Long-Read Sequencing Technology

Advanced next-generation sequencing technology platform for professional diagnostic and research use. The system provides high-throughput genetic sequencing capabilities for medical applications.

An advanced sequencing platform incorporating fluorogenic optical chemistry and error-correction mechanisms. LumoSeq enables long-read sequencing with high accuracy and rapid speed for genomic research and molecular diagnostics.

Proprietary surface fluorescence sequencing technology that enables detection and sequencing of weak DNA signals with extremely high sensitivity. The platform provides precise and rapid genetic analysis through innovative optical sequencing methodology.

A mid-to-high throughput sequencing platform based on cPAS (circular Polymerase Amplification Sequencing) technology. It generates high-quality data through DNA nanoball (DNB) preparation to preserve original genomic information with minimal bias. The system offers flexible sequencing modes supporting both mid and high-throughput read options with customizable read lengths. It features convenient operation with automated cartridge loading and rapid analysis through the integrated visualization system, with broad applications in whole genome, whole exome, and targeted sequencing across multiple clinical domains.

Ultra-high throughput next-generation sequencing instrument capable of 14Tb per run with 9Tb per day productivity. Features innovative sequencing chemistry, AI-based recognition algorithms, and patterned array flow cell technology achieving Q40 scores ≥90% accuracy.

Advanced genetic sequencing system utilizing surface-restricted fluorescence technology for high-sensitivity DNA signal detection and analysis. Designed for precise and rapid gene sequencing applications in research and diagnostic settings.

HapSeq-2000 is a domestic all-in-one benchtop gene sequencer developed by HaploX Biotechnology. It features innovative design, advanced sequencing chemistry technology with reversible terminator sequencing and synthesis-by-sequencing (SBS) methods, and integrated on-board bioinformatics tools. The system achieves Q30 scores up to 90% and supports flexible sequencing applications including whole genome sequencing, metagenomics, spatial transcriptomics, and pathogen detection. It includes integrated DRAGEN Bio-IT platform for primary and secondary analysis, producing standard data results within 2 hours, with data output ranging from 10Gb to 540Gb and read lengths from 1x50bp to 600bp (2x300bp).

Semiconductor-based sequencing system utilizing nanopore technology for genomic analysis. Suitable for multiple applications in molecular biology, offering cost-effective and rapid sequencing solutions.

High-throughput DNA sequencer for rapid genomic analysis in clinical and laboratory diagnostics. Enables identification of genetic variations, pathogenic mutations, and infectious agents through next-generation sequencing technology. Delivers accelerated sample processing and comprehensive results to support precision medicine and disease diagnosis.

S100 is a benchtop gene sequencing platform that enables long-read, high-accuracy genomic analysis for research and clinical diagnostics. The system utilizes proprietary fluorogenic technology and error-correction algorithms to deliver Q40-level data quality, supporting applications in disease diagnosis, microbial detection, and environmental screening.

A sequencing platform utilizing Surface Restricted Fluorescence Sequencing technology for genomic analysis and research applications. The platform is designed for efficient processing of samples including circRNA and detection of RNA modifications such as m6A.

A benchtop sequencer based on Cygnus Biosciences' proprietary sequencing technology, featuring long read length, fast sequencing speed, and high accuracy. It achieves data quality up to Q40, is compatible with mainstream sequencing platforms, and offers flexible power supply options, wireless connectivity, and no special installation requirements to meet most laboratory sequencing needs.