DNBSEQ-T1+

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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.
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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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MGI Portfolio

DNBSEQ-E25

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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.

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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
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    DNBSEQ-G400

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    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.

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    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
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      DNBSEQ-T7

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      PRODUCTS

      DNBSEQ-T7

      DNBSEQ-T7 : Turbocharge your Sequencing

      Experience a sequencing revolution with the T7, designed to turbocharge efficiency across diverse projects such as whole genome, deep exome, epigenome, transcriptome, single-cell omics, spatial omics, and more. The T7 not only optimizes the entire sequencing process but also achieves extraordinary productivity. With the capability to generate a staggering 20,000 30x whole genomes in just one year, all at an affordable cost of $150 per genome, the T7 sets a new benchmark for high-quality data acquisition at an unparalleled speed. Embrace the future of genomics research with the T7, where efficiency meets affordability without compromising data quality.

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      Flexible

      The T7 offers unmatched flexibility with its 4 independent flow cells, empowering you to run them at any time without the need to batch large quantities of samples

      Fast

      Achieve 24/7 production with your large sequencing project by generating 7 Tb data in 24 hours with automatic washes in between runs

      Accessible

      The T7 opens the doors to accessibility for your groundbreaking sequencing projects

      Say Goodbye to Amplification Errors Associated with PCR

      Bid farewell to amplification errors linked with PCR, as our cutting-edge technologies ensure precise and error-free amplification processes. With our advanced solutions, we prioritize accuracy and reliability, ensuring that your results are free from the concerns associated with amplification errors. Embrace a new era in PCR technology where precision and confidence in your data are paramount.

      T7Inside Workflow
      Independent Flow Cells

      Experience unparalleled flexibility in your sequencing workflows with the inclusion of 4 independent flow cells in our technology. These independent flow cells grant you the freedom to run sequencing processes at any time, eliminating the necessity to batch large quantities of samples. This innovative design empowers you to adapt your sequencing runs to specific requirements, offering enhanced efficiency and customization in your research endeavors.

      T7 Quad Cells
      Performane of T7 with DecodeScience
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        DNBSEQ-G99

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        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.

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        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
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        Our team can help you in placing the order. Click below to get a quote and fast ordering.
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        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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          1300 581 991