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Field
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Experience: Experience with processing, imaging and analyzing fluorescently labeled samples, preferably with commercial microscopes and open-source analysis software such as ImageJ/Fiji, cellpose, and/or
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interactions. The facilities include full-service histology, microscopy (fluorescent, confocal, and electron), tissue culture, animal surgery and imaging rooms, providing a rich scientific environment for basic
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culture, fluorescence confocal microscopy, transmission electron microscopy, digital image analysis and statistics. The capacity to thrive in a highly collaborative research laboratory environment is
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-Saclay region and is easily accessible by public transportation from Paris. More information is available at https://www.ip-paris.fr . The candidate will join the doctoral school of the Institut
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The International Institute of Molecular Mechanisms and Machines Polish Academy of Sciences | Poland | about 2 months ago
, chromatin organization, and cell fate. Our research combines molecular and cellular biology, quantitative fluorescence imaging, protein biochemistry, proteomics, and functional genomics to uncover fundamental
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Experience: Experience with processing, imaging and analyzing fluorescently labeled samples, preferably with commercial microscopes and open-source analysis software such as ImageJ/Fiji, cellpose, and/or
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on developing probabilistic latent-variable methods for large and structured biological data, with applications in genomics, spatial transcriptomics, and fluorescence imaging. High-dimensional and structured
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interactions. The facilities include full-service histology, microscopy (fluorescent, confocal, and electron), tissue culture, animal surgery and imaging rooms, providing a rich scientific environment for basic
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of studying these artworks, and (c) to synthesize scientific findings to address art historical questions and preservation challenges. Use advanced imaging technologies and scientific methods to uncover
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fluorescent labeling tools and automated particle-tracking methods, to directly measure membrane fluxes during development. These approaches will enable the quantification, at the level of intracellular