FLASH-seq was developed to address key limitations of conventional single-cell RNA-seq workflows, especially when full-length transcript information, high sensitivity, and rare cell capture matter. This poster walks through the rationale behind the method, the performance data supporting it, and the improvements that helped bring the protocol into a more practical kit and service format.
Download the poster to explore:
- The advantages of FLASH-seq for full-length scRNA-seq and ultra-low input samples.
- Comparative performance insights, including detected genes, gene-body coverage, and heterogeneous population resolution.
- Protocol improvements that helped reduce workflow duration while maintaining data quality.
