Our Research

Bioinformatics methods to understand personal genomes

We develop fully automated pipelines for genome and exome sequencing analysis: all the way from FASTQ to biological insights.

Computational algorithms for long-read sequencing data

We develop novel methods and software tools for long-read sequencing data on diverse technical platforms, including PacBio, Nanopore, 10X Genomics, Bionano Genomics.

Gene finding for rare undiagnosed diseases

We perform exome/genome sequencing and data analysis to identify disease genes on rare undiagnosed diseases.

Systems biology of multiomics data in complex diseases

We develop and apply systems biology approaches to better understand the biology of complex diseases using genomic, transcriptomic and epigenomic data.