Search Site Information
Search Site Information
Reads per Run
Up to 500 million reads per run
Samples
Supports up to 8 samples per run
Read Lengths
SE50, SE100, PE50, PE100, PE150
DNBSEQ-G50
The Desktop Sequencer that Packs a Punch
CE-IVD
RUO
DNBSEQ-G50 is a compact benchtop sequencer offering flexibility with two flow cells: FCS for rapid turnaround of STAT samples and FCL for cost-effective sequencing. It supports multiple read lengths and provides up to 150 GB per run, catering to various applications such as targeted, RNA, and whole genome sequencing.
Specifications
Explore the core capabilities and technical details.
Applications
Whole-Genome
Gene Expression
Targeted Analysis
Metagenomics
Identification
Methylation Analysis
Your Data Security is Our Top Priority
All our sequencing platforms can work as standalone systems from sample to result without any network connection, eliminating the risk of data breaches and ensuring complete data security.
The
DNBSEQ-G50
Advantage
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Reads per Run
Up to 500 million reads per run
Samples
Supports up to 8 samples per run
Read Lengths
SE50, SE100, PE50, PE100, PE150
DNBSEQ-G50
The Desktop Sequencer that Packs a Punch
CE-IVD
RUO
DNBSEQ-G50 is a compact benchtop sequencer offering flexibility with two flow cells: FCS for rapid turnaround of STAT samples and FCL for cost-effective sequencing. It supports multiple read lengths and provides up to 150 GB per run, catering to various applications such as targeted, RNA, and whole genome sequencing.
Specifications
Explore the core capabilities and technical details.
Applications
Whole-Genome
Gene Expression
Targeted Analysis
Metagenomics
Identification
Methylation Analysis
Your Data Security is Our Top Priority
All our sequencing platforms can work as standalone systems from sample to result without any network connection, eliminating the risk of data breaches and ensuring complete data security.
The
DNBSEQ-G50
Advantage
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Reads per Run
Up to 500 million reads per run
Samples
Supports up to 8 samples per run
Read Lengths
SE50, SE100, PE50, PE100, PE150
DNBSEQ-G50
The Desktop Sequencer that Packs a Punch
CE-IVD
RUO
DNBSEQ-G50 is a compact benchtop sequencer offering flexibility with two flow cells: FCS for rapid turnaround of STAT samples and FCL for cost-effective sequencing. It supports multiple read lengths and provides up to 150 GB per run, catering to various applications such as targeted, RNA, and whole genome sequencing.
Specifications
Explore the core capabilities and technical details.
Applications
Whole-Genome
Gene Expression
Targeted Analysis
Metagenomics
Identification
Methylation Analysis
Your Data Security is Our Top Priority
All our sequencing platforms can work as standalone systems from sample to result without any network connection, eliminating the risk of data breaches and ensuring complete data security.
The
DNBSEQ-G50
Advantage
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Dual Flow Cell Design
Flexible use of FCS for rapid STAT samples and FCL for cost-effective sequencing, catering to varied project needs.
Versatile Read Length Options
Offers 3-5 read length options, suitable for targeted sequencing to whole genome analysis.
Rapid Run Times and High Throughput
Run times from 9 to 40 hours, achieving up to 150 Gb per run, ideal for urgent research needs.
High-Quality Data Output
Over 80% Q30 score across read lengths, ensuring reliable and accurate results.
Dual Flow Cells for Flexibility & Multiple Read Length Options
Dual Flow Cells for Flexibility: DNBSEQ-G50 offers two flow cells: FCS for quick turnaround and STAT samples and FCL for cost-effective, larger-scale projects.
Multiple Read Length Options: Supports 3 to 5 read lengths, including SE100, SE50, PE100, and PE150, providing versatility for targeted sequencing, RNA sequencing, or whole-genome analysis.
High Throughput & Broad Range of Applications
High Throughput with Efficient Turnaround: DNBSEQ-G50 delivers 10 to 150 GB of data per run and supports PE150 sequencing in just 40 hours, making it ideal for research and clinical settings where rapid results are essential.
Broad Range of Applications: Supports targeted, low-pass, small whole genome, RNA, and whole exome sequencing, catering to diverse fields like clinical research, agriculture, and beyond.
Explore Applications
Metagenomics
Discover MGI's metagenomics NGS solutions for in-depth microbial analysis, from sample processing to detailed reports, uncovering hidden pathogens with cutting-edge sequencing technologies.
HIV-1 NGS solution
MGI's NGS solution enables efficient HIV-1 genotyping and drug resistance monitoring with advanced sequencing techniques for precise results.
Tuberculosis Drug Resistance Profiling
Experience rapid MTB identification, drug resistance, and traceability through sequencing with MGI's advanced tuberculosis detection and analysis solutions.
Explore Applications
Metagenomics
Discover MGI's metagenomics NGS solutions for in-depth microbial analysis, from sample processing to detailed reports, uncovering hidden pathogens with cutting-edge sequencing technologies.
HIV-1 NGS solution
MGI's NGS solution enables efficient HIV-1 genotyping and drug resistance monitoring with advanced sequencing techniques for precise results.
Tuberculosis Drug Resistance Profiling
Experience rapid MTB identification, drug resistance, and traceability through sequencing with MGI's advanced tuberculosis detection and analysis solutions.
Explore Applications
Metagenomics
Discover MGI's metagenomics NGS solutions for in-depth microbial analysis, from sample processing to detailed reports, uncovering hidden pathogens with cutting-edge sequencing technologies.
HIV-1 NGS solution
MGI's NGS solution enables efficient HIV-1 genotyping and drug resistance monitoring with advanced sequencing techniques for precise results.
Tuberculosis Drug Resistance Profiling
Experience rapid MTB identification, drug resistance, and traceability through sequencing with MGI's advanced tuberculosis detection and analysis solutions.
Explore Applications
Metagenomics
Discover MGI's metagenomics NGS solutions for in-depth microbial analysis, from sample processing to detailed reports, uncovering hidden pathogens with cutting-edge sequencing technologies.
HIV-1 NGS solution
MGI's NGS solution enables efficient HIV-1 genotyping and drug resistance monitoring with advanced sequencing techniques for precise results.
Tuberculosis Drug Resistance Profiling
Experience rapid MTB identification, drug resistance, and traceability through sequencing with MGI's advanced tuberculosis detection and analysis solutions.
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Product Brochure & Manuals
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Resources
Product Brochure & Manuals
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Resources
Product Brochure & Manuals
Product Brochure
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Discover innovative solutions that optimize every step of your sequencing process. Ready to enhance your results?
Discover innovative solutions that opti
mize every step of your sequencing process. Ready to enhance your results?
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Not for use in diagnostic procedures (except as specifically noted).
Join our newsletter to stay up to date on features and releases.
I have read and understood MGI’s Privacy Policy, and I consent to the collection and processing of my personal data for handling, responding to my contact, receiving your newsletter as well as promotion and marketing activities.
*For Research Use Only
Not for use in diagnostic procedures (except as specifically noted).
Join our newsletter to stay up to date on features and releases.
I have read and understood MGI’s Privacy Policy, and I consent to the collection and processing of my personal data for handling, responding to my contact, receiving your newsletter as well as promotion and marketing activities.
*For Research Use Only
Not for use in diagnostic procedures (except as specifically noted).