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—including next-generation sequencing, single-cell approaches, genome engineering, and spatial biology—to study mechanisms of tumor initiation and progression. Collaborate across disciplines to translate basic
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including mitochondria and lysosomes, and high-throughput proteome profiling of perturbations in iPSC-derived brain cell types. The project will entail a combination of unbiased discovery and hypothesis
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antigens, T cell receptor (TCR) and antigen interactions and their crucial role in anti-cancer immune responses. You'll leverage your strong background in computational biology, machine learning, and
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field; or a Ph.D. in (Molecular) Biology or Immunology with in-depth experience in high-throughput data analysis evidenced by publications. ● You have experience with single-cell and multi-omic data