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DNBSEQ-G400
Your Day-to-Day Sequencing Solution
Step into a world where precision, storage, and versatility reign supreme with DNBSEQ-G400, a versatile benchtop sequencer that provides users with accurate, flexible, and efficient sequencing options. This production-scale sequencer will support your applications in a wide range of research topics with a capability to produce up to 1080 Gb output data in a single run with multiple read length options. Based on MGI's proprietary DNBSEQ™ Technology technology, DNBSEQ-G400 supports multi-sequencing modes with increased accuracy, decreased duplicates and reduced index hopping.
Redefine your research boundaries and strengthen your daily sequencing capability in medical and scientific research fields.
The
DNBSEQ-G400
Advantage
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
DNBSEQ-G400
Your Day-to-Day Sequencing Solution
Step into a world where precision, storage, and versatility reign supreme with DNBSEQ-G400, a versatile benchtop sequencer that provides users with accurate, flexible, and efficient sequencing options. This production-scale sequencer will support your applications in a wide range of research topics with a capability to produce up to 1080 Gb output data in a single run with multiple read length options. Based on MGI's proprietary DNBSEQ™ Technology technology, DNBSEQ-G400 supports multi-sequencing modes with increased accuracy, decreased duplicates and reduced index hopping.
Redefine your research boundaries and strengthen your daily sequencing capability in medical and scientific research fields.
The
DNBSEQ-G400
Advantage
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
DNBSEQ-G400
Your Day-to-Day Sequencing Solution
Step into a world where precision, storage, and versatility reign supreme with DNBSEQ-G400, a versatile benchtop sequencer that provides users with accurate, flexible, and efficient sequencing options. This production-scale sequencer will support your applications in a wide range of research topics with a capability to produce up to 1080 Gb output data in a single run with multiple read length options. Based on MGI's proprietary DNBSEQ™ Technology technology, DNBSEQ-G400 supports multi-sequencing modes with increased accuracy, decreased duplicates and reduced index hopping.
Redefine your research boundaries and strengthen your daily sequencing capability in medical and scientific research fields.
The
DNBSEQ-G400
Advantage
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
DNBSEQ-G400
Your Day-to-Day Sequencing Solution
Step into a world where precision, storage, and versatility reign supreme with DNBSEQ-G400, a versatile benchtop sequencer that provides users with accurate, flexible, and efficient sequencing options. This production-scale sequencer will support your applications in a wide range of research topics with a capability to produce up to 1080 Gb output data in a single run with multiple read length options. Based on MGI's proprietary DNBSEQ™ Technology technology, DNBSEQ-G400 supports multi-sequencing modes with increased accuracy, decreased duplicates and reduced index hopping.
Redefine your research boundaries and strengthen your daily sequencing capability in medical and scientific research fields.
The
DNBSEQ-G400
Advantage
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
High Performance and Short Sequencing run time
Extremely low PCR amplification error accumulation, low amplification bias and low index hopping with DNBSEQ technology together with the ability to complete an FCS SE100 run from DNB to FASTQ in only 13 hours.
Versatile and Flexible Throughput
Supports dual flow cell system capable of running two flow cells and types (FCL and FCS) simultaneously covering 550M – 3600M reads/run, allowing up to 1440 Gb data output per run.
Support wide range of applications
Designed for a wide range of applications including scientific research, clinical research, disease prevention, environmental studies, agriculture etc. and supports medium to large genome sequencing projects, capable of generating up to 1.4 billion reads per run.
Cost-Effective and User-Friendly
Offers a cost-effective solution with a user-friendly interface, enabling efficient operation and reducing total sequencing cost by up to 30%.
Specifications
Explore the core capabilities and technical details.
Instrument Specifications
Instrument Specifications
Instrument Specifications
Performance parameters
Performance parameters
Performance parameters
Resources
Sequencing Applications
DNBSEQ-E25
Popular Applications & Methods
Key Application
Large Whole-Genome Sequencing (human, plant, animal)
Metagenomics for pathogen detection Small WGS
Exome & Large Panel Sequencing (enrichment-based)
Targeted Gene Sequencing
(amplicon- based, gene panel)
Stereo-Seq and Single-Cell Profiling
Transcriptome Sequencing (total RNA-Seq, mRNA-Seq, gene expression profiling)
Profiling DNA Methylation
Forensic identification
DNBSEQ-G99
Popular Applications & Methods
Key Application
Large Whole-Genome Sequencing (human, plant, animal)
Metagenomics for pathogen detection Small WGS
Exome & Large Panel Sequencing (enrichment-based)
Targeted Gene Sequencing
(amplicon- based, gene panel)
Stereo-Seq and Single-Cell Profiling
Transcriptome Sequencing (total RNA-Seq, mRNA-Seq, gene expression profiling)
Profiling DNA Methylation
Forensic identification
DNBSEQ-G400
Popular Applications & Methods
Key Application
Large Whole-Genome Sequencing (human, plant, animal)
Metagenomics for pathogen detection Small WGS
Exome & Large Panel Sequencing (enrichment-based)
Targeted Gene Sequencing
(amplicon- based, gene panel)
Stereo-Seq and Single-Cell Profiling
Transcriptome Sequencing (total RNA-Seq, mRNA-Seq, gene expression profiling)
Profiling DNA Methylation
Forensic identification
DNBSEQ-T7
Popular Applications & Methods
Key Application
Large Whole-Genome Sequencing (human, plant, animal)
Metagenomics for pathogen detection Small WGS
Exome & Large Panel Sequencing (enrichment-based)
Targeted Gene Sequencing
(amplicon- based, gene panel)
Stereo-Seq and Single-Cell Profiling
Transcriptome Sequencing (total RNA-Seq, mRNA-Seq, gene expression profiling)
Profiling DNA Methylation
Forensic identification
Explore Applications
Explore Applications
Explore Applications
Explore Applications
Schedule a Meeting with Us
Discover the future of high-throughput sequencing. Schedule a consultation to explore the DNBSEQ-G400 for your research needs
Resources
Product Brochure & Manuals
Product Brochure
Resources
Product Brochure & Manuals
Product Brochure
Resources
Product Brochure & Manuals
Product Brochure
Frequently asked questions about DNBSEQ-G400
How many Flow Cell types does PE300 have?
How many Flow Cell types does PE300 have?
How many Flow Cell types does PE300 have?
What type of software does PE300 adapt to?
What type of software does PE300 adapt to?
What type of software does PE300 adapt to?
What is the maximum data output/of PE300?
What is the maximum data output/of PE300?
What is the maximum data output/of PE300?
What applications can PE300 do?
What applications can PE300 do?
What applications can PE300 do?
Whether pooling library
Whether pooling library
Whether pooling library
How many inserts are supported?
How many inserts are supported?
How many inserts are supported?
Can the Illumina PhiX Control v3 library be used as a balancing library?
Can the Illumina PhiX Control v3 library be used as a balancing library?
Can the Illumina PhiX Control v3 library be used as a balancing library?
Does it support custom read lengths?
Does it support custom read lengths?
Does it support custom read lengths?
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