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mechanisms of the sexual conflict and its resolution. You will combine cutting-edge bioinformatics, genome engineering, and state-of-the-art sequencing technologies to: Identify and characterise consistent
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and spatially complex nature of MRI signals. Each MRI examination involves multiple pulse sequences, with signal acquisition being sensitive to coil placement, sensor geometry, B0/B1 inhomogeneities
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emerged to make meshing more flexible by allowing elements to span across multiple CAD faces without explicitly modifying the geometry. However, these ideas have not yet been developed in high-order
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unified artificial intelligence (AI) model capable of segmenting 3D medical images from standard clinical scans and generating 3D meshes across multiple imaging modalities. The project will also investigate
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harnessed to kill breast cancer cells. Breast cancer is the most common form of cancer in women and novel therapies are needed to improve disease outcomes. We will sequence RNA from a cohort of more than 300
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pseudorange correction through multiobjective optimisation. The research will explore multiple classes of constraints that will be embedded as objectives: Internal pseudorange consistency: ensuring
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the drivers behind this public health issue have not been identified. In this project, we will use a dataset of C. difficile genome sequences to generate a nationwide population snapshot of
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for antibiotic prescription. Novel, rapid, point-of-care, precise and easily interpreted diagnostic tools are required to tackle this challenge. Direct sequencing of nucleic acids from patient samples can be rapid
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SD- 26053 PHD IN ULTRA-FAST MACHINE-LEARNING INTERATOMIC POTENTIALS FOR NANOINDENTATION OF TIC MA...
nationalities represented in our workforce Diverse and inclusive work environment empowering our people to fulfil their personal and professional ambitions Gender-friendly environment with multiple actions
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up analytics including HPLC, LC-MS and GC-MS Protein expression, purification and characterization using biochemical and biophysical assays Variant identification using next generation sequencing