Computational and Single-Cell Epigenomics

Dr. Michael Scherer
Group Leader Computational and Single-Cell Epigenomics
We work on computational solutions for investigating alterations in the epigenomic pattern related to cancer, with a special focus on chances to the DNA methylation pattern. Additionally, we leverage single-cell DNA methylation technologies to investigate methylation changes in rare cell populations.

People
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Dr. Michael Scherer
Group Leader Computational and Single-Cell Epigenomics
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Belen Otero Carrasco
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Sergio Manzano Sanchez
Technician
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Maxime de Vrieze
Running Projects

We investigate whether enhancer hijacking is an understudied and overlooked mechanism of oncogene activation in lung cancer.

Using a combination of bulk assays and single-cell profiling, we are investigating whether epigenetic heterogeneity is associated with leukemogenesis and therapy resistance
Open Projects
We are continuously looking for new people to join our team. At the moment, we have the following open positions:
Bachelor/Master thesis projects in Computational and Single-Cell Epigenomics
We offer a variety of projects ranging from computational tool development, over data analysis, until projects involving wet-lab work. At the moment, we offer the following projects:
- Data analysis tasks around various cancer types using of the RnBeads (rnbeads.org/) toolsuite
- Development of a software tool for the analysis of scTAM-seq data
- Characterizing epigenome heterogeneity in lung cancer
- Predicting chromothripsis from DNA methylation data
Being embedded in the Division of Cancer Epigenomics, we offer a welcoming work atmosphere with a mix of computational and experimental students.
What we are looking for: We are looking for students that are pursuing their Bachelor's and Master's degree at Heidelberg University and that want to do their Bachelor/Master thesis or lab rotation in Computational Epigenomics. Previous experience with programming in R and with epigenomics are advantages.
Publications
- Scherer M, Singh I, Braun M, Szu-Tu C, et al. Clonal tracing with somatic epimutations reveals dynamics of blood ageing. Nature 2025. https://doi.org/10.1038/s41586-025-09041-8
- Bianchi, A., Scherer, M., Zaurin, R., Quililan, K., Velten, L., & Beekman, R. (2022). scTAM-seq enables targeted high-confidence analysis of DNA methylation in single cells. Genome Biology, 23(1), 229. https://doi.org/10.1186/s13059-022-02796-7
- Scherer, M., Nebel, A., Franke, A., Walter, J., Lengauer, T., Bock, C., Müller, F., & List, M. (2020). Quantitative comparison of within-sample heterogeneity scores for DNA methylation data. Nucleic Acids Research, 48(8), e46–e46. https://doi.org/10.1093/nar/gkaa120
- Müller, F., Scherer, M., Assenov, Y., Lutsik, P., Walter, J., Lengauer, T., & Bock, C. (2019). RnBeads 2.0: comprehensive analysis of DNA methylation data. Genome Biology, 20(1), 55. https://doi.org/10.1186/s13059-019-1664-9
- Scherer, M., Nazarov, P. V., Toth, R., Sahay, S., Kaoma, T., Maurer, V., Vedeneev, N., Plass, C., Lengauer, T., Walter, J., & Lutsik, P. (2020). Reference-free deconvolution, visualization and interpretation of complex DNA methylation data using DecompPipeline, MeDeCom and FactorViz. Nature Protocols, 15(10), 3240–3263. https://doi.org/10.1038/s41596-020-0369-6
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