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Your position The goal of the project is to understand the cause of multiple sclerosis, focusing on the interactions between autoreactive B cells, the lymphotropic virus EBV, and the cellular
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analysis, and next-generation sequencing (NGS) of pooled CRISPR libraries, offering the opportunity to combine rigorous in vivo experimentation with systems-level approaches. Your main tasks will be: A
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, and next-generation sequencing (NGS) of pooled CRISPR libraries, providing a unique opportunity to combine rigorous in vivo experimentation with systems-level approaches. Your main tasks will be: A
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integrate large language models, multilingual AI, and confidential HPC to support patients and clinicians in real-world healthcare environments. You will lead research on trustworthy and aligned LLMs
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expression studies (“bulk" and single-cell RNA-seq) and gene regulation studies (ChIP-seq, ATAC-seq, DNA variants calling), long reads sequencing, proteomics and spatial transcriptomics Set up robust and
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-on mouse experience will not be considered. The project also includes high-throughput metabolic profiling of genetic perturbations, computational data analysis, and next-generation sequencing (NGS) of pooled
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for the CADENCE Core Facility . This position plays a central role as the interface between the Department and the Core Facility, ensuring seamless coordination, strategic alignment, and high‑quality
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role of drug transporters and drug-metabolizing enzymes in these processes. Both transporters and enzymes are influenced by multiple factors, including naturally occurring genetic variants, which
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of neuroimmunological diseases, with a particular focus on multiple sclerosis and MOG-antibody associated disease (MOGAD). We study how immune cells including B cells and gut microbiome contribute to the initiation and
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, and scalability Collaborating closely with psychologists, physiologists, and other heat domain experts to ensure that models align with theoretical constructs and applications Leading and co-authoring