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cells (iPSC), whole genome sequencing, genome wide association studies, epidemiology, experimental psychology, psychometrics, gaze-tracking, and obstetrics. We welcome applications from highly motivated
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and diagnosis of common and rare diseases, using multi-omics and/or long read sequencing approaches. Responsibilities include optimizing data workflows, ensuring data quality, and supporting lead
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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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for personalised breast cancer treatments. Analyse data from cutting-edge technologies (e.g. matched tumour-normal whole genome sequencing, bulk and single-cell RNA sequencing of the tumour microenvironment, spatial
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Generation Sequencing (NGS) core facility. This facility supports the general NGS needs of our researchers and is currently expanding into delivering spatial genomics services. You will be responsible
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RNA or ribosome-associated structures. Computational and Bioinformatic Analysis Handling and interpreting large datasets, sequence conservation, RNA structure modelling, and more. You will be supported
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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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a city in an unstable environment at the centre of the Indian Ocean, in which arose a diverse society, generating an abundance of cultural production and a sequence of violent politics. We are looking
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. This post will involve the use of cutting edge biochemical, proteomic, next generation sequencing and ribosome foot printing technologies. This position is available for an immediate appointment. Candidates
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ability to lead diverse but complementary projects to completion is essential. Experience in in vivo experimentation with rodents, RNA sequencing (or other high-throughput technologies), bioinformatic