Your tasks
- Analyze tRNA modification levels in matched leukemia patient samples collected at diagnosis and relapse, and compare them to healthy hematopoietic specimens using nanopore-based direct tRNA sequencing. Complementary transcriptomic, proteomic, and metabolomic profiling will be performed on the same samples
- Integrate multi-omics data (e.g., using MOFA) to investigate how patient-specific tRNA modification patterns correlate with treatment response and survival
- Functionally validate candidate RNA modifications and their associated enzymes using CRISPR-Cas9 knockouts in both primary healthy and malignant cells, as well as established cell culture models
- Conduct colony-forming unit (CFU) assays, drug synergy screens, ribosome profiling (Ribo-Seq), and nanopore sequencing of modified primary cells and cell lines
- Work in close collaboration with a PhD student from the Frye Lab, particularly on in vivo models and single-cell RNA sequencing (scRNA-seq). Additional collaboration with other research groups within CRC/SFB 1709 is expected
Your profile
- Master degree (or similar) in molecular biology, biomedicine, biotechnology, bioinformatics or a related field
- Experience in molecular biology methods (e.g. PCR, NGS, cell culture) and/or functional cell assays
- Strong interest in cancer biology, RNA biology, and stem cell research
- Bioinformatics experience, e.g. R, preferred
- High motivation, curiosity, and the ability to work independently and in a team as well as good communication skills in english (written and spoken) are expected
Your tasks
- Analyze tRNA modification levels in matched leukemia patient samples collected at diagnosis and relapse, and compare them to healthy hematopoietic specimens using nanopore-based direct tRNA sequencing. Complementary transcriptomic, proteomic, and metabolomic profiling will be performed on the same samples
- Integrate multi-omics data (e.g., using MOFA) to investigate how patient-specific tRNA modification patterns correlate with treatment response and survival
- Functionally validate candidate RNA modifications and their associated enzymes using CRISPR-Cas9 knockouts in both primary healthy and malignant cells, as well as established cell culture models
- Conduct colony-forming unit (CFU) assays, drug synergy screens, ribosome profiling (Ribo-Seq), and nanopore sequencing of modified primary cells and cell lines
- Work in close collaboration with a PhD student from the Frye Lab, particularly on in vivo models and single-cell RNA sequencing (scRNA-seq). Additional collaboration with other research groups within CRC/SFB 1709 is expected
Your tasks
- Analyze tRNA modification levels in matched leukemia patient samples collected at diagnosis and relapse, and compare them to healthy hematopoietic specimens using nanopore-based direct tRNA sequencing. Complementary transcriptomic, proteomic, and metabolomic profiling will be performed on the same samples
- Integrate multi-omics data (e.g., using MOFA) to investigate how patient-specific tRNA modification patterns correlate with treatment response and survival
- Functionally validate candidate RNA modifications and their associated enzymes using CRISPR-Cas9 knockouts in both primary healthy and malignant cells, as well as established cell culture models
- Conduct colony-forming unit (CFU) assays, drug synergy screens, ribosome profiling (Ribo-Seq), and nanopore sequencing of modified primary cells and cell lines
- Work in close collaboration with a PhD student from the Frye Lab, particularly on in vivo models and single-cell RNA sequencing (scRNA-seq). Additional collaboration with other research groups within CRC/SFB 1709 is expected
- Analyze tRNA modification levels in matched leukemia patient samples collected at diagnosis and relapse, and compare them to healthy hematopoietic specimens using nanopore-based direct tRNA sequencing. Complementary transcriptomic, proteomic, and metabolomic profiling will be performed on the same samples
- Integrate multi-omics data (e.g., using MOFA) to investigate how patient-specific tRNA modification patterns correlate with treatment response and survival
- Functionally validate candidate RNA modifications and their associated enzymes using CRISPR-Cas9 knockouts in both primary healthy and malignant cells, as well as established cell culture models
- Conduct colony-forming unit (CFU) assays, drug synergy screens, ribosome profiling (Ribo-Seq), and nanopore sequencing of modified primary cells and cell lines
- Work in close collaboration with a PhD student from the Frye Lab, particularly on in vivo models and single-cell RNA sequencing (scRNA-seq). Additional collaboration with other research groups within CRC/SFB 1709 is expected
Your profile
- Master degree (or similar) in molecular biology, biomedicine, biotechnology, bioinformatics or a related field
- Experience in molecular biology methods (e.g. PCR, NGS, cell culture) and/or functional cell assays
- Strong interest in cancer biology, RNA biology, and stem cell research
- Bioinformatics experience, e.g. R, preferred
- High motivation, curiosity, and the ability to work independently and in a team as well as good communication skills in english (written and spoken) are expected
- Master degree (or similar) in molecular biology, biomedicine, biotechnology, bioinformatics or a related field
- Experience in molecular biology methods (e.g. PCR, NGS, cell culture) and/or functional cell assays
- Strong interest in cancer biology, RNA biology, and stem cell research
- Bioinformatics experience, e.g. R, preferred
- High motivation, curiosity, and the ability to work independently and in a team as well as good communication skills in english (written and spoken) are expected
We offer
- Goal-oriented, individual training and development opportunities
- Working with the latest techniques / technical equipment
- Possibility of doctorate
- Possibility to publish scientifically is offered and supported
- Regular team meetings
- Close collaboration within SFB/CRC1709
- Collectively agreed remuneration, 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
We offer
- Goal-oriented, individual training and development opportunities
- Working with the latest techniques / technical equipment
- Possibility of doctorate
- Possibility to publish scientifically is offered and supported
- Regular team meetings
- Close collaboration within SFB/CRC1709
- Collectively agreed remuneration, 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
- Goal-oriented, individual training and development opportunities
- Working with the latest techniques / technical equipment
- Possibility of doctorate
- Possibility to publish scientifically is offered and supported
- Regular team meetings
- Close collaboration within SFB/CRC1709
- Collectively agreed remuneration, 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
Contact & Application
For further information please contact Cornelius Pauli via e-mail.
Interested?
Applications will be accepted until 10.08.2025 direct online.
Klinik für Hämatologie, Onkologie und Rheumatologie
Dr. Cornelius Pauli
Im Neuenheimer Feld 410
69120 Heidelberg
Tel.: 06221-56-32254
MoritzCornelius.Pauli@med.uni-heidelberg.de
For further information please contact Cornelius Pauli via e-mail.
Interested?
Applications will be accepted until 10.08.2025 direct online.
Klinik für Hämatologie, Onkologie und Rheumatologie
Dr. Cornelius Pauli
Im Neuenheimer Feld 410
69120 Heidelberg
Tel.: 06221-56-32254
MoritzCornelius.Pauli@med.uni-heidelberg.de