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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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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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Application dates Applications close31 August 2025 What you'll receive You'll receive a scholarship top-up for $10,000 per annum, for up to 3.5 years. The end date will be aligned with your existing
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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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implement a combination of metagenomic sequencing techniques to comprehensively characterise baseline levels of microbial pathogens in wastewater and surface water and compare our findings with data
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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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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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Leibniz Institute of Ecological Urban and Regional Development (IOER) • | Dresden, Sachsen | Germany | about 6 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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methods for single-cell data analysis (tools developed by the team : https://github.com/cantinilab ). Single-cell high-throughput sequencing, extracting huge amounts molecular data from a cell, is creating
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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