NNGS-101 is a medium-to-high throughput automated next-generation sequencing (NGS) library preparation system that processes DNA, RNA, and cDNA samples into sequencing-ready libraries through automated fragmentation, adapter ligation, amplification, and purification.
Automated NGS System NNGS-101 is a laboratory instrument that automates DNA and RNA library preparation for next-generation sequencing by performing fragmentation, adapter ligation, PCR amplification, and magnetic bead purification in a controlled workflow.
Automates NGS library preparation workflow
Supports DNA, RNA, and cDNA processing
Handles up to 192 samples per run
Reduces manual handling and contamination risk
Compatible with standard NGS sequencing platforms
Used in research, clinical, and biotech laboratories
NNGS-101 is used to convert biological samples into sequencing-ready libraries for:
Whole genome sequencing (WGS)
RNA sequencing (RNA-seq)
Targeted gene sequencing
Molecular diagnostics
Pathogen detection and surveillance
Gene expression studies
It ensures consistent library quality across multiple samples while reducing manual variability.
DNA, RNA, or cDNA samples are loaded into the system.
Nucleic acids are fragmented into controlled sizes.
DNA ends are repaired and sequencing adapters are attached.
Libraries are amplified to increase yield.
Unwanted fragments are removed using bead-based purification.
Sequencing-ready libraries are collected for downstream analysis.
Manual library preparation is time-consuming, error-prone, and inconsistent.
NNGS-101 automates all major library preparation steps.
Higher reproducibility
Lower contamination risk
Faster turnaround time
Scalable sequencing workflows
Automated liquid handling system
Multi-protocol programmable workflows
Integrated thermal cycling module
Magnetic bead purification system
Sample tracking and barcoding support
Compatibility with NGS sequencing platforms
Pharmaceutical research laboratories
Biotechnology companies
Clinical diagnostics centers
Genomics sequencing facilities
Public health laboratories
Academic research institutions
Choose NNGS-101 if you need:
Medium to high throughput sequencing workflows
Automation beyond entry-level systems (NNGS-100)
Higher sample capacity (up to 192 runs)
Balanced workflow speed and flexibility
Clinical or regulated research compatibility
Whole genome sequencing (WGS)
RNA sequencing (RNA-seq)
Targeted sequencing panels
Infectious disease surveillance
Cancer genomics research
Gene expression profiling
It automates DNA and RNA library preparation for next-generation sequencing workflows.
It processes DNA, RNA, and cDNA samples for sequencing applications.
It supports 24–192 samples per run depending on configuration.
Typical workflow duration is 3–5 hours.
Yes, it supports picogram-level DNA and RNA inputs.
Yes, it generates libraries compatible with standard NGS systems.
It is used in WGS, RNA-seq, targeted sequencing, and molecular diagnostics.
CLIA-aligned workflows
CAP laboratory guidelines
GMP-compatible environments
Manual library preparation kits
Automated liquid handling systems
NGS sequencing instruments
Library QC and quantification systems
Automated NGS System NNGS-101 is a high-performance laboratory automation platform designed to streamline DNA and RNA library preparation for next-generation sequencing. It improves workflow efficiency, reduces manual error, and supports scalable genomic research across clinical, pharmaceutical, and biotechnology applications.
