Michael Chong

Open-ST: High-resolution spatial transcriptomics in 3D

CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions

Calibrated rare variant genetic risk scores for complex disease prediction using large exome sequence repositories

Blood CSF1 and CXCL12 as Causal Mediators of Coronary Artery Disease