of individual cells over time. Different cell clones are identified by color code. On the right hand side, the corresponding cellular genealogies (same color code), characterising the parental history of individual clones, are shown (see Scherf et al. (2012), Exp. Hematol. 40: 119-130.e9)

Future Projects and Goals

Beside the continuation of the research activities described above, future activities are planned in the following areas:

  • Explicit modelling of biomechanical properties of stem cells (e.g. ES and iPS cells)
  • Modelling proliferation and differentiation of neural stem cells (NSCs)
  • Disease and treatment models of Acute Myeloid Leukaemia (AML)
  • Single cell tracking and modelling of patterning phenomena in early development (e.g. in zebrafish embryos)

Methodological and Technical Expertise

  • Mathematical modelling and computer simulation technices, including differential equation and agent-based models
  • Biostatistics and biometry, including e.g. generalized non-/linear (mixed effect) models
  • Image segmentation and cell tracking methods
  • Theoretical stem cell biology


since 2010
Professor for Medical Statistics and Biometry and Head of the Institute for Medical Informatics and Biometry (IMB), Medical Faculty Carl Gustav Carus, TU Dresden

Habilitation and Venia legendi in “Medical Bioinformatics, Statistics and Epidemiology”

Group leader “Dynamical modelling of stem cell organization”, IMISE, Leipzig

PhD in Theoretical Biology, University Leipzig

Diploma in Mathematics, TU Dresden

More Information

Selected Publications

Schmid B, Shah G, Scherf N, Weber M, Thierbach K, Campos CP, Roeder I, Aanstad P, Huisken J.
High-speed panoramic light-sheet microscopy reveals global endodermal cell dynamics.
Nat Commun. 2013 Jul 24;4:2207. doi: 10.1038/ncomms3207 (2013)

Scherf N, Franke K, Glauche I, Kurth I, Bornhäuser M, Werner C, Pompe T, Roeder I
On the symmetry of siblings: automated single-cell tracking to quantify the behavior of hematopoietic stem cells in a biomimetic setup.
Experimental hematology 40: 119–130.e9 (2012)

Glauche I, Herberg M, Roeder I
Nanog variability and pluripotency regulation of embryonic stem cells – insights from a mathematical model analysis.
PLoS one 5: e11238

Roeder I, Horn K, Sieburg HB, Cho R, Muller-Sieburg C, Loeffler M
Characterization and quantification of clonal heterogeneity among hematopoietic stem cells: a model-based approach.
Blood 112: 4874–83 (2008)

Roeder I, Horn M, Glauche I, Hochhaus A, Mueller MC, Loeffler M
Dynamic modeling of imatinib-treated chronic myeloid leukemia: functional insights and clinical implications.
Nature Medicine 12: 1181–4 (2006)


Medical Faculty Carl Gustav Carus
Dresden University of Technology
Fetscherstraße 74
D-01307 Dresden