Core Product Advantages
- Ultra-High Precision with Reliable Data Quality
Boasts an industry-leading Q40 ratio of over 85%, ensuring extremely high sequencing accuracy and enabling sensitive detection of low-frequency mutations. The high-quality sequencing data lays a solid foundation for accurate analysis and decision-making in clinical diagnosis and scientific research.
- High-Speed Sequencing for Rapid Detection
Completes SE50 sequencing in only 6.5 hours, significantly shortening the experimental cycle and efficiently meeting the needs of rapid detection scenarios such as mNGS (metagenomic next-generation sequencing) and PGT-A (preimplantation genetic testing for aneuploidy).
- High Flexibility for Diverse Experimental Needs
Supports flexible run start with no waiting time, greatly improving the utilization efficiency of the sequencer. Fully compatible with mainstream sequencing libraries in the market and supports a wide range of sequencing reagent specifications including SE50, SE100, SE200, PE100 and PE150, adapting to different sequencing read length requirements.
- Wide Dynamic Input Range with Versatile Sample Capacity
Covers a wide dynamic input range and provides adjustable sample loading capacity for a single run (25M Reads/100M Reads). It can flexibly meet the sequencing needs of small sample size for individual research and large sample size for batch clinical detection, realizing efficient utilization of experimental resources.
Diverse Application Scenarios
- Clinical Molecular Diagnosis
Widely applied in tumor precision diagnosis (tissue/blood targeted panel sequencing), reproductive health (PGT-A, NIPT), genetic disease screening and pathogenic microorganism detection (mNGS), providing accurate and rapid genetic testing solutions for clinical diagnosis and treatment.
- Life Science Research
Suitable for high-throughput sequencing research such as WES (whole exome sequencing) and tNGS (targeted next-generation sequencing), supporting the exploration of gene function, disease mechanism and molecular evolution, and providing powerful technical support for basic life science research.
- Environmental Protection
Realizes the detection and analysis of environmental microbial communities through high-precision sequencing, helping to monitor environmental quality, evaluate ecological balance and develop environmental remediation strategies.
- Agricultural Breeding
Supports genomic selection, molecular marker-assisted breeding and genetic diversity analysis of crops and livestock, accelerating the breeding process of high-quality, high-yield and stress-resistant varieties and promoting the development of agricultural modernization.
- Judicial Administration
Provides accurate DNA sequencing data for forensic identification, paternity testing and judicial evidence collection, with high precision and reliability ensuring the scientificity and authority of judicial appraisal results.
System Features
- Compact Desktop Design
Adopts a space-saving desktop form factor, no need for large professional laboratory space, easy to install and operate, suitable for various laboratories, clinical detection centers and research institutions.
- Intuitive Human-Computer Interaction
Equipped with an intuitive control system and user-friendly operation interface, simplifying complex sequencing operation steps, lowering the professional operation threshold, and enabling quick start-up for operators with different technical levels.
- Stable and Reliable Performance
Based on the world’s new core sequencing technologies, the system has stable and reliable running performance, ensuring continuous and efficient sequencing operation, and reducing the failure rate of experimental processes.
- Cost-Effective Sequencing Solution
Balances high sequencing performance and cost control, with flexible sample loading capacity and compatible with mainstream reagents, effectively reducing the single-sample sequencing cost, and realizing high-cost performance for both small and large sample volume sequencing.
| Application Type | Recommended Number of Samples for Single Run | |
| 25M Reads | 100M Reads | |
| mNGS (SE50, 20M Reads/sample) | 1 | 5 |
| tNGS (SE75/BitSeq 90, 1M Reads/sample) | 25 | 95 |
| Tumor targeted panel (tissue, PE150, 1Gb/sample) | – | 30 |
| Tumor targeted panel (blood, PE150, 6Gb/sample) | – | 5 |
| PGT-A (SE100/BitSeq 90, 2M-5M Reads/sample) | 20 | 20-50 |
| NIPT (SE35/SE50, 3.5M-5M Reads/sample) | 5 | 20-28 |
| WES (PE150, 15Gb/sample) | – | 1-2 |


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