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biology as well as in physiology, biophysics, epi /genetics, (bio)informatics, and multimodal data analysis. Over the past decade, our institute has pioneered exome and genome sequencing in order to map
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state-of-the-art approaches, including next-generation sequencing, functional genetic screens, and transgenic model systems. Further information is available on our homepage and via our publications in
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at the participating laboratories, including platforms for NMR, X-ray crystallography, cryo-EM, and light microscopy; the Genome Centre with next-generation sequencing technology; and the Proteome Centre Tübingen
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of crossing protocols for hybridization. Cytogenetic analysis of Bulbosum and barley. Generate and analyze whole genome sequencing data. Analysis, publication, and presentation of research results. Become a
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Alfred-Wegener-Institut Helmholtz-Zentrum für Polar- und Meeresforschung | Oldenburg Oldenburg, Niedersachsen | Germany | about 2 months ago
analyze physiological data, including growth and reproductive performance, under experimental conditions. apply molecular and genomic approaches such as RNA sequencing and DNA sequencing to assess adaptive
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sequencing techniques such as CLIP-seq and TT-seq. Appointment for a minimum of 3 years with a competitive salary (TV-L E13). Hands-on supervision with internal skill building seminars. Close collaboration
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excellent marks and a strong experimental experience in innate immune cell profiling with initial experience in single-cell sequencing analysis is required. Experience with murine disease models is a plus
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fluorescence microscopy, non-invasive imaging (including nuclear medicine), immunomonitoring, deep sequencing and further omics disciplines, biobanking, cytometry and cell sorting, and development of Good
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text analysis and (semi-)automatic labeling, e.g., text/segment classification, sequence labeling, span-based labeling, information extraction (NER/relations, if relevant for coding), transformer
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contributions of these mutations remain poorly understood. Fortunately, advances in genome sequencing and bioinformatics now allow the prediction of deleterious mutations from whole-genome data, enabling