Tue, Jun 16|
Illumina Experience 2020
See how our new and upcoming library prep kits will allow you to explore new science across a variety of current and emerging applications, whether it’s bulk RNA-Seq, whole genome sequencing or exome sequencing.
Time & Location
Jun 16, 2020, 10:00 AM – 2:30 PM GMT+2
About the Event
To present our new products to the genomics community in Europe, the Middle East and Africa, we will host a virtual event on June 16, 2020. Join us to learn how Illumina’s new and innovative library prep solutions coupled with the recently launched NextSeq™ 1000 and NextSeq™ 2000 platforms can accelerate your research.
From presentations by Illumina’s R&D and applications experts to interactive meet-and-greets with the Illumina team, to virtual booths by guest companies – do not miss this gathering of the genomics community.
Innovations in next-generation sequencing (NGS) are helping the genomics community ask, and answer increasingly complex scientific questions. Across the spectrum of genetic disease research, single-cell studies, pathogen detection, profiling of tumor microenvironment, and other emerging applications, researchers need sequencing power to help fuel larger studies of more samples at greater sequencing depth and at a lower cost.
To support this expansion in research, Illumina is committed to enabling the exploration of the genome, transcriptome, and epigenome by providing users with innovative advances in technology and systems. Over the last 20 years, Illumina, working closely with the scientific community, has led the charge to improve sequencing capabilities across the entire workflow, making it easier to use while driving down costs.
The presentations will be held in English, but during the event, various team members will be able to answer your questions in English, French, Italian, German, and Spanish.
Please see the agenda tab at the top of the page for more information.
Register now to secure your space at this virtual event