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) quantification tools, holding back early immunogenicity risk assessment in the context of protein drug development. A clearer understanding of the rules governing T cell activation would form a paradigm shift in
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paradigm shift in development of Biologics. A critical challenge preventing this is the current limiting volume of high quality and well-characterized in-vitro T cell immunogenicity data. In this project, we
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linear ballistic accumulator models, diffusion models, biased competition models, or Bayesian models. During the employment, the candidate is expected to engage in the development of computational models
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