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-electron microscopy (cryo-EM), particularly in image reconstruction and 3D volumetric analysis of macromolecular structures. Rather than aiming to incrementally optimize existing pipelines, we are interested
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on methodological development in cryo-electron microscopy (cryo-EM), particularly in image reconstruction and 3D volumetric analysis of macromolecular structures. Rather than aiming to incrementally optimize existing
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Arctic charr. About the position The work in the project includes the following tasks: Nucleic acid extraction and optimization of existing protocol Preparation of libraries for high-throughput sequencing
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mathematics, and structural biology. The research environment is embedded in Linköping University and closely connected to SciLifeLab and the national DDLS program. You can read about the workplace here https
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for targeted protein degradation with relevance to cancer biology and therapy. Your responsibilities will include: Designing and conducting biochemical and cell‑based high‑throughput screens Structure‑guided
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. There is growing interest in microsystems that can replicate the local physiology of tumors, providing a platform to identify and optimize therapeutic candidates. Our group specializes in developing
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communication limitations, adversarial conditions, continual and adaptive learning in dynamic environments. The research will combine tools from distributed optimization, stochastic approximation, information
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photodetectors, including thin-film processing and structure–property optimization. In close collaboration with device researchers, you will iteratively improve OPD performance and stability by linking material
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polymers) tailored for organic photodetectors, including thin-film processing and structure–property optimization. In close collaboration with device researchers, you will iteratively improve OPD performance
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-group strategies, stereochemical control, and structural optimization, thereby offering both challenge and creative freedom. Downstream, the monomers will be incorporated into PNA/γPNA oligomers