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will be the analysis of virus sequence data generated through our surveillance activities. Surveillance will be based on next-generation sequencing of viral RNA/DNA extracted from wastewater samples. We
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, genetic, and DNA methylation analyses to patient-derived samples and disease models. Working closely with a dynamic and multidisciplinary team of clinicians and scientists, they will help generate and
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take a lead role in conducting wet lab experimentation, applying state-of-the-art single-cell multiomic approaches, including transcriptomic, genetic, and DNA methylation analyses to patient-derived
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myeloproliferative neoplasms (MPNs). You will take a lead role in conducting wet lab experimentation, applying state-of-the-art single-cell multiomic approaches, including transcriptomic, genetic, and DNA methylation
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research focuses on two areas: (1) how epigenetic memory—via Polycomb silencing and DNA methylation—is established and maintained, and (2) pattern formation in sub-cellular systems, particularly crossover
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pathogens as a model system. There are two post-doctoral research positions and one PhD studentship associated with Dr. McDonald’s UKRI Future Leader Fellowship, which will explore the cell biology
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signalling in DNA damage and/or immunity responses. The post-holder will be responsible for managing own academic research, adapting existing and developing new scientific techniques and experimental protocols
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. It is essential that you hold a PhD/DPhil with clear relation to biology together with relevant research experience in academia or industry. You will have experience with cancer genomics, including
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of Pathology, University of Oxford to study interplay between ADP-ribosylation and ubiquitination signalling in DNA damage and/or immunity responses. The post-holder will be responsible for managing own academic
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imaging data - Developing new methods for inference of copy number alterations from single-cell DNA sequencing data - Analysing patterns of single-cell copy number variation to identify mechanistic