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and international collaborations. The Benson group is focused on combining DNA nanotechnology with selection and sequencing to discover DNA structures that can act as pathogen binders or deliver drugs
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leverage patient-derived material such as post-mortem tissue and cell models, including cellular reprogramming coupled with CRISPR gene editing. We use state-of-the-art sequencing methods e.g. Oxford
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– protein interactions or enzyme optimization. Main responsibilities The successful candidate will use and develop methods within one, or preferably multiple, of the following categories: Sequence library
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fidelity is experimentally challenging and we are using specially-developed methods for library prep for high-throughput sequencing to achieve this. The research involves next-generation sequence library
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experimentally challenging and we are using specially-developed methods for library prep for high-throughput sequencing to achieve this. The research involves next-generation sequence library preparation in
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clonal fate-mapping, flow cytometry, and various in vitro and in vivo stem cell assays. The projects that the new postdoc will primarily be involved in, will apply the same type of DNA sequencing analysis
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Sequencing and associated bioinformatics. Assessment criteria This is a career development position primarily focused on research. The position is intended as an initial step in a career, and the assessment
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opportunity to work with whole-genome sequencing data from over 200 A. pullulans strains, isolated from wild strawberries collected from diverse geographic locations across Europe. The work will include pan
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related to grain protein quality, aroma profiles, and protein structure-function relationship relevant to diverse food applications. The phenotypic data obtained will be aligned with genotypic data (e.g
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apply the same type of DNA sequencing analysis as in a recent publication in which we retrospectively (through phylogenetic analysis) lineage-fate mapped human HSCs (7). Projects will be pursued in part