Moving from Bulk NGS to Precision Sequencing with Single-Cell Genomics


Moving from Bulk NGS to Precision Sequencing with Single-Cell Genomics: Resolving Heterogeneity in Blood and Solid Tumors

 

Seminar Abstract
Where single-cell sequencing methods have improved our ability to better characterize tumor heterogeneity, current modalities are unable to determine both genotype and phenotype from the same cell simultaneously. Discover how the Tapestri Platform enables co-detection of SNVs, CNVs and proteins from the same cell using a single workflow, providing a true multi-omics approach for deeper insight into systems biology and patterns of tumor evolution, therapy response, and resistance. Also join us for a discussion on future multi-omic capabilities.

13.00 -13.20
Introduction by the SciLifeLab National Genomics Infrastructure
Jessica Nordlund, Facility Director

13.20- 14.30
Moving from Bulk NGS to Precision Sequencing with Single-Cell Genomics: Resolving Heterogeneity in Blood and Solid Tumors
Gema Fuerte, European Field Application Specialist, Mission Bio

14.30-15.30
Opportunity for discussions with representatives from NGI and Mission Bio

 

Venue
E10:1307-1309, Science for Life Laboratory (Navet) BMC, Husargatan 3, 752 37, Uppsala, Sweden

 

Registration and more information