Bioinformatic Analysis of Unprecedented Bio-Big Data

With the array of genome technologies we're developing, we're poised to generate vast amounts of bio-big data previously unattainable. Through thorough analysis of these datasets, our aim is to unravel numerous genome mysteries. These encompass inquiries such as understanding the function of every human genetic mutation and elucidating why individuals manifest varying symptoms from similar genetic diseases. Additionally, we seek to explore personalized therapeutic interventions tailored to individual genetic profiles.

2024.04.10

Develop New Sequencing Technologies (Single-cell, Long-read, etc.)

We specialize in pioneering new sequencing technologies based on various next-generation sequencing methods. This encompasses short-read sequencing such as Illumina, long-read sequencing like Oxford Nanopore and PacBio, as well as single-cell-based technologies including 10x Genomics. Our objective is to delve into genome analysis with enhanced depth, accuracy, accessibility, and comprehensiveness. Moreover, we integrate these sequencing advancements with genome engineering technologies to elucidate the dynamics of cellular state alterations.

2024.04.10

Develop Genome Engineering Technologies

We develop a range of genome engineering technologies, notably CRISPR, aimed at addressing the question of 'How to write genome'. Our focus lies in enhancing the versatility, precision, efficiency, and scalability of genome engineering tools. Through our efforts, we aim to establish a comprehensive engineering toolbox capable of generating desired cellular constructs with unprecedented control and efficiency.

2024.04.10

Develop various Genome Technologies to reveal genetic mysteries.

By harnessing cutting-edge genome technologies such as CRISPR, single-cell sequencing, long-read sequencing, and bioinformatics, our laboratory is dedicated to unveiling the hidden secrets within the human genome. We are actively developing genome technologies to enhance our ability to write, read, and analyze genetic information with unprecedented precision and efficiency. With these powerful methods in our toolkit, we possess the capability to both 'WRITE' and 'READ' the genome.

2024.03.19