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We are looking for an enthusiastic Postdoc/PhD to join our research group to study gene regulation in neurodevelopment with a focus on how NR2F1 dosage shapes the specification of neuronal lineages and the formation of cortical circuits.
NR2F1 is a key transcription factor controlling embryonic neuronal development. Mutations and deletions of NR2F1 lead to Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS). Using neuronal cells derived from CRISPR/Cas9 engineered human induced pluripotent stem cells (hiPSC) we model distinct NR2F1 dosages to study their effects across neuronal differentiation. By integrating time-resolved bulk (RNA-seq, ATAC-seq, ChIP-seq, Hi-C) obtained from neuronal lineages cultured in 2D cells and single-cell multi-omics (scRNA-seq, scATAC-seq, Multiome) data generated in 3D forebrain dorsal organoids, we aim to map regulatory networks sensitive to NR2F1 expression levels.
Our group studies the fundamental principles of embryonic neuronal development by combining genomics, gene editing, and bioinformatics. We offer an international, dynamic, and supportive research environment that fosters creativity and career growth. The AG Laugsch is embedded within Heidelberg’s excellent computational biology network, fostering close collaborations with experts like Carl Herrmann (Institute of Pharmacy and Molecular Biotechnology), and Julio Saez-Rodriguez (Systems Biomedicine, Institute of Computational Biomedicine. If you are a curiosity-driven researcher who enjoys interdisciplinary teamwork and tackling complex biological questions through data, we would be delighted to hear from you. The application must include your motivation, a brief statement of your scientific interests, contact details from three references, curriculum vitae, separated publication list, and relevant certificates.
https://www.klinikum.uni-heidelberg.de/humangenetik/forschung/ag-laugsch/
Literature:
https://doi.org/10.64898/2026.06.25.734423
https://doi.org/10.64898/2026.05.01.722223
doi: 10.1016/j.stem.2019.03.004.
- Job-ID: V000015909
- Einsatzgebiet: Institut für Humangenetik
- Einsatzort: Heidelberg
- Tätigkeitsbereich: Wissenschaft und Lehre
- Anstellungsart: Vollzeit
- Veröffentlicht: 13.07.2026
- Befristung:Befristet (3 Jahre)
- Vertrag:TV-L
Ihre Aufgaben
- Establish computational pipelines for the analysis and integration of single-cell multi-omics data (scRNA-seq, scATAC-seq, Multiome) to reconstruct gene regulatory networks in 3D forebrain dorsal organoids to determine pathophysiological consequences of aberrant NR2F1 dosage
- Design and build an interactive, open-access web platform for visualization and usage of multi-omics datasets
- Integrate newly generated data with in-house and publicly available datasets to interpret results in a robust biological context
- Ensure reproducibility, data management, and documentation of computational workflows in high-performance computing environments
- Collaborate closely with experts in computational biology across the university and affiliated institutes, as well as with experimental researchers (wet lab) in the AG Laugsch, to support accurate data interpretation and integration
- Maintain clear documentation of analyses and computational workflows on eLab and provide regular progress reports and updates
- Actively participate in regular journal clubs and institute meetings. Present findings at lab meetings and international conferences and contribute to manuscripts and grant applications.
Your Profile
- Strong background in bioinformatics or computational biology
- Practical experience with omics data pre-processing, pipeline development, and high-performance computing
- Proficiency in R or Python, and shell scripting
- Interest in gene regulation and developmental biology
- Optional previous experience with epigenomic data analysis or gene regulatory network inference
- Ability to work independently and collaboratively in a multidisciplinary environment
- Excellent written and spoken English skills
What we offer
- Collectively agreed remuneration TV-L E13, attractive company pension scheme (VBL)
- 30 days vacation
- Sustainable travel: job ticket
- Family-friendly working environment: cooperative arrangements for childcare, subsidy for child vacation care, advice for employees with relatives in need of care
- Wide range of health, prevention and sports offers
- Possibility to publish scientifically is offered and supported
- Regular team meetings
- Possibility of doctorate
Kontakt & Bewerbung
For further information please contact Dr. rer. nat. Magdalena Laugsch via e-mail.
Interested?
Applications will be accepted until 31.08.2026 online.
Institut für Humangenetik
Dr. rer. nat. Magdalena Laugsch, Group Leader
Im Neuenheimer Feld 366
69120 Heidelberg
+49 6221 56-39128
Magdalena.Laugsch@uni-heidelberg.de
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