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‐sharing agreements. Data analysis & interpretation: Process and interpret high‑throughput sequencing outputs to assess biodiversity patterns across multiple MPA sites. Comparative evaluation: Critically
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multi-disciplinary approaches to answer these key questions including; immunology, oncology (in vitro model-organoid systems, ex vivo tissue culture), microbiology, next generation sequencing (16S seq
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, which aims to identify novel targets for male contraception. In this research project, we will be using cutting edge sequencing datasets (e.g. single cell RNA-seq, methylome) as well as cell and tissue
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Deutsches Zentrum für Neurodegenerative Erkrankungen | Bonn, Nordrhein Westfalen | Germany | about 2 months ago
and Epigenomics (PRECISE) at the DZNE is looking for a full-time (39 hours per week) scientist working at PRECISE in the areas of next-generation sequencing, single-cell OMICS, and to support the
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., 2020; Hersperger et al., 2024). Our lab employs a combination of approaches such as genetic screens, single nuclei RNA-sequencing, live imaging, fate mapping approaches and reporter lines, and
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Deutsches Zentrum für Neurodegenerative Erkrankungen | Gottingen, Niedersachsen | Germany | 21 days ago
studies (behavioral and endpoint analyses, reproducibility, standardized tests). Advanced skills in the analysis of next-generation sequencing data (RNA-seq), including the use of common bioinformatics
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of sequencing-driven, microbiological, and immunological approaches on gnotobiotic mouse models and patient cohorts (e.g., El Mouali et al., Cell Host Microbe, 2024; Osbelt et al., Nature Microbiology, 2024
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host chromatin pathways (DFG Research Unit DEEP-DV, FOR5200). The group uses experimental infection systems, an array of high-throughput sequencing methods (e.g., scRNA-seq, ChIP-seq, CUT&Tag, ATAC-Seq
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opening at the clinic for the Kardiology, Klaus Tschira Institute for Integrative Computational Cardiology. Project: Dynamic RNA modification changes via Nanopore Sequencing Location: University Hospital
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to improve patient care. These efforts are enabled by our department's world-leading collection of brain tumour samples which are complemented by DNA methylation, DNA and RNA sequencing as well as clinical