Regulatory Variants:
Uncovering Regulatory Variants Related with DiseasesClinical Genome Informatics:
We focus on developing several NGS products, databases, genome repositories, and products to interpret personal genome including complex and medallion diseasesResilience Project:
identified unexpected heroes in over 600,000 individualsPersonalized cancer therapy project:
built a pipeline to sequence, analyze, and interpret tumor samples and created clinical reports to recommend personalized therapeutics, clinical trials and vaccine for patients with a wide variety of tumor typesDisease network:
build disease networks through integrating genetic, EMR, and literatureDiagnostic/Prognostic assay development:
developing methods to integrate and translate various molecular measurements in the public repositories into biomarkers for the diagnosis of diseaseActiVar:
Drug target, risk factor, and disease risk profile identification from comprehensive disease variants from Hadoop-based text mining, curation, and public repositories from curated databasesClinLabGeneticis.t:
ClinLabGeneticist is disease-agnostic and can be used to explore variants associated with various rare genetic disorders although it could also work, with some adjustments, for germline cancer assessments
About Our Lab
We have been working on translational bioinformatics and personalized medicine from four directions. 1). To integrate genome sequencing, exome sequencing, and RNA-Seq data to drive personalized cancer therapy. 2). To predict personal risk of disease through integrating genome sequencing, electronic medical records, and environmental factors. 3) To integrate and translate various molecular measurements in the public repositories into biomarkers for the diagnosis of disease. 4). To discover the causal variants, pathway, and mechanism to illustrate human disease through integrative genomics.