DNBSEQ T7+

MGI T7+ 2025
T7+: Ultra-Fast, High-Throughput Sequencing Without Compromise

T7+ is an integrated ultra-high-throughput sequencing platform built for labs that demand speed, accuracy, and scale. Leveraging MGI’s DNBSEQ™ Technology and SM2.0 biochemistry, it delivers over 14Tb of high-quality sequencing data in 24 hours, making large-scale genomics projects—from population studies to clinical pipelines—both feasible and efficient. Its 7-in-1 modular design automates the entire workflow, reducing hands-on time and minimizing potential errors.

Beyond sheer performance, T7+ is engineered with clinical relevance in mind. Its capacity for up to 35,000 whole-genome sequences annually ensures that your lab can meet high-throughput demands without compromising turnaround times. This efficiency directly translates to faster research insights, improved diagnostic workflows, and smoother integration into daily lab operations, helping you focus on what matters most: accurate, actionable genomic data.

>14 Tb/24h ultra-fast sequencing

7-in-1 automation: prep to analysis

QUAD-Flow Cells: PE150 & PE100 simultaneous

Q40 >90% high-quality output

Ergonomic & modular design

Smart system with diagnostics & self-healing

Omni-smart hub guides workflows

Checkpoint resume for uninterrupted runs

Learn more about how each feature works as you scroll.

Watch How T7+ Works
Why It Matters?

Every hour matters when precision, speed, and reliability determine outcomes. T7+ addresses these challenges by combining ultra-high throughput, rapid turnaround, and intelligent automation, so you can focus on results rather than processes.

Ultra-Fast Sequencing

Ultra-Fast Sequencing:

The proprietary TDI camera and high-density flow cells deliver over 14 Tb of high-quality data in 24 hours, supporting up to 35,000 whole-genome sequences per year. Large-scale projects can now be completed without bottlenecks.

Seamless Automation

Seamless Automation:

The 7-in-1 workflow integrates DNB preparation, loading, sequencing, waste management, data analysis, and compression. This reduces hands-on time, minimizes errors, and produces ready-to-analyze FASTQ files with Q40 >90%.

Chris Wicky

Clinical Genomics Manager - ANZ & Country Manager - NZ

Get a complete overview of T7+ performance, throughput, workflow automation, and configuration options. For guidance on integrating T7+ into your operations, Decode Science can provide personalized support and local assistance.
Download T7 Plus Brochure

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    Omni Start Hub

    Smart & Intuitive Operation:

    Minimalist design, adjustable screen angles, and the Omni-smart hub guide operations with ease, making daily sequencing as simple as interacting with a smartphone.

    Data compression lossless

    Reliable Data Management:

    Built-in lossless data compression reduces storage and bandwidth needs by up to 5× without compromising accuracy. Intelligent checkpointing ensures sequencing resumes seamlessly after interruptions.

    Empower Multi-Omics

    Versatility for Multi-Omics:

    T7+ supports WGS, spatio-temporal omics, cell-omics, proteomics, epigenomics, transcriptomics, and more, making it adaptable to evolving research and operational needs.

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    FAQs
    What is a TDI Camera?

    A TDI (Time Delay and Integration) camera is a high-performance imaging system used in MGI’s T20×2 ultra-high throughput sequencer to capture fluorescence signals with exceptional sensitivity and speed. Unlike conventional cameras that take static images, a TDI camera continuously scans across the sequencing slide, synchronizing image acquisition with sample movement. This technique integrates multiple exposures of the same area over time, significantly boosting signal strength and reducing noise. In the T20*, the TDI line-scan cameras work alongside a liquid-immersion optical lens and a large field-of-view objective to capture more fluorescence data per unit time with higher resolution. The result is faster, more accurate base identification and greater sequencing throughput — a cornerstone technology enabling MGI’s record-breaking data generation efficiency.

    What is DNBSEQ Technology?

    DNBSEQ is MGI’s proprietary sequencing platform based on DNA Nanoball (DNB) technology. Instead of traditional bridge amplification used by other platforms, DNBSEQ amplifies DNA fragments through rolling circle replication, creating dense, uniform DNA nanoballs that are then arrayed on a patterned flow cell. This approach eliminates amplification errors, reduces duplication rates, and enhances signal precision. Combined with MGI’s two-color fluorescence detection and advanced imaging systems, DNBSEQ delivers high-throughput, low-cost, and highly accurate sequencing results. The platform supports a wide range of applications—from whole genome and single-cell sequencing to metagenomics and oncology research—while offering superior data consistency and scalability compared to conventional NGS systems.

    What is SM 2.0?

    Standard MPS 2.0 (SM 2.0) is MGI’s next-generation sequencing chemistry designed to significantly enhance the accuracy and performance of its DNBSEQ™ platforms. By refining enzyme systems, optimizing fluorescent dyes, and improving data interpretation algorithms, SM 2.0 delivers exceptional sequencing quality—achieving over 85% of bases at Q40, or 99.99% base-calling accuracy. These advancements reduce noise, improve signal clarity, and minimize bias from upstream preparation. As a result, researchers gain higher confidence in detecting low-frequency mutations, SNPs, and InDels across applications such as whole genome sequencing, single-cell studies, and microbiome analysis. In essence, SM 2.0 sets a new industry standard for precision, reliability, and data quality in high-throughput sequencing.

    What happens if there’s a power outage or system interruption during a run?

    T7+ features checkpoint resume technology and proactive fault detection, allowing sequencing to continue without data loss once power or system issues are resolved.

    How much hands-on time is required per sequencing run?

    The 7-in-1 integrated workflow minimizes manual intervention—preparation and monitoring are streamlined, so staff can focus on data analysis rather than instrument operation.

    Can T7+ handle varying sample volumes or project scales?

    Yes. The modular QUAD-Flow Cell system allows independent runs, supporting both small batches and large-scale sequencing without compromising speed or accuracy.

    How easy is it to integrate T7+ into an existing lab workflow?

    The platform is designed to fit seamlessly into existing operations, with smart guidance, automated data processing, and flexible output formats that simplify downstream analysis.

    Ready To Order?
    As the authorised distributor for MGI in Australia and New Zealand, Decode Science makes adopting the T7+ effortless. We connect your lab with MGI’s ultra-high-throughput sequencing technology, helping you implement T7+ for faster, more reliable genomic results—with local support and guidance whenever you need it.
    MGI Portfolio

    DNBSEQ-T1+

    Accelerate high-throughput genomic testing with DNBSEQ-T1+

    The DNBSEQ-T1+ is one of the fastest T-level benchtop sequencers available globally—built on MGI’s proven DNBSEQ™ technology for accuracy, scalability, and reliability. Designed for clinical and translational genomics labs, the T1+ supports dual flow cell operation, delivering up to 1.2 terabases (Tb) of sequencing data within 24 hours (600 Gb per flow cell).

    For laboratories managing time-sensitive or high-volume projects, this means faster turnaround, improved workflow efficiency, and reduced dependence on external bioinformatics infrastructure. The optional integrated bioinformatics module enables automated secondary analysis immediately after sequencing, helping clinicians and molecular pathologists move from raw data to interpretable results without delay.

    In practice, DNBSEQ-T1+ helps streamline comprehensive genomic profiling (CGP), oncology testing, and clinical research pipelines—supporting both diagnostic accuracy and operational consistency across runs.

    High-Speed, High-Throughput Sequencing

    Generate up to 1.2 Tb of data in a single run with dual flow cell operation.

    Choose from FCL, FCM, or FCS flow cells to match your throughput needs—from small clinical batches to large oncology cohorts.

    Maintain >93% Q30 and >90% Q40 base quality across read lengths up to PE150.

    Complete full runs in as little as 7–24 hours, supporting faster reporting and clinical turnaround.

    Versatile Applications Across Clinical Genomics

    Flexible read lengths (SE50–PE300) suit NIPT, RNA-Seq, oncology panels, WES, WGS, and methylation studies.

    Supports coverage depth from 1 Gb to 120 Gb per sample, enabling both targeted assays and whole-genome workflows.

    Ideal for translational and precision medicine—from pathogen detection to tumour profiling.

    Integrated DNB Make & Load Technology

    DNB M&L (Make & Load) module automates DNB preparation and loading directly within the sequencer.

    Delivers consistent, contamination-free results with minimal hands-on time.

    Each flow cell operates independently, supporting different read lengths or applications in parallel.

    Enables an end-to-end “Make–Sequence–Analyse” workflow that saves time and reduces error.

    Smart Configurations and Automated Analysis

    Available in two setups: DNBSEQ-T1+ RS (flexible throughput) and T1+ ARS (with built-in bioinformatics).

    The ARS configuration automatically triggers advanced data analysis post-run, streamlining bioinformatics pipelines.

    Simplifies data interpretation for clinicians and molecular pathologists, improving workflow efficiency and diagnostic accuracy.

    Chris Wicky

    Clinical Genomics Manager - ANZ & Country Manager - NZ

    Download the DNBSEQ-T1+ brochure for a complete overview of performance metrics, application data, and configuration options. For guidance on how this platform fits your lab’s workflow, Decode Science can walk you through integration and local support options.
    Watch How T1+ Works
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    FAQs
    How can the DNBSEQ-T1+ support my existing oncology or CGP workflows?

    The T1+ integrates seamlessly into oncology and comprehensive genomic profiling (CGP) pipelines, providing the depth and coverage needed for both solid tumour and liquid biopsy applications. With PE150 read lengths and up to 1.2 Tb per run, it supports multi-sample batching without compromising turnaround time.

    What data quality can I expect for clinical reporting?

    Across all flow cell types, >93% of bases exceed Q30 and >90% exceed Q40, ensuring high-confidence variant detection for SNVs, indels, CNVs, and fusions. This level of consistency reduces the need for re-runs and strengthens the reliability of reported results.

    How fast can I expect sequencing results for patient samples?

    Depending on the mode, runs complete within 7–24 hours, with automated secondary analysis available immediately post-run on the T1+ ARS configuration. This supports faster clinical reporting and improved patient turnaround.

    Does the DNBSEQ-T1+ simplify lab workflows or require extra setup?

    The DNB Make & Load module automates DNB preparation within the sequencer, reducing manual steps, contamination risk, and hands-on time. Most labs can run end-to-end sequencing with minimal intervention after library prep.

    Can I run different assays on the same instrument?

    Yes. Each flow cell operates independently, allowing different read lengths or applications—for example, running oncology panels alongside RNA-Seq or WES on the same instrument without downtime.

    Ready To Order?
    As the authorised distributor for MGI in Australia and New Zealand, Decode Science makes adopting the DNBSEQ-T1+ effortless. We bridge your lab with MGI’s high-throughput sequencing technology, helping you implement the T1+ for faster, more reliable genomic insights—supported locally whenever you need it.
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    DNBSEQ-E25

    PRODUCTS

    DNBSEQ-E25

    DNBSEQ-E25 : Sequence Your Samples On-The-Go

    Embark on a streamlined sequencing journey from sample to report with the DNBSEQ-E25 sequencer. This compact and standalone system is designed to operate effortlessly inside or outside the lab, providing versatility in its usage. The E25 seamlessly integrates a microfluidic chip, an integrated CMOS detection module, self-luminous dye, and a proprietary computing module. This harmonious combination results in a lightweight and cost-effective instrument that breaks free from location restrictions, allowing you to conduct sequencing processes with ease and efficiency. The DNBSEQ-E25 is your solution for convenient and accessible sequencing wherever you need it.

    Plug-and-Play

    This integrated sequencer is ideal for remote sites, providing ease-of-use and convenience.

    Efficient

    Quick and easy setup means you can start your run in just 10 minutes.

    Hassle-free

    No washing between runs streamlines your sequencing.

    Plug-And-Play

    Experience seamless and hassle-free sequencing with our plug-and-play solution. The DNBSEQ-E25 incorporates an integrated microfluidic sequencing chip with a CMOS detection module underneath each spot. This innovative design minimizes environmental sensitivity, reduces costs, and lightens the weight of the sequencer. The result is a truly plug-and-play system, streamlining the sequencing process and providing you with an efficient and user-friendly solution for your research needs.

    E25 Features with DecodeScience
    Data Analysis Has Never Been Easier

    Simplify your data analysis process with the DNBSEQ-E25, where efficiency meets ease. The advanced model, DNBSEQ-E25A, takes it a step further by incorporating an enhanced computing module capable of running data analysis for various applications, including whole-genome sequencing. These sequencing platforms operate as standalone systems, managing the entire workflow from sample to result without the need for a network connection. This not only ensures ease of use but also eliminates the risk of data breaches, providing you with a secure and reliable solution for your sequencing needs.

    E25 Data
    Ready To Order?
    Our team can help you in placing the order. Click below to get a quote and fast ordering.
    MGI Portfolio

    Have a question?

    Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

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      DNBSEQ-G400

      PRODUCTS

      DNBSEQ-G400

      MGI G400
      DNBSEQ-G400 : Your Day-to-Day Sequencing Solution

      Elevate your day-to-day sequencing experience with the DNBSEQ-G400, your comprehensive sequencing solution. This system offers a versatile range of sequencing options, accommodating read lengths of up to SE400/PE300 and supporting two flow cell types. With built-in primary data analysis and optimized optical and biochemical systems, the DNBSEQ-G400 ensures a seamless and efficient sequencing process for your daily research needs. Trust in this innovative solution to deliver reliable and high-quality results, making it an essential tool for your routine sequencing endeavors.

      Accurate

      Our proprietary DNBSEQ technology ensures exceptional accuracy, eliminating clonal errors and index hopping-generating >99% SNP/indel precision and sensitivity.

      Versatile

      With a wide dynamic range (between 55 GB and 1440 GB per run per day) the G400 supports multiple read lengths, from SE50 up to SE400 or PE300.

      Flexible

      Choose between two flow cell types, depending on your throughput and runtime requirements. PE150 sequencing can be completed in as little as 37 hours.

      Features

      The sequencing platform offers a broad data output range of 55 Gb to 1440 Gb per run, with PE150(FCS) sequencing achieving full capacity in just 37 hours. It supports various read lengths, including SE50, SE100, SE400, PE100, PE150, PE200, and PE300. The platform’s versatility extends to diverse applications, encompassing basic research, clinical research, forensics, and agriculture, making it suitable for a wide range of scientific and investigative endeavors.

      DNBSEQ-G400
      Performance of G400 with DecodeScience
      Ready To Order?
      Our team can help you in placing the order. Click below to get a quote and fast ordering.
      MGI Portfolio

      Have a question?

      Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

        Or give us a call at:

        1300 581 991

        DNBSEQ-T7

        Turbocharge Your Sequencing with MGI DNBSEQ-T7

        High-throughput sequencing projects often stall when data volume, turnaround time, or workflow scalability become limiting factors — especially in whole genome, deep exome, transcriptome, and epigenome studies. Traditional platforms struggle to keep pace, leading to longer runtimes, bottlenecks between runs, and delayed analysis.

        DNBSEQ-T7 solves this by delivering ultra-high-throughput sequencing designed specifically for data-intensive genomics.
        Built on DNBSEQ™ Technology, it combines advanced biochemical, fluidic, and optical systems to generate up to 6 terabytes of high-quality sequencing data per day, enabling faster completion of large and parallel sequencing projects.

        Designed for population-scale studies and production sequencing, DNBSEQ-T7 allows labs to run multiple workflows simultaneously without compromising data quality or consistency. It fits seamlessly into large genomics programs where speed, scale, and sustained performance are critical.

        For genomics core facilities and research institutes running high-volume sequencing operations, DNBSEQ-T7 removes throughput constraints and accelerates time to results—without forcing workflow trade-offs.

        But... Why T7?

        Reads Per Run

        Up to 24 billion reads per run

        Samples

        Processes up to 60 whole human genomes per day

        Read Lengths

        PE100, PE150, App-A

        SPECIFICATIONS

        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.

        Dimensions & Weight

        1. Dimensions (L × W × H): 1656 mm × 903 mm × 1815 mm

        2. Net Weight: 765 kg

         

        Power

        1. Power Type: 200 V~240 V, 50/60 Hz, 30 A

        2. Rated Power: 3000 VA

         

        Floor Bearing Capacity

        Over 650 kg/m²

         

        Operational Environment Requirements

        1. Temperature: 19°C~25°C; fluctuation < 2°C per hour

        2. Relative Humidity: 30% RH ~ 80% RH; non-condensing

        3. Atmospheric Pressure: 80 kPa ~ 106 kPa

        4. Waterproof Rating: IPX0

        5. Altitude: Below 2000 meters

         

        Bandwidth for Network Connection

        300 Mb/s: For local storage network uploads

        Number of Flow Cells : 1-4

        Reads : 5800 M

        Read Length

        1. PE100:

          1. Data Output: 1 – 4 Tb

          2. Run Time: 20 – 22 hr

          3. Q30: >85%

        2. PE150:

          1. Data Output: 1.5 – 6 Tb

          2. Run Time: 24 – 30 hr

          3. Q30: >85%

        The maximum number of effective reads is based on the sequencing of an internal standard library. Actual output may vary with sample types and library preparation methods.

        Run time includes DNB loading, sequencing, and base calling. The percentage of base above Q30 is the average of an internal standard library over the entire run. The actual performance is affected by factors such as sample type, library quality, and insert fragment length.

        The DNBSEQ sequencing platforms are for Research Use Only. Not for use in diagnostic procedures.

        DNBSEQ-T7 (CE-IVD)

        Product Code: 900-000241-00

         
        DNBSEQ-T7RS

        Product Code: 900-000242-00

        Ebru Boslem

        ANZ Market Manager - Research Genomics

        For guidance on integrating T7 into your research, Decode Science can provide personalised support and local assistance. Simply reach out to me.
        MGI Portfolio

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          DNBSEQ-G99

          PRODUCTS

          DNBSEQ-G99

          G99 with DecodeScience
          DNBSEQ-G99 : The Ultimate in Sequencing Speed

          Introducing the DNBSEQ-G99, the epitome of sequencing speed and efficiency. This groundbreaking sequencer stands as the fastest ever created, offering unparalleled performance in low- to mid-range throughput, making it an exceptional choice for targeted gene and small genome sequencing research. The G99 features a triangular configuration on the patterned array, achieving a higher density of DNA Nanoballs (DNBs) and consequently yielding an impressive data output of up to 48 gigabytes per run.

          Equipped with a proprietary high-resolution objective lens and a high-precision temperature control system, the DNBSEQ-G99 sets a new standard for efficiency. With a remarkable run time for PE150 sequencing, completing the process within just 12 hours, this sequencer ensures swift and reliable results. Notably, during PE100 or PE150 sequencing runs, informative preliminary reports are available within the first 2.5 hours, providing researchers with rapid insights into their experiments. The DNBSEQ-G99 redefines sequencing capabilities, offering researchers an unprecedented combination of speed, density, and data output for accelerated and informative sequencing workflows.

          Fast

          Get up to 48 Gb (PE150 sequencing) in less than 12 hours.

          Flexible

          Run two independent flow cells at any time.

          Easy-to-Use

          Pre-loaded cartridges minimize human errors.

          Dual Flow Cells for Maximum Flexibility

          The DNBSEQ-G99 introduces a remarkable feature—dual flow cells for maximum flexibility. This innovative capability allows the sequencer to run two flow cells independently, providing users with the adaptable option to plug-and-play as needed. This dual-flow cell design enhances versatility and enables researchers to tailor their sequencing experiments to specific requirements, further expanding the utility and flexibility of the DNBSEQ-G99 in various applications.

          Dual Flow Cells for Maximum Flexibility G99
          Get up to 48 Gb per sequencing run

          Unlock unparalleled sequencing capabilities with the DNBSEQ-G99 and achieve up to 48 gigabytes of data per sequencing run. This impressive data output sets a new standard in sequencing efficiency, providing researchers with extensive genomic information in a single run. The DNBSEQ-G99 empowers users to generate large volumes of high-quality data, enabling comprehensive insights and accelerating advancements in genomics research.

          Performance of G99 with DecodeScience
          Ready To Order?
          Our team can help you in placing the order. Click below to get a quote and fast ordering.
          MGI Portfolio

          Have a question?

          Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

            Or give us a call at:

            1300 581 991