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culturing, pathogenicity assays, molecular biology, genome sequencing and genomic analyses. Experience in field-based assays would be beneficial as large-scale disease screening is planned for March 2026
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for cryogenic electron microscopy (cryo-EM), light microscopy, sequencing, and proteomics. For more information, please visit https://www.helsinki.fi/hilife/bi Where to apply Website https
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use computational approaches to mine natural biodiversity in gene sequences to identify engineering targets to increase lipid content and enhance the water use efficiency. The project will make use
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research using a variety of molecular and microbiological approaches. These include microbial culturing, pathogenicity assays, molecular biology, genome sequencing and genomic analyses. Experience in field
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, including RNA work, protein purification, mammalian cell culture, next generation sequencing genome-wide analyses (ChIP) and mass spectrometry. You will establish and optimise protocols, design and accurately
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cultural history. You are in the process of developing an independent research profile. Your current research includes the preparation of a second monograph (habilitation thesis) aligned with the thematic
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communications. The group is equipped with an extensive array of resources. The group is actively involved in multiple research areas, including: Frontier beam and MIMO technologies for swarm control and ISAC in
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other demands About You We are looking for an experienced researcher to develop and deliver projects that leverage whole-genome sequencing at population-scale to identify rare, high-impact variants
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techniques for example multi-parameter flow cytometry, cell culture, systems serology, ELISpot and ELISA. You should have some knowledge of single-cell RNA sequencing (RNAseq) and other relevant next
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for example multi-parameter flow cytometry, cell culture, systems serology, ELISpot and ELISA. You should have some knowledge of single-cell RNA sequencing (RNAseq) and other relevant next generation sequencing