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are encouraged to submit a research proposal that aligns with UCALL's research programme and encompasses multiple areas of law. Your job Over a period of four years, you will conduct a PhD research under the
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project: Computational methods for complex SV detection using sequencing data Main supervisor: Kristoffer Sahlin, ksahlin@math.su.se . Co-supervisor: Adam Ameur, adam.ameur@igp.uu.se . In the Department
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-specific alpha-synuclein A30P human mutation, we will employ electrophysiological techniques, RNA sequencing, proteomics, and histochemical analysis. The findings are expected to provide insights into early
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within a BSc/MSc thesis project. · Ability to effectively and reliably coordinate with the supervisor and multiple collaborators Language skills · Good level both written and spoken
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cell sequencing datasets and to combine these data with AI analyses from bone marrow smears. We aim to analyze mechanisms and also to develop new biomarkers for therapy response and resistance. Job-ID
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for next generation sequencing, single-cell transcriptomics, flow cytometry, mass spectrometry, metabolomics, bioimaging and transgenic mouse work. Strategic research alliances exist with Odense University
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analysis, next-generation sequencing, and small animal models. Salary and social benefits will be determined by the regulations of the German TV-AVH (salary agreement for public service employees
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skilled human operators must acquire and integrate information from multiple distributed sources (e.g., physical and informational environments) to coordinate cognitively (e.g., decision-making) and
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Leibniz Institute of Ecological Urban and Regional Development (IOER) • | Dresden, Sachsen | Germany | about 20 hours ago
conceived research proposals that align with IOER’s research. The programme aims to equip PhD candidates with the knowledge and skills necessary to successfully complete a doctoral dissertation, which may be
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, biochemistry, bioinformatics. The candiate must have a strong foundation in bioinformatics and use of -omics tools. Familiarity with whole genome, exome and transcriptome sequencing workflows is advantageous