13 algorithm-development-"Multiple"-"Simons-Foundation"-"Prof"-"Prof" scholarships at University of Cambridge
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Supervisor: Professor Florian Markowetz Course start date: 1st Oct 2026 Overview Professor Florian Markowetz wishes to recruit a student to work on the project entitled: “Development and
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developments such as novel algorithms to support logistics operations, novel automation approaches or the design and development of new digital support tools for logistics providers. Significant flexibility
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, develop business cases and more. At the 6-month point, students progress onto their interdisciplinary PhD research project, supervised jointly by two academics from two research groups. Usually, supervisors
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both sites. The project sits at the interface of cell line engineering, protein science and machine learning and you will receive advanced training in these areas while developing methods to accelerate
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to cancer biology, as well as a strong commitment of developing and using new tools to address cutting-edge questions in these fields. This studentship is embedded within the piRNA team, consisting of both
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will be defined, decomposed and assessed through attention to artefacts and practices across a range of sectors and disciplines. Focusing on the automotive context, the project will develop a
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of our approach is the innovation of novel methods to investigate genome function. For example, we have recently developed ways to map the binding of nucleic acid-interacting drugs and small molecules
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therapy (Simpson et al. in preparation*). When these local metabolic / immunologic changes happen during pancreatic cancer evolution remains unknown. More importantly, whether these spatial changes can be
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target, since all known treatment resistance mechanisms are downstream of, and dependent on FOXA1. However, FOXA1 has been a difficult protein to study for technical reasons. We have developed a novel tool
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Ascl1 are important. We have undertaken a comprehensive discovery experiment to identify all the proteins that can physically interact with Ascl1, using a method we developed called RIME (Rapid