531 computer-programmer-"FEMTO-ST"-"FEMTO-ST"-"FEMTO-ST" Postdoctoral positions in United Kingdom
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Field
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aims to achieve reliable genome design and synthesis – engineering cells to have specific functions – which will be a major milestone in modern biology. A dedicated social science program will support
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Join the Oxford Martin Programme on Forecasting Technological Change at the University of Oxford, led by Dr François Lafond, Prof J. Doyne Farmer, and Prof Max Roser. This pioneering programme aims
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with an international reputation for excellence. The Department has a substantial research programme, with major funding from Medical Research Council (MRC), Wellcome Trust and National Institute
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Deadline 16 Dec 2025 - 00:00 (UTC) Type of Contract Other Job Status Full-time Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Is the Job related to staff position
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project lead Dr Janice Attard-Johnson and with co-lead Professor Sarah Bate to prepare materials, design and programme experiments, participant recruitment and data collection, develop and conduct
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interdisciplinary research programme investigating how immune mechanisms contribute to psychiatric and neurological disorders. The project combines human induced pluripotent stem cell (iPSC)- derived neuronal and
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our multidisciplinary team working at the interface of epidemiology, data science, and public health policy. The successful candidate will develop and apply advanced mathematical and computational
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-in-cell computer codes hosted on local and national high-performance computing clusters; establishing all-optical diagnostics to map temperature evolution in plasma accelerators; exploring novel inter
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proof-of-principle repetition-rate and staging experimentation. The successful candidate will perform duties that include developing/using particle-in-cell computer codes hosted on local and national high
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(IDH1/2) genes and this project focusses on how these mutations re-program liver cells, in the context of biliary cancer. We are using CRISPR-edited human cells and novel transgenic models in mice