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Field
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long-read nanopore sequencing and deep mutational scanning of the screening output. This approach selects new, efficient enzymes, but also generates unique sequence-function datasets that will be
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streams across the continent, multiple differently coloured catfish communities coexist, forming diverse mimicry “rings.” This project will use whole-genome resequencing to tackle three key questions: Which
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allowing elements to span across multiple CAD faces without explicitly modifying the geometry. However, these ideas have not yet been developed in high-order settings, where curved elements, geometric
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the mesh, which is computationally expensive and environmentally inefficient, or by running multiple successive simulations to iteratively adjust the mesh. Both approaches raise computational cost, energy
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to post-doctoral level. They will receive hands-on training in fluorescent microscopy, fungal culture, transcriptomics, next-generation sequencing, molecular microbiology, nuclear magnetic resonance
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long-read nanopore sequencing and deep mutational scanning of the screening output. This approach selects new, efficient enzymes, but also generates unique sequencefunction datasets that will be
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to the interior of the cell. GPCRs are involved in multiple physiological process including cell growth, neurotransmission, metabolism & immune response; they can misfunction in disease and consequently have served
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results align with the abundance and expression of diatom ppRHO genes in the surface oceans. Research methodology Objective 1: Identify the subcellular localisation of two different ppRHOs isolated from
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. Why this project? As we age, many of us face multimorbidity, where multiple diseases strike together, often driven by chronic, low-level inflammation damaging our tissues. Current treatments don’t
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Student Development The successful applicant will gain expertise in: Biophysical imaging (AFM, microscopy) Microbiology and molecular biology RNA sequencing and data analysis Interdisciplinary collaboration