B. Kate Dredge

STAMP enables low-cost, high-throughput single-cell analysis by integrating transcriptomics and proteomics imaging, supporting both single and multimodal profiling of diverse cell types.

The paper investigates whether reported miRNAs in cancer are functionally active, finding many are not incorporated into RISC and lack endogenous silencing capability.

The paper maps alternative polyadenylation changes during EMT in human mammary epithelial cells and identifies QKI's role in regulating APA and gene expression.