About this event
In the last few years, single cell approaches have moved into the mainstream, leading to rapid progress in the understanding of complex biological systems. However, these approaches are extremely difficult to perfect. It’s often difficult to derive high quality data, particularly from cell types and tissues that are harder to process.
In this webinar, we will show you every step of a particularly challenging single cell project, including often neglected pilot experiments, taking you from the initial research questions to the final results.
This webinar will present a fascinating, extremely challenging case study that focused on celiac disease (CD), one of the most common auto-immune disorders. Single-cell RNA sequencing can improve our understanding of the human gut function, both in health and across the spectrum of diseases, including CD.
Here you will embark upon a research journey alongside Luigina De Leo, as she navigates through her investigation towards the generation of impactful final data and a successful outcome. Unlike traditional presentations that showcase only polished final results, this webinar will reveal the entire investigative process, including the challenges faced and the strategies employed to overcome them.
In addition, webinar attendees will have the opportunity to engage in discussions, sharing their own experiences and obstacles encountered in single cell sequencing. As a result, this webinar will be informative and interactive, offering a unique blend of scientific learning and collaborative exploration.
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Luigina De Leo, Research Scientist, Laboratory of Pediatric Gastroenterology, Institute for Maternal and Child Health IRCCS Burlo Garofolo
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This webinar has been produced with the kind support of Singleron Biotechnologies and Macrogen. You can find out more about the technologies outlined in this webinar by visiting the Singleron Biotechnologies and Macrogen websites.
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Front Line Genomics is a genomics-focused media company, with a social mission to deliver the benefits of genomics to patients faster. We organise the Festival of Genomics, digital events and webinars. We also produce reports and operate a content-rich website.