选择地区语言
This is a mature technical method that uses low-depth whole-genome sequencing to detect chromosomal abnormalities in samples such as patients' peripheral blood, pregnancy miscarriage products/fetal tissue, and chorionic villi. It can identify potential genetic causes for unexplained genetic syndromes and pregnancy losses, assess disease conditions, and assist in clinical diagnosis and treatment.
Platform Advantages
21.5-inch Extra-Large Touchscreen HMI, Full-Process Animated Guidance, and Ultra-Intuitive Control
Multiple throughput options and a range of instrument models—tailored to meet all your needs.
SE75 sequencing takes only 4.5 h, the competitive sequencing speed will keep your project running more smoothly.
Compatible with mainstream libraries on the market, eliminating debugging costs.
Sikun Integrated NGS Solution
Integrates Extraction, Library Construction, and Quality Control in One System.
Eliminates Tedious Operational Procedures, Ultra-Simple Operation.
Reduces analysis time to accelerate
critical clinical and research decisions.
