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sequencing, spatial and single-cell multi-omics. This research could deepen the fundamental knowledge and promote translational/preclinical development. You must have a proactive and adaptable approach to work
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they are streamlined, inclusive and aligned with our future People Service Model. Act as product owner, shaping a recruitment service that is enabled by digital solutions, including AI and automation, to deliver a
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. The Deputy Director will work with the Director to provide intellectual leadership and strategic direction for the centre, alongside leading a programme of impactful research that aligns with the centre’s
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Cancer) study, a Cancer Research UK–funded programme led from the University of Oxford. The project aims to uncover how the sequence of genetic mutations in colorectal cancer drives changes in stem cell
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authorisations worldwide. If you are passionate about conducting high-impact research that drives meaningful change, we encourage you to apply. You will exploit a ground-breaking long-read sequencing metagenomic
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for facilitating effective communication with, and interaction between, the Hub’s various stakeholders, both internal and external. This will involve managing multiple communications channels and planning, creating
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preimplantation genetic testing, molecular sequencing, and bioinformatics. If you are eager to contribute your expertise and inspire the next generation in these cutting-edge fields, this role offers a unique
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Colorectal Cancer) study, a Cancer Research UK–funded programme led from the University of Oxford. The project aims to uncover how the sequence of genetic mutations in colorectal cancer drives changes in stem
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, bioinformatics, and data science. You will design and deliver statistical analyses using large-scale electronic health records and pathogen sequencing data to improve infection diagnosis, management, and
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close to completing) a PhD in statistical genetics, computational biology, bioinformatics, or a related quantitative discipline, with proven expertise in the analysis of large-scale sequencing data and