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

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Location

SciLifeLab Uppsala

3 Husargatan

752 37 Kåbo

Sweden

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

About this Event

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.

Keynote Speaker:

Gema Fuerte, MSc, Mission Bio

Agenda:

13.00 -13.20: Introduction by the 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

Address:

Science for Life Laboratory (Navet) BMC, Husargatan 3, 752 37 Uppsala, Sweden

Room #:

E10:1307-1309

Partners:

National Genomics Infrastructure

SciLifeLab

Date and Time

Location

SciLifeLab Uppsala

3 Husargatan

752 37 Kåbo

Sweden

View Map

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