Skip to Content
Next Generation Sequencing (NGS)

HOME  /  APPLICATIONS & TECHNIQUES  / 

DNA / RNA (Nucleic acids) Next Generation Sequencing (NGS)
Share

Next Generation Sequencing (NGS)


Analis propose the NGS sequencer from GeneMind and provide end-to-end NGS solutions from DNA extraction and library preparation to sequencing, bioinformatic analysis, and final report generation.

Request more information

NGS: Revolutionize Genetic Analysis with Rapid, Cost-Effective Sequencing

Next Generation Sequencing (NGS), also referred to as second-generation sequencing, has transformed genetic research by enabling the parallel sequencing of millions of DNA fragments. This technological breakthrough has dramatically reduced sequencing costs while expanding analytical capabilities across research, clinical, agricultural, and environmental fields.


Today, NGS is a cornerstone technology for laboratories seeking high-throughput, scalable, and reliable genomic insights.


Key Applications of NGS

  • Clinical Research: Oncology, pathology, immunology, microbiology, virology, and translational research.

  • Agricultural Sciences: Crop improvement, disease resistance studies, plant and animal genomics.

  • Environmental Sciences: Biodiversity assessment, microbial ecology, pollution monitoring.

  • Forensic Science: DNA profiling, identity testing, and crime scene investigations.

With its rapid turnaround times and cost-effective scalability, NGS continues to redefine how we understand genetics and its impact on health, food security, and environmental sustainability.

 

GeneMind NGS Sequencers - Integrated Platforms for End-to-End Sequencing

One Platform. One Provider. Complete Workflow.

GeneMind delivers high-accuracy, cost-efficient NGS sequencing solutions with comprehensive after-sales service and technical training. The fully integrated workflow—from sample preparation to bioinformatics analysis and reporting—is provided by a single manufacturer, eliminating third-party dependencies.


Advantages of GeneMind NGS Platforms

  • Cost-effective solutions for diverse research and diagnostic applications
  • High sequencing accuracy and robust data quality
  • Compatibility with mainstream NGS library preparation kits
  • Flexible throughput options across different instrument models
  • Fully integrated end-to-end workflows
  • Comprehensive bioinformatics support


GeneMind platforms are designed to simplify implementation, reduce operational complexity, and ensure long-term performance in modern genomic laboratories.


 GeneMind NGS Sequencing Platforms

See NGS Products See NGS Applications

GeneMind NGS Sequencing Platforms by Throughput

GeneMind offers a comprehensive portfolio of NGS sequencers with scalable throughput, delivering data outputs ranging from 24 Gb up to 14 Tb per run. These platforms are designed to meet the needs of laboratories of all sizes — from small academic research groups to ultra-high-throughput sequencing centers.

Whether your priority is flexibility, scalability, or large-scale genomic production, GeneMind provides a solution aligned with your sequencing volume and workflow requirements.

FASTASeq S 
Rapid NGS Sequencer for Time-Critical Applications

LOW Throughput

2 Gb to 24 Gb

​Genemind NGS Sequencer FASTASeq S

mNGS / tNGS / NIPT / PGT-A / pathogen quick test


Learn More about FASTASeq S

FASTASeq  300 
Desktop High-Throughput NGS Sequencer

MEDIUM Throughput

5 Gb to 150 Gb

​Genemind NGS Sequencer FASTASeq 300

mNGS / tNGS / Panel / NIPT / PGT-A  / 16s / forensic / eDNA


Learn More about FASTASeq 300

SURFSeq​ 5000 
Flexible Benchtop High-Throughput NGS Platform

HIGH Throughput

50 Gb to 2.2 Tb

​Genemind NGS Sequencer SURFSeq 5000

WES / WGS / cancer panel / Single cell sequencing / Spatial Transcriptomics
Learn More about SURFSeq 5000

SURFSeq​ Q 
Powerful bench-top high-throughput sequencing platform

ULTRA-HIGH Throughput

0.6 Tb to 14 Tb

Genemind NGS Sequencer SURFSeq Q

WES / WGS / cancer panel / Single cell sequencing / Spatial Transcriptomics
Learn More about SURFSeq Q

NGS Applications Supported by GeneMind Sequencers


Next Generation Sequencing is widely applied across research, clinical, agricultural, and industrial sectors.


Research Applications


  • Whole Genome Sequencing (WGS)
  • Whole Exome Sequencing (WES)
  • Single-cell sequencing
  • Epigenomics
  • Metagenomics


Clinical & Translational Applications


  • Oncology and tumor profiling
  • Rare disease diagnostics
  • Hereditary disorder screening
  • Targeted gene panels
  • Non-Invasive Prenatal Testing (NIPT)
  • Pharmacogenomics


Beyond Human Health


  • Microbiology and infectious disease surveillance
  • Public health monitoring
  • Environmental testing and food safety
  • Plant and animal breeding
  • Industrial biotechnology


The ability to rapidly generate and analyze complex sequencing data makes GeneMind platforms a strategic tool for accelerating discovery, improving diagnostics, and advancing innovation across life sciences.


NGS cancer panels from GeneMind

Cancer panels

Learn more

NGS Whole Genome Sequencing illustration

WGS

Learn more

NGS NIPT - Non Invasive prenatal testing

NIPT

Learn more

NGS Whole Exome Sequencing illustration

WES

Learn more

NGS Single-Cell Sequencing

Single-Cell Sequencing

Learn more

Contact us today to learn more about how GeneMind sequencers and their applications can revolutionize your NGS activities.
Contact us

Cancer Panel NGS Solutions for Precision Oncology

Comprehensive Cancer NGS Panels – From 30 to 580 Genes


GeneMind offers a structured portfolio of cancer-focused NGS panels designed to support precision oncology in both routine clinical diagnostics and advanced genomic profiling.


These scalable panels provide flexibility according to clinical needs, testing volume, reimbursement frameworks, and the growing demands of personalized medicine.


30-Gene Breast & Lung Cancer Panel

Focused on key clinically actionable genes commonly used in treatment selection and guideline-based testing.

Ideal for routine molecular diagnostics in breast and lung cancer management.


130-Gene Core Pan-Cancer Panel

Broader mutation coverage across multiple tumor types.

Supports comprehensive, yet cost-effective molecular profiling for informed clinical decision-making.


580-Gene Comprehensive Pan-Cancer Panel

Designed for complex oncology cases and translational research.

Enables in-depth molecular characterization, biomarker discovery, and advanced therapy stratification.


  • Flexible Solutions for Modern Oncology Workflows
  • Scalable gene coverage from targeted to comprehensive profiling
  • Alignment with evolving precision medicine strategies
  • Support for routine diagnostics and translational research
  • Integration into established clinical NGS workflows


GeneMind cancer panels empower laboratories to deliver accurate genomic insights that support optimized patient care.



Genemind Application Note : Lung & Colon Cancer Solution

Genemind Application Note : Lung & Colon Cancer Solution

Download application note

Genemind Application Note : Core Pan-cancer Solution

Genemind Application Note : Core Pan-cancer Solution

Download application note

Genemind Application Note : Comprehensive Pan-cancer Solution

Genemind Application Note : Comprehensive Pan-cancer Solution

Download application note

Ready to Evaluate our Cancer Panels application?

Contact us today to learn how GeneMind can strengthen your oncology NGS applications.

Contact us

Whole Genome Sequencing (WGS) Solutions


GeneMind’s WGS solutions enable comprehensive genome-wide analysis for research and clinical applications.


From detecting rare genetic variants and investigating complex diseases to supporting precision medicine and agricultural genomics, GeneMind transforms raw sequencing data into clinically and scientifically relevant insights.


Key Advantages:


  • End-to-end workflow from sample to report
  • Scalable throughput for research and clinical environments
  • High accuracy and robust QC standards
  • Integrated bioinformatics pipeline
  • Application-focused analysis tools



Whole-Genome Sequencing (WGS) NGS Workflow in Lab

Application Note Available:

Includes workflow design, sequencing technology overview, bioinformatics pipeline, QC standards, and reporting tools.

Request the complete WGS application note.

Non-Invasive Prenatal Testing (NIPT) Solutions

Genemind Application Note : NIPT Solutions

Rapid and Reliable Prenatal Screening


GeneMind NIGM enables fast and accurate NIPT analysis from a single 10 mL maternal blood sample, starting as early as 9 weeks of gestation.


  • Results within 24 hours
  • 99% sensitivity
  • Automated analysis pipeline
  • Flexible workflows compatible with multiple sequencing platforms


Combining simplicity, scalability, and reliability, GeneMind NIPT supports confident prenatal screening in modern diagnostic laboratories.


Application Note Available:

Covers workflow, sequencing platforms, bioinformatics analysis, QC standards, and automated reporting.


Request the complete NIPT application note.

Whole Exome Sequencing (WES) Solutions

Focused Genomic Insights for Hereditary Disease Research


GeneMind’s WES solution targets protein-coding regions to support clinical research in hereditary disorders.


Coverage Includes:

  • SNVs
  • Indels
  • CNVs
  • Mitochondrial DNA variants


The platform covers nearly all pathogenic and likely pathogenic variants listed in ClinVar and LOVD databases. A SNP-based framework ensures reliable CNV detection.


Key Features:


  • Automated library preparation
  • Target enrichment workflow
  • Integrated annotation and filtering tools
  • Web-based interpretation platform
  • Gender QC, sample tracking, cross-contamination monitoring


GeneMind WES transforms complex genomic datasets into actionable diagnostic insights.


Application Note Available:

Includes workflow, enrichment strategy, sequencing platforms, bioinformatics pipeline, and QC standards.

Ask for complete WES application note

Genemind Application Note : NGS Solutions for WES

Single-Cell Sequencing Solutions

Genemind Application Note : Single-Cell Sequencing NGS solutions


High-Throughput, Droplet-Based Microfluidics


GeneMind’s single-cell NGS platform leverages advanced droplet microfluidics to analyze thousands of individual cells using barcoded beads within nanoliter droplets.


Applications:


  • Tumor microenvironment studies
  • Immune cell profiling
  • Neural development research
  • Disease mechanism exploration
  • Rare cell identification
  • Differentiation trajectory tracking


Advantages:


  • High capture efficiency
  • Exceptional sensitivity
  • Integrated automated workflow
  • Cost-efficient large-scale analysis
  • Multi-omics compatibility


This solution accelerates discoveries in precision medicine and translational research.


Application Note Available:

Details transcriptomics, immune profiling, epigenetics, microbial RNA-seq, bioinformatics tools, and QC standards.


Request the complete Single-Cell application note.

Need Expert Guidance?


Our team is ready to support you in selecting the right NGS solution tailored to your research or clinical objectives.

Contact us

Our products

FASTASeq S Dx Sequencing System Set
GENEMIND BIOSCIENCES

FASTASeq S Dx Sequencing System Set

Reference : GENE-SQ00078
FASTASeq S redefines rapid sequencing, delivering lightning-fast turnaround from library preparation to final data output. Achieve results in just 2 hours for SE50, 3 hours for SE100, and 6.8 hours for PE150, enabling same-day insights for time-critical applications.

Powered by an ultra-high-speed fluidics architecture and an advanced enzymatic reaction system, FASTASeq S dramatically accelerates sequencing speed without compromising data quality. Its AI-driven base-calling engine enhances signal interpretation, ensuring exceptional accuracy even during high-speed runs.

With an optimized flow cell surface amplification design, the system produces robust, high-fidelity data—even from nanogram-level input samples. FASTASeq S empowers users to generate reliable sequencing results faster than ever before.
FASTASeq 300 Dx Sequencing System Set
GENEMIND BIOSCIENCES

FASTASeq 300 Dx Sequencing System Set

Reference : GENE-SQ00021
FASTASeq 300 is a powerful desktop high-throughput sequencing platform designed to deliver fast, reliable results for targeted sequencing and whole-genome low-pass applications. Built with next-generation sequencing chemistry, a high-density flow cell, advanced fluidics, and intelligent base-calling algorithms, it provides outstanding accuracy across every run.

These innovations offer users greater flexibility, highly consistent data quality, and significantly shorter turnaround times. Whether you're accelerating panel-based research, screening large sample cohorts, or generating rapid genomic insights, FASTASeq 300 empowers your team with a robust, efficient, and user-friendly sequencing solution.
SURFSeq 5000 Dx Sequencing System Set
GENEMIND BIOSCIENCES

SURFSeq 5000 Dx Sequencing System Set

Reference : GENE-SQ00026
SURFSeq 5000 is a powerful bench-top high-throughput sequencing platform designed to deliver speed, accuracy, and versatility across a wide range of genomic applications. With its fast run times, excellent data quality, and low startup cost, it enables laboratories to scale sequencing capacity without heavy infrastructure investment.

Engineered for maximum flexibility, SURFSeq 5000 supports whole-genome sequencing, targeted panels, transcriptomics, metagenomics, methylation sequencing, and more—making it an ideal all-in-one solution for diverse research and clinical workflows.

Whether you are driving scientific discovery or delivering high-confidence clinical results, SURFSeq 5000 empowers end-users with reliable performance, streamlined operation, and consistently high-quality data, all within a compact, user-friendly platform.
SURFSeq Q Dx Sequencing System Set
GENEMIND BIOSCIENCES

SURFSeq Q Dx Sequencing System Set

Reference : GENE-SQ00065
SURFSeq Q is an ultra-high-throughput sequencing platform designed to deliver unparalleled daily data output for large-scale genomics projects. By combining high-speed chemistry, advanced patterned array flow cells, and AI-powered base recognition, SURFSeq Q consistently achieves Q40 scores ≥90%, producing up to 9 Tb of data per day in a single run.

Its exceptional accuracy and productivity make it ideal for population-scale cohort studies, single-cell profiling, and spatial omics research, empowering scientific discovery and sequencing service providers with fast, reliable, and high-quality genomic data. SURFSeq Q transforms high-throughput sequencing into a streamlined, efficient, and scalable solution for modern laboratories.
Fragment Analyzer (Nanalyzer Dx)
GENEMIND BIOSCIENCES

Fragment Analyzer (Nanalyzer Dx)

Reference : GENE-M000048
The NanaLyzer Nucleic Acid Fragment Analyzer is an automated, high-precision system designed for fast and reliable DNA/RNA quality assessment. It supports flexible throughput from 1 to 96 samples using 8-strip tubes or 96-well plates, requiring only 2 μL per sample. Pre-cast microfluidic gel chips and isolated lanes ensure contamination-free, accurate fragment sizing and concentration measurement.

With automated loading, intelligent sample recognition, and rapid analysis—as fast as 15 minutes for 16 samples—NanaLyzer streamlines QC for NGS, molecular biology, and clinical research. Its compact design and easy-to-use software make it ideal for labs seeking speed, accuracy, and efficiency.
Automated Nucleic Acid Extractor (Genoscout EM Dx)
GENEMIND BIOSCIENCES

Automated Nucleic Acid Extractor (Genoscout EM Dx)

Reference : GENE-M000025
The GenoScout EM Automated Nucleic Acid Extractor delivers high-throughput, high-precision nucleic acid extraction with unmatched ease and reliability. Leveraging pre-packaged reagents with superparamagnetic silica-coated beads, it efficiently extracts and purifies nucleic acids from a wide range of biological samples—including blood, tissue, cells, body fluids, bacteria, and viruses. Using innovative magnetic bead technology, the system seamlessly performs nucleic acid adsorption, transfer, and release for efficient purification and enrichment. With its rapid, user-friendly operation and fully automated workflow, the GenoScout EM is the ideal solution for molecular diagnostics, animal disease detection, and other cutting-edge laboratory applications.
MrLH-96 Dx Automated Sample Preparation System
GENEMIND BIOSCIENCES

MrLH-96 Dx Automated Sample Preparation System

Reference : GENE-M000004
The MrLH-96 Automated Workstation revolutionizes high-throughput nucleic acid extraction, NGS library preparation, and laboratory liquid handling with seamless efficiency. Its intelligently designed consumable stacking system enables fully automated operation with minimal on-site manpower, saving time and reducing human error. Equipped with Inheco temperature-controlled oscillation accessories, it ensures precise and stable oscillation with temperature accuracy from 4°C to 70°C, perfectly tailored for NGS hybridization capture workflows. Additionally, the flexible script design system empowers users to customize workflows and explore multiple applications, making the MrLH-96 an indispensable tool for modern laboratories aiming for speed, precision, and versatility.
Designed to support diagnostic and research NGS workflows.
FASTASeq S Dx Sequencing System Set
GENEMIND BIOSCIENCES
FASTASeq S Dx Sequencing System Set
Reference : GENE-SQ00078
FASTASeq S redefines rapid sequencing, delivering lightning-fast turnaround from library preparation to final data output. Achieve results in just 2 hours for SE50, 3 hours for SE100, and 6.8 hours for PE150, enabling same-day insights for time-critical applications.

Powered by an ultra-high-speed fluidics architecture and an advanced enzymatic reaction system, FASTASeq S dramatically accelerates sequencing speed without compromising data quality. Its AI-driven base-calling engine enhances signal interpretation, ensuring exceptional accuracy even during high-speed runs.

With an optimized flow cell surface amplification design, the system produces robust, high-fidelity data—even from nanogram-level input samples. FASTASeq S empowers users to generate reliable sequencing results faster than ever before.
FASTASeq 300 Dx Sequencing System Set
GENEMIND BIOSCIENCES
FASTASeq 300 Dx Sequencing System Set
Reference : GENE-SQ00021
FASTASeq 300 is a powerful desktop high-throughput sequencing platform designed to deliver fast, reliable results for targeted sequencing and whole-genome low-pass applications. Built with next-generation sequencing chemistry, a high-density flow cell, advanced fluidics, and intelligent base-calling algorithms, it provides outstanding accuracy across every run.

These innovations offer users greater flexibility, highly consistent data quality, and significantly shorter turnaround times. Whether you're accelerating panel-based research, screening large sample cohorts, or generating rapid genomic insights, FASTASeq 300 empowers your team with a robust, efficient, and user-friendly sequencing solution.
SURFSeq 5000 Dx Sequencing System Set
GENEMIND BIOSCIENCES
SURFSeq 5000 Dx Sequencing System Set
Reference : GENE-SQ00026
SURFSeq 5000 is a powerful bench-top high-throughput sequencing platform designed to deliver speed, accuracy, and versatility across a wide range of genomic applications. With its fast run times, excellent data quality, and low startup cost, it enables laboratories to scale sequencing capacity without heavy infrastructure investment.

Engineered for maximum flexibility, SURFSeq 5000 supports whole-genome sequencing, targeted panels, transcriptomics, metagenomics, methylation sequencing, and more—making it an ideal all-in-one solution for diverse research and clinical workflows.

Whether you are driving scientific discovery or delivering high-confidence clinical results, SURFSeq 5000 empowers end-users with reliable performance, streamlined operation, and consistently high-quality data, all within a compact, user-friendly platform.
SURFSeq Q Dx Sequencing System Set
GENEMIND BIOSCIENCES
SURFSeq Q Dx Sequencing System Set
Reference : GENE-SQ00065
SURFSeq Q is an ultra-high-throughput sequencing platform designed to deliver unparalleled daily data output for large-scale genomics projects. By combining high-speed chemistry, advanced patterned array flow cells, and AI-powered base recognition, SURFSeq Q consistently achieves Q40 scores ≥90%, producing up to 9 Tb of data per day in a single run.

Its exceptional accuracy and productivity make it ideal for population-scale cohort studies, single-cell profiling, and spatial omics research, empowering scientific discovery and sequencing service providers with fast, reliable, and high-quality genomic data. SURFSeq Q transforms high-throughput sequencing into a streamlined, efficient, and scalable solution for modern laboratories.
Fragment Analyzer (Nanalyzer Dx)
GENEMIND BIOSCIENCES
Fragment Analyzer (Nanalyzer Dx)
Reference : GENE-M000048
The NanaLyzer Nucleic Acid Fragment Analyzer is an automated, high-precision system designed for fast and reliable DNA/RNA quality assessment. It supports flexible throughput from 1 to 96 samples using 8-strip tubes or 96-well plates, requiring only 2 μL per sample. Pre-cast microfluidic gel chips and isolated lanes ensure contamination-free, accurate fragment sizing and concentration measurement.

With automated loading, intelligent sample recognition, and rapid analysis—as fast as 15 minutes for 16 samples—NanaLyzer streamlines QC for NGS, molecular biology, and clinical research. Its compact design and easy-to-use software make it ideal for labs seeking speed, accuracy, and efficiency.
Automated Nucleic Acid Extractor (Genoscout EM Dx)
GENEMIND BIOSCIENCES
Automated Nucleic Acid Extractor (Genoscout EM Dx)
Reference : GENE-M000025
The GenoScout EM Automated Nucleic Acid Extractor delivers high-throughput, high-precision nucleic acid extraction with unmatched ease and reliability. Leveraging pre-packaged reagents with superparamagnetic silica-coated beads, it efficiently extracts and purifies nucleic acids from a wide range of biological samples—including blood, tissue, cells, body fluids, bacteria, and viruses. Using innovative magnetic bead technology, the system seamlessly performs nucleic acid adsorption, transfer, and release for efficient purification and enrichment. With its rapid, user-friendly operation and fully automated workflow, the GenoScout EM is the ideal solution for molecular diagnostics, animal disease detection, and other cutting-edge laboratory applications.
MrLH-96 Dx Automated Sample Preparation System
GENEMIND BIOSCIENCES
MrLH-96 Dx Automated Sample Preparation System
Reference : GENE-M000004
The MrLH-96 Automated Workstation revolutionizes high-throughput nucleic acid extraction, NGS library preparation, and laboratory liquid handling with seamless efficiency. Its intelligently designed consumable stacking system enables fully automated operation with minimal on-site manpower, saving time and reducing human error. Equipped with Inheco temperature-controlled oscillation accessories, it ensures precise and stable oscillation with temperature accuracy from 4°C to 70°C, perfectly tailored for NGS hybridization capture workflows. Additionally, the flexible script design system empowers users to customize workflows and explore multiple applications, making the MrLH-96 an indispensable tool for modern laboratories aiming for speed, precision, and versatility.
Designed to support diagnostic and research NGS workflows.

Related product categories

Nucleic acid extraction

DNA / RNA (Nucleic acids)

Nucleic acid extraction
Nucleic acid quality control

DNA / RNA (Nucleic acids)

Nucleic acid quality control
Nucleic acid amplification (PCR)

DNA / RNA (Nucleic acids)

Nucleic acid amplification (PCR)
Real-time PCR

DNA / RNA (Nucleic acids)

Real-time PCR
Sanger sequencing

DNA / RNA (Nucleic acids)

Sanger sequencing
NGS Library kits & Clean-up reagents

DNA / RNA (Nucleic acids)

NGS Library kits & Clean-up reagents
Automated NGS Library Preparation

DNA / RNA (Nucleic acids)

Automated NGS Library Preparation
Next Generation Sequencing (NGS)

DNA / RNA (Nucleic acids)

Next Generation Sequencing (NGS)
Nucleic acid decontamination

DNA / RNA (Nucleic acids)

Nucleic acid decontamination