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UKSH Kiel invites a doctoral researcher to join the Bioinformatics & AML group in Kiel. The project aims to discover molecular AML subtypes using bulk and single-cell data, with collaboration across molecular genetics and clinical research.
You will develop reproducible analyses and contribute to open-source tools. The role offers a 3-year appointment under TV-L E13 at 65% effort, with the possibility to pursue a PhD within a dynamic research team and access to high-performance computing
Department of Internal Medicine II, Research Group: Functional Genomics of Acute Leukemia (Heads: Dr. Lorenz Bastian / Prof. Dr. Claudia Baldus)
The position is part of the newly established research project “LUCID-AML – Learning-based Unsupervised Clustering of transcriptomIcs to Detect developmental, functional and prognostic subtypes in AML across age”, funded by the Deutsche José Carreras Leukämie-Stiftung. It is closely linked to our DFG-funded Clinical Research Unit “CATCH-ALL: Towards a Cure for Adults and Children with Acute Lymphoblastic Leukemia”, where clinical and basic researchers work together to define mechanisms of leukemogenesis and treatment resistance across age groups.
Acute myeloid leukemia (AML) affects people of all ages, but its incidence increases steeply in older adults, while survival decreases sharply with age. AML can be classified into transcriptomic groups that reflect cytogenetic lesions, reveal developmental origins and link leukemias to normal hematopoietic states. However, consistent subtype definitions and robustly validated tools for applying them across cohorts are lacking.
The project builds on ALLCatchR and our work on machine-learning frameworks for disease classification and the identification of novel molecular subtypes in acute lymphoblastic leukemia. LUCID-AML will integrate more than 8,000 bulk AML gene-expression profiles from multiple cohorts with single-cell data, molecular genetics, diagnostic classifications, drug-response data and clinical outcomes. The project aims to establish reproducible, gene-expression-based AML subtypes while accounting for age and treatment. Further aims are to define their developmental origins and make the resulting models available as transparent, open-source tools for research and clinical diagnostics. For further reading: Beder et al., HemaSphere, 2023; Bastian et al., Blood, 2024; Beder et al., bioRxiv / HemaSphere, 2026.
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The initial appointment is for three years, with the possibility of extension.
28. October 2026, indicating the reference number 29315.