Quang Vinh Phan

This paper uses prime editing to classify LDLR variants by measuring their impact on LDL-C uptake, reclassifying many previously unclassified variants.

The paper introduces ACCESS-ATAC, a method that improves TF binding site prediction resolution and reveals allele-specific co-occupancy patterns in HepG2 and K562 cells.

This paper improves variant effect quantification in base editing screens by integrating genotypic and phenotypic data using a Bayesian network called BEAN.