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🎯Our Mission
We aim to uncover the genetic and epigenetic mechanisms underlying complex human diseases.
By integrating large-scale multi-omics datasets with advanced computational and systems biology approaches, we seek to understand how genetic variants shape molecular regulation and contribute to disease risk.
🔬 Our Research Focus
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Multi-omics data integration: Genomics, transcriptomics, and epigenomics (ATAC-seq, RNA-seq, single-cell multiome)
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QTL mapping: eQTLs, caQTLs, and their role in gene regulation
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GWAS integration: Linking complex trait variants to regulatory elements and target genes
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Kidney and chronic diseases: Using the kidney as a model system to study genetic regulation, with broader implications for other chronic diseases
🌍 Our Vision
Our research is grounded in basic medical science, but we aim to extend our findings toward medical applications and precision healthcare.
By bridging genomics and medicine, we hope to identify novel biomarkers and therapeutic targets for human diseases.
🤝 Our Values
We value an open and collaborative environment where curiosity, creativity, and persistence drive discovery.
We welcome students and researchers who are eager to learn, explore, and contribute to a vibrant academic community.
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