Disease Risk annotation of Genomic and Epigenomic Variants using Machine Learning Approaches

Predicting Time-to-Event and Clinical Outcomes from High-Dimensional Unstructured Data

Maximizing the ability to detect modifying genetic factors of rare complex disorders – Fragile X-Associated Primary Ovarian Insufficiency and Down Syndrome - Congenital Heart Defects

Evolution of Staphylococcus aureus phenotypes

Establishment and Utilization of INTACT-ATAC-seq to Map Cell Type-Specific Gene Regulatory Networks in Plants

Statistical Methods for High-throughput Epigenomics Data

Bioinformatics Methods and Tools for Glycomics

Effects of Life History and Genome Architecture on ssRNA Virus Evolution and Extinction