RESEARCH OBJECTIVES
Hg38-vn
The identification of Vietnamese genomic variants to build custom reference genomes is different from human genome version 38 (hg38).
Long-read data Analysis
Generating long reads and Vietnamese genome reference (VGR) datasets.
Genome Browser
Design a public browser for the VGR genome
SNP chip for Vietnamese
Design a Vietnam-specific SNP chip for genome-based disease prediction
Disease Risk Prediction
Calculation and construction of a list of common and rare genetic variants associated with diseases in Vietnamese (VDV)
Omics data analysis
Conduct a trial that generates 50 WGS and 50 RNA-seq data from patient cohorts for VDV verification
SNP chip application
Assessment of the applicability of the SNP chip in clinical practice along with the typical diagnostic procedure