GS100 Desktop DNA Sequencing System | High-Throughput NGS Sequencer for Precision Genomics
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- High accuracy sequencing with Q40 > 85% data quality
- Fast turnaround time: sequencing completed in as little as 6.5 hours (SE50)
- Compact desktop sequencer design for lab efficiency
- Supports multiple sequencing modes: SE50, SE100, SE200, PE100, PE150
- Flexible run start with no batching delays
- Compatible with mainstream NGS library preparation protocols
- Wide dynamic input range for diverse sample types
- Optimized for low-frequency mutation detection
- Scalable throughput: supports mNGS, NIPT, PGT-A, WES, and targeted sequencing
- Multi-application capability across clinical, research, and environmental fields
Category: DNA sequencer / NGS sequencer
Tags: cancer genomics, desktop DNA sequencer, DNA sequencer, DNA sequencer price, DNA sequencing platform, genomics sequencing system, high-throughput sequencing system, next generation sequencing, NGS sequencer, NGS system for sale, NIPT sequencing, paired-end sequencing, PGT-A sequencing, Q40 sequencing accuracy, single-end sequencing, tumor sequencing, WES sequencing, whole exome sequencing
Brand: Cygnus
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Description
The GS100 Desktop DNA Sequencing System is a compact, high-performance next-generation sequencing (NGS) platform engineered for laboratories that require speed, accuracy, and flexibility in genomic analysis.
Delivering Q40-level accuracy (>85%), the GS100 enables precise detection of low-frequency mutations while maintaining consistent, high-quality data output across a wide range of applications. Its streamlined workflow and flexible run setup eliminate batching delays, allowing users to start sequencing anytime on demand.
Designed for modern labs, hospitals, and research institutions, the GS100 supports multiple sequencing formats including SE50, SE100, SE200, PE100, and PE150, making it a versatile solution for both routine testing and advanced genomic research.
Key Advantages
- Ultra-high accuracy: Q40 > 85% for reliable variant detection
- Fast turnaround: Results in as little as 6.5 hours (SE50)
- Flexible workflow: No batching required, run samples anytime
- Compact design: Space-saving desktop system ideal for labs
- Multi-mode sequencing: Supports SE and PE formats
- Broad compatibility: Works with standard NGS library prep protocols
- High sensitivity: Optimized for low-frequency mutation detection
- Scalable throughput: 25M–100M reads per run
Applications
- Tumor genomics & targeted cancer panels
- Metagenomic sequencing (mNGS)
- Non-invasive prenatal testing (NIPT)
- Preimplantation genetic testing (PGT-A)
- Whole exome sequencing (WES)
- Infectious disease & pathogen detection
- Agricultural genomics & breeding
- Environmental and microbial research
Technical Highlights
- Output range: 25M to 100M reads per run
- Supports single-end and paired-end sequencing
- High-throughput performance for clinical and research workflows
- Designed for precision medicine and rapid detection scenarios
Why Choose GS100?
The GS100 combines clinical-grade accuracy, fast turnaround, and operational flexibility in a compact desktop system—making it an ideal choice for laboratories looking to scale sequencing capacity without increasing complexity.
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