Sridar V. Chittur

This study evaluates three cell preservation methods for scRNA-seq across multiple sites, showing concordant cell type results but platform-specific gene expression differences and better granulocyte retention with preservation methods.

This study evaluates how PCR duplication affects RNA-seq data quality across four sequencers, finding that input amount and PCR cycles significantly impact duplication rates, with UMIs effectively reducing duplicates without losing biological information.

The paper compares scRNA-seq platforms and methods using SUM149PT cells treated with TSA, highlighting technical challenges and best practices for low RNA profiling.