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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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models, multi-omics analyses (e.g., RNA-seq, ATAC-seq, scRNA-seq, scDNA-seq, WES/WGS, targeted NGS, DigiWest), a broad spectrum of molecular and cellular biology techniques, biochemistry and biophysics
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machine learning for transport simulation. A core innovation involves Bayesian metamodeling techniques to construct fast surrogate models of the simulation space, enabling efficient scenario analysis
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use computational approaches to mine natural biodiversity in gene sequences to identify engineering targets to increase lipid content and enhance the water use efficiency. The project will make use
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target groups respond to science. This is the first large-scale study of its kind, and your results will establish a legacy of scientists working with funding councils to defend their research. Cutting
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questionnaires and interview questions, conduct interview with target participants etc.), analyze research data, draft research reports and other resources, assist in publication of research papers, liaise with
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) Number of Vacancies 3 Target Hire Date Expected End Date Contact Information for Candidates Prof. Mohammed Hassan, Assistant Professor of Physics and Optical Sciences mohammedhassan@arizona.edu Open Date 7
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Postdoctoral Research Associate - Basic and Translational Research Training in Pediatric Classical H
by training in the execution of statistically rigorous, hypothesis-driven research that probes the mechanistic basis of hematologic disease, uncovers new therapeutic targets, and translates
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propagation problems, stochastic partial differential equations, geometric numerical integration, optimization, biomathematics, biostatistics, spatial modeling, Bayesian inference, high-dimensional data, large
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expertise in bioinformatics. The aim is to identify gene signatures predictive of therapy response and to discover novel therapeutic targets for reprogramming tumor-associated macrophages (TAMs)—immune cells