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innovative employers in the region. With more than 6000 employees from 100 different countries, we are helping to build tomorrow's world every day. Through top scientific research, we push back boundaries and
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that the increased risk of UTIs observed in pregnancy may be in part due to differences in the types of E. coli causing the infections, including variations in phylogenetic group, virulence genes and antimicrobial
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We are looking for a motivated and computationally interested student, to work in bioinformatic project on cutting-edge metagenomics and clinical translation. In the 4-year PhD project
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been funded by the Bavarian state and the University of Würzburg. The GSLS is composed of five sections specialising in different aspects of the life sciences and offers a three-year doctoral study
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those using advanced AI, often fail to capture the nuanced clinical and social factors driving these differences, leading to inequitable health outcomes. This is largely because they struggle to leverage
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Medicine and is led by Associate Professor Joakim Esbjörnsson. The group uses various bioinformatics and phylogenetics methods to combine genetic, clinical, and epidemiological data to explain how viruses
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to make a difference in the development of next-generation strain-specific rapid diagnostics, and to help find potential drug and vaccine targets. We offer Lund University is a public authority, which
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through weekly meetings between the doctoral candidate and the thesis supervisors. These meetings will occasionally include other team members (postdoctoral researchers, Master's students). Bioinformatic
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connections to clinicians, patients, and European initiatives such as ERDERA. What sets us apart is our unique position at the interface of bioinformatics, clinical genetics, and patient care. This ensures
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Max Planck Institute for Heart and Lung Research, Bad Nauheim | Bad Nauheim, Hessen | Germany | about 1 month ago
in vitro and in vivo. The Autonomic Research Group (Dr. Karin Ziegler) is looking for a PhD candidate to investigate the molecular fingerprint of sympathetic dysfunction in different disease models