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Nanopore sequencing, ChIP-seq, and Hi-C, to probe plant genomes and centromeres. The project will involve both wet-lab based functional genomics approaches, together with dry-lab based bioinformatics
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mutations occur at preferred DNA motifs, there is substantial variation in mutation frequency between motifs, leading to the hypothesis that there exists a sequence “grammar” regulating motif mutability. Our
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of liver metastases and 2) ex-vivo MRI of human liver tissue specimens. You will be responsible for the sequence implementation, data acquisition and analysis, including biophysical models of liver tissue
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biophysical forces at play, the similarities and differences across animals, and how IVF clinics can better decide which embryos to implant. This project will be aligned with the aims and objectives
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which they operate. We have established collaborations across the globe and built a research programme that leverages high throughput, high-resolution sequencing platforms and novel analytical methods
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Assistants is £32,546 - £35,116 and for Research Associates this is £37,174 - £45,413 per annum. Suitable candidates should have previous experience of genetic analysis of large scale genome sequence data and
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We are inviting applications for an exciting new post for a Research Assistant to work with Dr Megan Kirk Chang on an interdisciplinary research program on the Oxford Health BRC Preventing Multiple
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programme focussed on understanding the genetic basis of undiagnosed mitochondrial and neurogenetic disorders using whole genome and single cell sequencing, animal and cellular models, including human
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(£2.5M in total) and aligned to the NIHR Applied Research Collaboration (ARC) South London as co-funded research infrastructure. The KIS programme will continue to support scalable projects and programmes
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(notably MCP, A2A). Note that the successful candidate will work in collaboration with two other postdocs on a closely aligned project “Rethinking multi-agent systems in the era of LLMs”, funded by