Our Research
From uncovering the genetic underpinnings of rare inherited disorders to dissecting the complexities of multifactorial traits and diseases, our research spans the full spectrum of genomic science. We are driven by a central goal: to understand how variations in DNA shape biology, influence health, and contribute to disease. By bridging fundamental research with translational applications, our work seeks to transform genomic insights into meaningful advances for medicine, biotechnology, and beyond.
Our laboratory is equipped with state-of-the-art sequencing platforms, robust bioinformatics pipelines, and high-performance computational infrastructure that enable us to generate, analyze, and interpret vast amounts of genomic data. Leveraging these powerful tools, we investigate biological questions at multiple scales—from single-cell genomics to population-level studies—integrating experimental, computational, and statistical methods to illuminate the architecture of life’s most fundamental code.
Whether unraveling the mysteries of human genetics, probing the hidden diversity of microbial communities, or decoding the evolutionary history of plants and animals, our interdisciplinary team embraces collaboration across biology, medicine, and data science. Together, we are pushing the boundaries of discovery, developing innovative approaches to explore the genome, and revealing insights that advance our understanding of health, disease, and the natural world.
Current Projects
Our research spans multiple areas of investigation, from basic science to clinical development.
