NNGS-100 is an automated laboratory instrument that prepares DNA and RNA samples for next-generation sequencing (NGS). It performs library preparation steps such as fragmentation, adapter ligation, amplification, and purification with minimal manual intervention, ensuring high consistency and reduced contamination risk.
Automated NGS Library Preparation System NNGS-100 is a laboratory automation system that converts DNA or RNA samples into sequencing-ready libraries by automating fragmentation, adapter ligation, amplification, and purification steps.
Automates NGS library preparation workflow
Processes DNA and RNA samples
Handles 16–96 samples per run
Reduces manual errors and contamination
Compatible with standard NGS platforms
Used in pharma, biotech, and clinical labs
The system prepares sequencing-ready libraries by performing:
DNA/RNA fragmentation
End repair and adapter ligation
PCR amplification
Magnetic bead purification
All steps are performed in a controlled automated workflow to ensure reproducibility.
DNA or RNA samples are loaded into the system.
Nucleic acids are enzymatically or mechanically fragmented.
Ends are repaired and sequencing adapters are attached.
Libraries are amplified via PCR cycles.
Magnetic beads are used to purify final libraries.
Sequencing-ready libraries are collected for downstream NGS.
Automated liquid handling system
Programmable multi-step workflows
Integrated thermal cycling module
Magnetic bead-based purification
Sample tracking and barcoding support
High reproducibility across batches
Pharmaceutical R&D laboratories
Biotechnology research centers
Clinical diagnostics labs
Genomics sequencing facilities
Pathogen detection laboratories
Academic research institutions
Automation improves:
Reproducibility across samples
Reduction of human error
Lower contamination risk
Higher throughput efficiency
Standardization for clinical compliance
NNGS-100 → Small to mid labs
NNGS-200 → Medium research throughput
NNGS-300 → Large-scale genomic centers
Pharmaceutical companies
Biotechnology firms
Clinical diagnostic labs
Genomics research institutes
Epidemiology surveillance labs
It is a laboratory instrument that prepares DNA/RNA samples for sequencing by automating library construction steps.
It processes DNA, RNA, and cDNA samples depending on workflow setup.
It can process 16 to 96 samples per run.
Yes, it supports inputs as low as picogram-level DNA/RNA.
Yes, it produces libraries compatible with standard NGS platforms.
Typically 2–4 hours depending on protocol.
Yes, it supports CLIA, CAP, and GMP-aligned workflows.
CLIA guidelines
CAP standards
GMP-compliant workflows
Manual library preparation kits
Automated liquid handling systems
NGS sequencing platforms
QC and library quantification tools
Automated NGS Library Preparation System NNGS-100 is designed to streamline DNA and RNA sequencing workflows by fully automating library preparation steps. It enhances reproducibility, reduces manual intervention, and supports scalable genomic research in clinical, pharmaceutical, and biotechnology environments.
