Struggling with stitching, deconvolving, and visualizing GBs or TBs of data? Interested in viewing large datasets on any computer/laptop?

If so, this webinar may be of interest to you. We’ll discuss how to stitch, deconvolve, and visualize datasets that are even larger than your computer’s RAM with Huygens. We’ll also show you how to work with Huygens’ recent Pyramid File Formats, save BigDataViewer files, and crop regions of interest from large datasets for further processing and analysis. The image shown above is from a 870 GB Zeiss Light Sheet Z.1 dataset that was stitched, vignetting-corrected, deconvolved, and rendered as a MIP using Huygens Professional. Raw data provided by Dr. Dominic Filion, Institut de Recherches Cliniques de Montréal (IRCM), Montréal, Canada.

Register here

If you are a microscopist who's hear more interested in the how than the who, theis webinar is for you. Every microscopist is confronted with the pyramid of imaging trade-offs: balancing signal strength, acquisition speed, field-of-view, photobleaching, sample health, and spatial and temporal resolution. What if experimental showed how to push beyond these limitations - further than you may thought possible. Interested? Register for this webinar below.

Shown is a time series of peroxisomes acquired in collaboration with the Kapitein Lab, Cell Biology, Neurobiology and Biophysics, University of Utrecht, The Netherlands.
Register here