LUNCH AND LEARN SEMINAR AT THE UNIVERSITY OF GOTHENBURG

Scalable, Accessible Single Cell with Parse Biosciences' Evercode

26 September, 11:30 - 13:30 CEST

Assembly Room Birgit ThilanderMedicinaregatan 3
Gothenburg, Sweden

LUNCH WILL BE PROVIDED

Single cell RNA-Seq has become a required tool in today's genomics research. Droplet-based approaches are effective, but struggle against flexibility, high costs, and scale. Parse Biosciences' Evercode technology enables you to conduct scalable single cell with no instrument required.

Here's how Parse can help streamline your research:

Evercode Whole Transcriptome kits are scalable from 10K cells up to 1 million cells across 1-96 samples
No specialized instrument needed to barcode or sequence libraries
Applications include Immune profiling, TCR and BCR assays, CRISPR libraries
Training and support included via a dedicated field application science team
Access to Trailmaker, our user-friendly cloud platform, to take FASTQ files through to manuscript-ready figures

Can't make it in person? A Zoom link will be provided the day of the seminar. See you then!

Register here

Agenda

Overview of Evercode, Scalable Single Cell Without an Instrument
Paula Garcia
Sample Preparation Considerations
Alex Stretton
Data Analysis with Trailmaker, from FastQ to Publishable
Ashwini Girish Kumar
Benchmarking Evercode v3 scRNA-seq Data in Human Pancreatic Islet Cells
Joan Camuñas-Soler, PhD
NGS Research Services, Clinical Genomics, SciLifeLab, Gothenburg
Catarina Mörck, PhD and Sanna Abrahamsson