On-demand webinar
Automate to accelerate: How to streamline single cell sequencing with automation
Download this webinar to learn how the Opentrons Flex can be paired with Parse Biosciences technology to streamline single cell sequencing.
Single-cell RNA sequencing (scRNA-seq) is a powerful technique for teasing apart the heterogeneity between cells in a population and identifying subtypes within a sample.
Parse Biosciences’ Evercode™ technology leverages the proprietary split-pool combinatorial barcoding to uniquely label individual cells, enabling scalable and high-quality single cell data.
This webinar will demonstrate how the whole workflow, from fixation to library preparation, can be automated efficiently on the Opentrons Flex. This webinar will also present data that shows high-quality scRNA-seq libraries generated from peripheral blood mononuclear cells (PBMCs).
Download to learn:
- How Parse Biosciences’ Evercode™ technology can provide scalable, high-quality scRNA-seq data through split-pool combinatorial barcoding
- How you can leverage the Opentrons Flex liquid handling platform to automate popular genomics workflows, including scRNA-seq
- How automating the entire Evercode WT workflow on Opentrons Flex can reduce needed hands-on time by over 10 hours for a single experimental run
Who should access:
- Scientists in academia, core labs, and pharma and biotech who are leveraging transcriptomics techniques
- Scientists in academia, core labs, and pharma and biotech who are leveraging transcriptomics techniques
Access now!
Subject to your consent given above, by clicking on “register”, Opentrons may use your personal information to communicate with you for marketing purposes. All information you provide in this site will be governed by our Privacy Policy.