Genomic sequencing has evolved from a decade-long, billion-dollar endeavor into an accessible, high-speed tool within the reach of laboratories worldwide. The volume of genetic data that can be generated has grown exponentially, unlocking new frontiers across precision medicine, agriculture, environmental conservation, and public health.
Yet for many researchers and clinicians, navigating the rapidly expanding landscape of sequencing technologies can be overwhelming. It is difficult to know which innovations are truly driving discovery and which are best suited to your specific research needs.
This eBook charts ten years of genomic innovation, tracing the milestones, technologies, and real-world breakthroughs that have shaped modern life science, providing the context and insight to make informed decisions about the tools you need.
Download this eBook to learn:
- How sequencing costs decreased from billions to under $100
- The key technological advances transforming genomics workflows
- Real-world case studies showing how accessible genomic tools are being applied worldwide
Leading Life Science Innovation
Contents
Foreword�������������������������������������������������������������������3
Enhanced Genomic Discovery: The MGI
Journey���������������������������������������������������������������������4
A New Era of Affordable Sequencing �������������������������13
The Visionaries Who Made Modern
Genomics Possible ��������������������������������������������������� 14
10 Defining Milestones in MGI’s
Genomics Journey ����������������������������������������������������15
Genomic Solutions Driving Innovation ������������������������ 22
Global Impact: MGI in Action ������������������������������������� 35
A Lifelong Journey of Genomic
Discovery: Reflecting on a Decade of
DNBSEQ Innovation and Beyond���������������������������������40
Resources����������������������������������������������������������������43
2Leading Life Science Innovation
Foreword
The story of genomics is one of humanity’s most ambitious scientific endeavors. What began as a decade-long, billiondollar international collaboration can now be accomplished a single day for less than $100. This transformation
represents more than technological progress; it marks a fundamental shift in how we understand biology, diagnose
disease, protect our environment, and feed our planet.
Since its founding in 2016, MGI has consistently driven the field of genomics forward. As the only company to master all
three key sequencing signal detection modes, delivering clinical-grade short and long read sequencers across the full
throughput spectrum, MGI has established itself as a key player in the global genomics landscape.
This eBook celebrates 10 years of innovation, growth, and global impact. It highlights the real-world applications of
accessible genomic technology, from protecting Thailand’s coastal ecosystems to expanding precision medicine access
across Latin America. It explores how the exponential growth in data generation is just the beginning of genomics’ next
phase. Most importantly, it demonstrates how MGI is committed to making sequencing accessible worldwide,
accelerating the pace of discovery, and collaborating to achieve the full potential that genomics offers.
Listen to Their Stories Over
the Past Decade
Watch Video
3Leading Life Science Innovation
Enhanced Genomic Discovery:
The MGI Journey
The story of genomics represents more than just technological progress; it marks a fundamental shift in how we
understand biology, diagnose disease, protect our environment, and feed our planet. The volume of genetic data that
can be generated has grown exponentially over the last decade, from kilobases using early pipette-based methods to
terabases using modern platforms such as spatiotemporal chips.
Genetic analysis that once cost billions of dollars and required over a decade of work can now be performed in hours for
under $100. This democratization of sequencing technology has unlocked population-scale studies and opened new
frontiers across precision medicine, agriculture, public health monitoring, and biodiversity conservation.
Since its founding in 2016, MGI has been a catalyst in transforming the genomic landscape. As one of the few companies
worldwide capable of independently developing and mass-producing clinical-grade gene sequencers across the full
throughput spectrum, MGI has grown to serve over 3,560 users across more than 110 countries and regions. This eBook
explores MGI’s journey of innovation and global expansion, highlighting the company’s strategic milestones that have
defined the last decade.
The evolution of genome sequencing
The path to today’s sequencing revolution began with Frederick Sanger’s chain-termination sequencing method in the
1970s. This development enabled scientists to read DNA sequences and laid the foundation for the Human Genome
Project, which became an international effort costing approximately $3 billion over the course of a decade.
The next major shift came in the mid-2000s with the advent of next-generation sequencing (NGS), which leverages
massively parallel sequencing (MPS) to analyze millions of DNA fragments simultaneously. This breakthrough reduced
both costs and timeframes, enabling the transition from single-genome projects to population-scale studies and
bringing genomics to thousands of laboratories worldwide.
In the current market, modern sequencing techniques
must balance a range of competing factors: throughput,
accuracy, read length, cost per sample, and ease of use.
Different applications demand different solutions, from
ultra-high-throughput platforms capable of sequencing
thousands of whole genomes for population studies, to
compact benchtop systems suited for clinical laboratories
performing targeted diagnostic panels. The field is
accelerating as innovations in library preparation,
automation, and data analysis make genomic information
more accessible and actionable.
Sequencing Challenges
Accuracy
Cost per
sample
Throughput
Ease of use
The different aspects of sequencing that need to be balanced.
4Leading Life Science Innovation
MGI enters the field
In 2016, we founded MGI with a clear mission: to develop and promote advanced life science tools for
future healthcare. But our vision went deeper than simply developing new instruments. We saw an
opportunity to democratize access to genomic technology worldwide.
We envisioned creating an independent company capable of developing and manufacturing clinicalgrade sequencers across the full spectrum of applications. What drove this vision was not merely a
commercial opportunity, but a conviction that genomic technology should be accessible to researchers,
clinicians, and communities everywhere.
From day one, MGI has innovated rapidly, responded to market needs, and expanded strategically and
globally. It is an exciting time in the field of genomics, and the next decade holds as much promise for
MGI as the last.
— Duncan Yu, President, MGI Tech Co., Ltd.
Product and technology innovation journey
The technological foundation for MGI’s vision began with
DNBSEQ™ (DNA Nanoball Sequencing). This proprietary
sequencing approach creates compact “nanoballs” of
DNA through rolling circle amplification, then sequences
them on precisely patterned array chips using
combinatorial probe-anchor synthesis (cPAS). This
approach delivers distinct advantages: exceptional
accuracy, low duplication rates, and minimal index
hopping compared to other sequencing methods,
characteristics that prove crucial for clinical applications.
Since BGISEQ-500 was launched and achieved costs
approaching $1,000 per genome, it has demonstrated that
accessible, high-quality sequencing was possible. MGI’s
journey toward commercialization began in 2016, when its
product portfolio expanded with the benchtop G400 and
G50 sequencers, serving laboratories with varying
throughput needs and establishing MGI’s ability to
manufacture clinical-grade instruments across
multiple scales.
BGISEQ-500 team building event.
5Leading Life Science Innovation
The 1,000th G99 gene sequencer rolls off the production line.
These early products laid the foundation for future
innovations, establishing MGI’s credibility as a serious
player in the global sequencing market. This was further
enhanced in 2017 when MGI achieved ISO 13485 Medical
Device Quality Management System certification, a crucial
milestone demonstrating adherence to the highest
international standards for medical devices.
In October 2019, MGI launched three new product series:
the DNBSEQ E series (including the world’s first selfluminescent sequencer), the DNBelab D series (microfluidic
library preparation systems), and the DNBelab C series
(single-cell analysis platforms). MGI’s portfolio also
expanded beyond sequencing with the US-R3 robotic
ultrasound system (first launched in 2017), which received
both China’s NMPA and EU regulatory approvals and
represented an entry into intelligent medical imaging.
Product innovation continued at a rapid pace, and in September 2023, MGI launched the DCS (DNA Omics, Cell Omics,
Spatial Omics) Lab Initiative. As of June 2025, 30 DCS labs were established globally, creating hubs for advanced research
and collaboration.
In February 2024, MGI introduced StandardMPS 2.0 sequencing reagents, which achieve Q40 sequencing quality—99.99%
base-calling accuracy—a significant benchmark in the industry that sets new standards for clinical-grade sequencing.
In September 2025, MGI formally organized its technology portfolio into three integrated business segments: SEQ ALL (a
complete sequencing platform portfolio), GLI (Generative Lab Intelligence, encompassing automation and AI-driven
laboratory solutions), and multi-omics (integrating single-cell analysis, spatial transcriptomics, and medical imaging).
In 2026, MGI acquired STOmics and CycloneSEQ, delivering integrated long-read, short-read, and spatial omics solutions.
This marks a significant milestone in MGI’s “SEQALL+GLI+Omics” strategy, positioning the company as the world’s only
manufacturer of core life science tools spanning short-read sequencing, long-read nanopore sequencing, generative lab
intelligence, and spatial omics technologies.
458+
International qualifications
and certifications in total
85+
Product categories
covered
90+
Countries and
regions covered
23
11
DNBSEQ™ sequencers have NMPA approval for clinical use,
accounting for nearly 60% of the total number of domestic
certificates obtained.
DNBSEQ™ sequencers support both DNA and RNA detection
for comprehensive applications like pathogen detection and
tumor RNA detection.
6Leading Life Science Innovation
Data Privacy and Security
MGI is committed to protecting your privacy. As a global enterprise, MGI takes all reasonable and legal
solutions to meet the requirements of privacy protection to comply with local laws and regulations.
Data Access
MGI is a supplier of the technology and products
for the customers. MGI does NOT provide any
gene-sequencing services. MGI does NOT own,
control, handle, or even access the genetic data,
but MGI’s customers do.
Security Safeguards
MGI’s sequencers are designed to be able to run
without connections to internet. Customers have
100% control of the data generated in the
instrument. Without connecting to the internet,
there is no risk from the internet of data access by
people outside the lab.
MGI’s sequencers are not equipped with any
wireless data transmission module. The Wired NIC
port is limited to build internal networks, such as
a laboratory information management system
(LIMS) connection. The USB port is used only for
emergency data backup to prevent data loss if a
customer’s intranet is under attack.
Privacy Protection Policy
MGI strictly abides by the principle of Privacy by
Design. MGI’s product design and configuration are
constructed through a comprehensive genetic data
security and protection system. MGI also provides
customers with specific suggestions on security
and protection in terms of physical and technical
environment for the equipment installation.
Third Party Certificates
MGI has acquired ISO 27001:2022 and
ISO 13485:2016 certificates, with ISO 27701:2019
certification in process. ZTRON Appliance has
been certified by European Privacy Seal
(EuroPriSe) in privacy protection.
Global expansion and customer experience journey
MGI was officially founded in Shenzhen, establishing its headquarters and first production base. In the same year, it
opened a production base in Wuhan, China.
In 2017, MGI opened its production base in Changchun, China, launching the manufacturing infrastructure that would
support global expansion. In 2019, a production facility was opened in Qingdao, China, to further expand manufacturing
capacity to meet growing demand.
The period from 2019 through 2021 marked MGI’s transformation from a promising startup to a global enterprise with
manufacturing and customer support infrastructure spanning multiple continents.
In November 2019, MGI opened an international production and logistics base in Riga, Latvia, providing a manufacturing
presence outside China.
7Leading Life Science Innovation
MGI achieves ISO13485 Medical Device Quality
Management System certification and
launches G400 and G50.
MGI is officially founded. MGI launches ultra-high-throughput
sequencer T7.
2016 2017 2018
2019 2021 2022 2023
MGI Latvia was established. MGI constructed an upgraded
manufacturing hub in Wuhan.
Reagent production line launched in Qingdao. MGI moved into new
headquarters in Shenzhen.
8Leading Life Science Innovation
2021 2022 2023 2024 2025
Australia Hong Kong Singapore
UK and Japan Germany and Brazil
MGI has spent half a decade opening Customer Experience
Centers, which provide researchers and clinicians with hands-on
technical support�
In 2020, the COVID-19 pandemic tested healthcare systems and diagnostic capabilities worldwide, demonstrating the
critical importance of accessible, reliable sequencing technology for global health security. As demand for the
technology grew, it became necessary to provide customers with hands-on access to technology, training, and local
support. This drove the development of Customer Experience Centers (CEC), facilities where researchers and clinicians
could experience training and ongoing technical support.
The first international CEC opened in Australia in 2021, followed by centers in the United Kingdom and Japan (both
2022), Hong Kong (2023), Germany and Brazil (both 2024), and Singapore (2025). Each CEC became a hub for local
scientific communities, hosting workshops, supporting collaborative research, and ensuring that MGI’s technology
integrated smoothly into diverse laboratory workflows.
9Leading Life Science Innovation
Recent innovations and market leadership
The years 2022 through 2025 marked MGI’s maturation as
a global enterprise and continued technological
leadership.
In September 2022, MGI went public on the Shanghai
Stock Exchange STAR Market (stock code: 688114.). The
same year brought another significant milestone when, in
July 2022, it was awarded $334 million in settlement of
intellectual property litigation.
In 2022, MGI also constructed an upgraded manufacturing
hub in Wuhan for products related to the life science and
biotechnology sectors, meeting world-class standards. In
2024, MGI unveiled European headquarters in Berlin,
Germany, further strengthening its infrastructure for
serving customers across continents.
On September 9th, 2022, MGI went public on the Shanghai Stock Exchange
with the stock code 688114.
By September 2025, MGI’s global workforce had grown to over 2,200 people, with approximately 27% dedicated to
research and development. More than 5,300 DNBSEQ and CycloneSEQ sequencing platforms have been sold worldwide,
and MGI’s service network continues to expand.
*Statistics as of 30 September, 2025
**Statistics as of 13 April, 2026
2,241
employees worldwide,
of which 27.04%*
are Research and
Development employees
1,132
valid patent applications
(cumulative)
3,560+
users in 100 countries/
regions worldwide
5,300+
DNBSEQ and
CycloneSEQ sequencing
platforms sold and
installed globally
18,000+
papers published in top
scientific journals**
10Leading Life Science Innovation
HQ in Shenzhen
Global impact and scientific contributions
At the close of December 2025, there were over 18,000 scientific articles published using DNBSEQ and CycloneSEQ
platforms. These publications span the biological spectrum, from population genomics and cancer research to
environmental monitoring and archaeology.
The applications extend far beyond human health. In agriculture, MGI technology supports crop breeding programs
worldwide, enabling researchers to develop more resilient, productive varieties suited to changing climate conditions.
This global impact hasn’t gone unrecognized, and MGI has received numerous prestigious awards, including a Green
World Award for sustainable contribution in 2025, a special mention in TIME Magazine’s Best Inventions of 2024, a Gold
Edison Award in 2024, and an R&D 100 Award in 2023.
MGI has also worked hard to establish strategic partnerships with leading research institutions, clinical laboratories, and
agricultural organizations worldwide. From Thailand’s National Omics Centre to the University of Lisbon, MGI’s
technology is enabling researchers and clinicians to address their communities’ most pressing challenges.
The global reach of MGI
San Jose, US
Boston, US
North America
London, UK
Stockholm, Sweden
Riga, Latvia
Berlin, Germany
Belgrade, Serbia
Europe
Dubai, UAE
Middle East
Brisbane, Australia
Oceania
Changchun
Beijing
Kunshan
Chengdu
Qingdao
Shanghai
Wuhan
Hong Kong
Singapore
Tokyo, Japan
Asia
São Paulo, Brazil
South America
Regional Office Comprehensive Base (Production/R&D/Marketing) Customer Experience Center (CEC)
11Leading Life Science Innovation
A decade of progress, decades of possibility ahead
MGI’s first decade has been marked by rapid evolution. Throughout this journey, MGI has remained committed to
making genomic technology accessible worldwide while maintaining the highest standards of quality and performance.
The following sections of this eBook provide detailed explorations of MGI’s key technologies, product lines, and application
areas. You’ll glimpse the future taking shape in MGI’s laboratories and partner institutions worldwide, and you’ll see how
MGI is building a future where intelligent systems accelerate discovery, where comprehensive multi-omics analysis reveals
biology’s full complexity, and where the tools of life science serve researchers and communities everywhere.
Discover how MGI’s innovations are transforming
life science research and clinical applications
aking reat nnovations
Discover A Decade of Making
Great Innovations.
Learn More
12A NEW ERA OF
AFFORDABLE SEQUENCING
In just over two decades, genome sequencing has transformed from a billion‑dollar
scientific moonshot into an accessible tool driving discovery worldwide.
Unlock the power of low-cost sequencing
References
1� Gunukula SR� Whole Genome Sequencing Cost 2023� 3billion� Published 29 December, 2022� Accessed 13 February, 2026� https://3billion�io/blog/whole-genomesequencing-cost-2023
2� Schwarze K, Buchanan J, Fermont JM, et al� The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United
Kingdom� Genetics in Medicine. 2020;22(1):85–94. doi: 10�1038/s41436-019-0618-7
2003
$3 billion1
• After 13 years of
hard work, the
Human Genome
Project completes
the human genome
sequence
• Next-generation
sequencing
emerges
• Costs begin rapid
decline
• The “$1,000
genome” barrier
broken
• Population-scale
studies become
feasible
• MGI launches T7
• High-throughput
platforms
accelerate cost
reduction
• Ultra-highthroughput systems
enable sub-$100
genomes and
produce up to
50,000 WGS per
year (T20×2)
• T7+ and T20×2
drive accessibility
2007
$1 million1
2014
$1,0001
2018
$6002
2025
<$100
Volume of Data
Cost
Terabases
KilobasesTHE VISIONARIES
WHO MADE MODERN
GENOMICS POSSIBLE
Every breakthrough in science stands on the foundation laid by those who came
before. The genomics revolution that MGI advances today was made possible by
decades of pioneering.
Mid-2000s:
The NGS Revolution
Early genomic research teams including
those of Radoje Drmanac, Jonathan
Rothberg, and David Klenerman
Next-generation sequencing technologies
enabled massively parallel sequencing,
analyzing millions of DNA fragments
simultaneously.
Costs plummeted from millions to thousands of
dollars. Sequencing time dropped from
years to days.
This opened the door for genomics to move
from research labs into clinical medicine and
population studies.
Discover the legacy of genomics
with the latest tools from MGI
1953: The Double Helix
James Watson, Francis Crick, and
Rosalind Franklin
The discovery of DNA’s double helix structure
revealed how genetic information is stored and
replicated.
For the first time, scientists could visualize the
molecule of heredity—establishing the
foundation for all subsequent molecular
biology research.
Understanding DNA’s structure made it possible
to imagine reading its sequence.
1990–2003: The Human
Genome Project
International Consortium of Researchers
The first complete human genome sequence
involved mapping 3 billion base pairs over 13
years at a cost of $3 billion.
This proved that genome sequencing was
possible and created the reference that all
future genomics would build upon.
It also demonstrated the need for faster, more
affordable sequencing technologies to make
genomics accessible.
2005–Present: Complete
Genomics and DNBSEQ™
Radoje Drmanac and the MGI Team
DNA Nanoball Sequencing (DNBSEQ™)
technology achieves unprecedented accuracy
through combinatorial probe-anchor synthesis
on patterned arrays.
High accuracy, low duplication rates, and
minimal index hopping enable clinical-grade
sequencing at scale. Costs continue to fall
toward the sub-$100 genome.
Genomics is becoming democratized, making
precision medicine, population health studies,
and agricultural genomics accessible across
continents.
From the double helix to DNA nanoballs, each
generation of scientists has pushed the
boundaries of what’s possible—building tools
that allow the next generation to see further.
Today, MGI carries this legacy forward,
developing technologies that bring the power of
genomics to researchers, clinicians, and
communities worldwide.
1977: Reading the Code
Frederick Sanger
The chain-termination sequencing method
enabled the first practical way to read DNA
sequences.
Sanger sequencing made it possible to
determine the exact order of DNA bases, earning
Sanger his second Nobel Prize.
This method powered the Human Genome
Project and remained the gold standard for
decades.Leading Life Science Innovation
10 Defining Milestones in
MGI’s Genomics Journey
Over the last decade, MGI’s journey has fundamentally shaped how genomic research is conducted and how healthcare
is delivered. By breaking down the barriers of high-throughput sequencing, MGI has turned cutting-edge technology into
an accessible reality for laboratories worldwide. Its journey has been defined by a series of transformative milestones—
from proprietary sequencing platforms to landmark studies—that have driven significant progress across the global
scientific community.
To mark this decade of progress, this listicle highlights 10 ways MGI has made lasting impacts on genomics research
and healthcare.
1� Driving high-speed results
at a fraction of the price
In 2017, MGI fundamentally changed the
cost–performance ratio in next-generation sequencing
with the launch of the G400 and G50. These sequencers
offer affordable, high-quality sequencing, with both
systems capable of completing a PE100 run in under 48
hours. By supporting four or more distinct read lengths,
they offer researchers flexibility across a broad range of
applications—from clinical diagnostics and forensics to
agriculture and environmental engineering. Launch of the G400 production line in Latvia.
15Leading Life Science Innovation
The G50 generates up to 60 gigabases (Gb) per run from a single flow cell and the G400 produces up to 600 Gb per run
across two flow cells. This 10-fold difference in throughput opens the door to rapid and reliable genomic insights for
laboratories at all scales.
2� Unleashing ultra-high-throughput power
High costs and slow turnarounds have long constrained
large-scale sequencing, until the launch of the T7 in 2018
shattered these constraints. Built for unprecedented
speed and throughput, the T7 produces up to 7 Tb of data
per day, transcending the daily production capacity of all
other platforms at the time. Its 24-hour turnaround for
PE150 runs has proven vital for rapid-response clinical
needs, spearheading critical viral characterization and
vaccine development efforts.
As demands grew for quick data handling on a large scale,
2025 saw the arrival of the T7+, an upgraded powerhouse
that packs accuracy and flexibility into a smaller footprint.
This instrument leverages four independent flow cells to
deliver over 14 Tb of ultra-high-quality sequencing data in
24 hours. Moreover, it integrates an intelligent 7-in-1
workflow from DNB preparation to analysis, allowing researchers to process 35,000 whole human genomes annually.
Today, these scalable sequencers remain the gold standard for high-speed, data-intensive research and clinical
applications.
3� Pioneering self-luminous sequencing
The launch of the E25 in 2022 changed the face of portable sequencing. As the world’s first sequencer to leverage selfluminous technology, the E25 eliminates the need for complex external excitation sources. Its compact and lightweight
design achieves unrivalled portability for on-the-go analyses, making sequencing accessible far beyond the confines of
traditional labs into airports, customs, and remote field locations.
Powered by a microfluidics-based flow cell with integrated complementary metal-oxide-semiconductor (CMOS)
modules, the E25 delivers FASTQ data from a DNA sample in just 20 hours. Its microfluidic chips remove the need for
washing between runs, further enhancing its ability to operate in settings without traditional infrastructure.
The T7+ launch.
16Leading Life Science Innovation
4� Setting a new pace
In 2022, MGI launched its ninth sequencer model, the G99,
one of the fastest mid- to low-throughput sequencers on
the market. It utilizes a first-of-its-kind triangular matrix
flow cell to achieve higher data density, delivering 8–48
Gb per run and completing PE150 runs in just 12 hours.
Crucially, MGI’s pursuit of speed doesn’t come at the cost
of quality: the G99 maintains a remarkably low error rate,
averaging 0.2%.
These capabilities make the G99 ideal for targeted and
small genome sequencing, particularly for precision
oncology and rapid tumor detection in hospitals. Its
real-world utility was proven during the discovery of the
first imported case of Monkeypox in Chongqing, China.
5� Breaking the sub-$100 genome barrier
For decades, the cost of whole genome sequencing (WGS)
remained a significant hurdle for large-scale research.
Even as prices dropped from millions in the mid-2000s to
around $600 by early 2023, the field was still far from
achieving true population-scale affordability. The launch
of T20×2 in 2023 redefined the economics of large-scale
sequencing, becoming the first platform to break the
sub-$100 genome barrier.
This record-breaking sequencer produces up to 50,000
whole genomes per year, with a massive 72 Tb output per
PE150 run, making it uniquely suited for large-population
genome projects. The low cost and high throughput of the
T20×2 are possible thanks to its unique ability to handle
six open-type large sequencing slides simultaneously. Its
innovative dip-immersion biochemistry and robotic
handling ensure uniform reactions across these large slides.
The G99 at the University of Lisbon, sequencing the Sahara dust storm.
The T20×2.
17Leading Life Science Innovation
6� Delivering full-spectrum sequencing
In 2024, the CycloneSEQ product line, including G100-ER and G400-ER, was introduced, equipped with nanopore
technology for real-time long-read sequencing. Powered by an innovative flow cell design and advanced base-calling
algorithms, the CycloneSEQ sequencers bridge the gap between long-read accuracy and high-throughput performance.
The G100-ER provides essential
flexibility across diverse sample
types and workflows in small- to
mid-scale projects. Meanwhile,
the G400-ER stands as the world’s
highest-throughput single-chip
nanopore sequencer. Designed
for high-output applications such
as whole-genome resequencing
and single-cell full-length
transcriptome studies, it
enhances both cycle time
and efficiency.
7� Transforming benchtop sequencing
Historically, mid-throughput sequencing has been a bottleneck, plagued by slow turnarounds and inflexible workflows.
The launch of the T1+ in 2025 broke this cycle by delivering 1.2 Tb of data with full PE150 workflow completion in just 24
hours—all while maintaining Q40 quality metrics exceeding 90%.
Designed for flexibility, the T1+
supports three flow cell formats and
leverages independent flow cell
lanes to handle multiple projects
simultaneously. Its optimized
internal design also minimizes
reagent consumption, maximizing
cost-efficiency. This combination of
speed, economy, and versatility
makes the T1+ the definitive
solution for accelerated discoveries
in tumor sequencing, WGS, whole
exome sequencing (WES), and
multi-omics studies. The T1+ launch.
18Leading Life Science Innovation
8� Conquering the extremes
In 2024, MGI proved that genomic innovation knows no
geographic bounds by successfully deploying the E25 and
G99 platforms at an altitude of 5,200 meters on Mount
Everest. Despite extremely low-temperature, low-oxygen
conditions, both sequencers delivered stable, high-quality
data. The portable E25 excelled in on-field sample testing,
showcasing its portability and low environmental
requirements. The G99 demonstrated benchtop
sequencing comparable to controlled lab environments
across six rounds of testing.
As well as the highest peaks, MGI’s research contributions
extend to the deepest oceans. Utilizing DNBSEQ
technology, researchers generated high-resolution
genome and metagenome data from samples in the
Mariana Trench.1,2,3 These insights advanced
understanding of adaptations to extreme environments
and provided evidence for ecological protection and
sustainable resource utilization.
9� Reaching global impact
Over the past decade, MGI has transitioned from an
emerging technology developer into a global
infrastructure, as evidenced by its pivotal role in 69
population-based studies worldwide. Key examples
include the South Africa 110K Human Genome Program,
which brought high-throughput sequencing to Africa at a
previously impossible scale, and the Brazil National
Genomics Program (Genomas Brasil), which is sequencing
100,000 genomes to advance rare disease research. MGI
also supports The Genomics Thailand Initiative to boost
the nation’s research competitiveness and medical
standards. By March 2025, this programme successfully
completed Phase One, including WGS of 50,000
individuals.
These efforts are closing the global data gap to improve regional disease prevention and treatment. MGI’s commitment
to global impact extends to the Million Microbiomes of Humans Project (MMHP), a 10-country collaboration to map the
microbial diversity of 1 million individuals.
The launch of the 110K Human Genome Program in South Africa.
The E25 on Mount Everest.
19Leading Life Science Innovation
Beyond population genomics, MGI has established leadership in specialized academic research, with its single-cell
platform contributing to over 120 SCI-indexed publications. Further cementing its research leadership, MGI launched the
DCS Lab Initiative in 2023, establishing 30 labs worldwide and providing end-to-end workflows for advanced research in
DNA genomics, cell omics, and spatial omics.
At the heart of MGI’s new era is the “SEQALL+GLI+Omics” vision. In February 2026, MGI Tech officially solidified this
strategy by announcing the acquisition of STOmics and CycloneSEQ. This move transformed MGI into a comprehensive
one-stop solution provider, offering a suite of short-read sequencing, long-read nanopore sequencing, generative lab
intelligence, and spatial omics technologies. Unifying these capabilities under one roof empowers MGI to meet the
increasingly diverse needs of global customers across multiple technology platforms.
10� Advancing beyond automation into lab intelligence
In 2025, MGI launched the Generative Lab Intelligence (GLI) department, a strategic upgrade of its legacy laboratory
automation business spearheading the life sciences industry’s paradigm shift from manual experience-led operations to
AI-driven, data-centric decision making. Built on a full-stack product portfolio spanning AI intelligent solutions, universal
automation hardware, computing and storage infrastructure, and end-to-end smart lab solutions, GLI enables seamless
scalability from benchtop research labs to industrial-scale production facilities, with a proprietary wet-dry closed-loop
system powered by multi-agent collaborative technology.
GLI Product Family From “centimeter-scale” laboratory to “factory-scale” production laboratory, it covers all scenarios�
Lab on Chip Lab on Desk Lab on Cube Lab as Factory
Automated Liquid Handling Platform Intelligent Digital Platform
Customized
Platform
Automated Devices
and Consumables
Integrated
Platform
Automatic Sampling Device Consumables
CDMO Integrated Solution
STP-3000
D4 SP-100 SP-960 SP-Smart 8 AlphaTool PrepALL
αLab Studio αCube
STP-7000 SP-NE32
MegaBOLT/ZBOLT
STP-B1000 SP-NEX SP-NE384
FLP-L50 FLP-L
Portable Smart Sampler-Water
AIO
Glab 50K
Sample Pretreatment
Sample Preparation
Nucleic acid extraction
Universal Pipetting
20Leading Life Science Innovation
By 2026, nearly a decade of evolution in liquid handling systems culminated in the launch of PrepALL, a highperformance, compact system that makes “smart pipetting” accessible to all. Parallel to this, MGI’s library preparation
has evolved into the All-in-One (AIO) Library Preparation and Sequencing System, which utilizes modular technology and
AI to create a seamless, closed-loop, “sample in, report out” workflow. This marks MGI’s evolution from applicationspecific instruments to a full-stack GLI portfolio spanning AI intelligent solutions, universal automation hardware,
computing and storage infrastructure, and end-to-end smart lab turnkey solutions, anchored by the breakthrough new
generation of liquid handling innovation with PrepALL.
The αCube Data Center Appliance, the core computing engine of the GLI ecosystem, integrates BT, IT, and AI to automate
complex bioinformatics via the αBP platform, accelerating WGS workflows and supporting large-scale genomic studies.
Complementing this is αLab Studio, the central intelligent brain of the framework, an AI-powered management platform
that enables full-process intelligent orchestration from experimental design to autonomous execution, bridging the gap
between automation and smart collaboration for end-to-end laboratory management. Validated by mega-scale national
genomic projects and global commercial deployments, this integrated GLI system empowers breakthroughs across
multi-omics research, biopharmaceutical R&D, clinical diagnostics, and public health—redefining industry standards for
autonomous, scalable and future-ready smart laboratories.
Conclusion
MGI’s journey over the last decade has been defined by an evolution from a sequencing hardware manufacturer into a
pioneer of integrated life sciences, now delivering a true‘ SEQALL+GLI+Omics’ one-stop solution. From supporting
national population cohorts to enabling research in the world’s most extreme environments, these milestones showcase
an ecosystem built for impact. As a global leader in integrated short-read, long-read, and spatial omics solutions, MGI
remains a vital partner in the effort to turn complex biological data into life-saving medicine.
Follow MGI’s journey here
References
1. Xiao X, Zhao W, Song Z, et al. Microbial ecosystems and ecological driving forces in the deepest ocean sediments. Cell. 2025;188(5):1363–1377. doi: 1016/j.
cell.2024.12.036
2. Zhang H, Sun S, Liu J, et al. The amphipod genome reveals population dynamics and adaptations to hadal environment. Cell. 2025;188(5):1378–1392. doi: 10.1016/j.
cell.2025.01.030
3. Xu H, Fang C, Xu W, et al. Evolution and genetic adaptation of fishes to the deep sea. Cell. 2025;188(5):1393–1408. doi: 10.1016/j.cell.2025.01.002
21Leading Life Science Innovation
Genomic Solutions Driving Innovation
The technology that powered MGI’s record-breaking achievements is at the heart of the portfolio presented here. This
section outlines how MGI’s proven technologies and solutions deliver the reliability and precision necessary to solve
your most complex sequencing challenges.
Key sequencing approaches
As the only company globally to master all three key sequencing signal detection modes—excited-luminous,
self-luminous, and non-luminous—MGI provides a level of versatility unmatched in the industry.
Excited-luminous
High-precision lasers hit DNA nanoballs (DNBs) on patterned array flow
cells, exciting fluorescent tags attached to DNA bases, which then emit light.
A P
C G
C A T
G T A T A C
Self-luminous
A portable solution where a biochemical reaction within the DNB generates
light when a base is incorporated, allowing an embedded complementary
metal-oxide-semiconductor (CMOS) sensor to capture the signal directly.
A P
A T
C A C
G T G T A C
A G
C T
C
Non-luminous
A solution for long-read sequences and real-time data. DNA passing
through nanopores generates unique electrical signatures for each
nucleotide, enabling accurate sequence identification.
22Leading Life Science Innovation
SEQ ALL sequencing platform
MGI distinguishes itself as the only global manufacturer capable of mass-producing both short-read and longread instruments, which have been unified into the SEQ ALL platform.
E25
• Self-luminous sequencing
• Ultra-portable
• Handles tasks from
sequencing to report
generation
• Daily data throughput
of up to 7.5 Gb
T20×2
• Excited-luminous
sequencing
• Ultra-high throughput
• Processes up to 6
slides per run
• Enables sub-$100 whole
human genome
sequencing
G99
• One of the fastest speeds
amongst medium- to
low-throughput
sequencers
• Optional built-in
bioinformatics module for
streamlined analysis
• Dual flow cell configuration
for flexible throughput
T1+
• Rapid benchtop sequencer
• Dual flow cell for
concurrent operation
• Three flow cell options for
flexibility
• One-click DNB preparation
and loading
DNA Nanoball Sequencing (DNBSEQ™) technology
Short-read sequencing at every scale, combining unmatched accuracy, speed, and efficiency.
23Leading Life Science Innovation
T7+
• Ultra-high throughput
• Annual capacity of 35,000
whole human genomes
• 7-in-1 intelligent workflow
• Over 90% of generated data
achieves a Q40 quality score
CycloneSEQ nanopore sequencing technology
Leverages non-luminous sequencing and an innovative base-calling algorithm model for accurate, real-time
base calling.
Sequencing consumables
Library prep kits and sequencing reagents for precise
library preparation and high-quality sequencing.
G100-ER
• Portable
• Rapid
• Two independent flow cells
for simultaneous operation
• Enables throughput of up
to 85 Gb
G400-ER
• Features a highthroughput, high-density
flow cell, combining long
read lengths, high data
output, and real-time
sequencing.
• Detects base modifications
• Suitable for complex
genomes
Learn more about SEQ ALL Sequencer products
24Leading Life Science Innovation
Generative Lab Intelligence (GLI)
AI-driven automation of liquid handling platforms streamlines sample pretreatment, nucleic acid extraction,
sample preparation, and pipetting.
Liquid handling system
All in one
PrepALL
• Excellent pipetting performance
• Cost effective
• Simplified setup and deployment
• Intelligent user experience
• Open-source hardware/software design
AIO
• Fully automated workflow from sample to answer
• Flexible sample throughput with independent pipetting
• Built-in self-luminous sequencer for fast turnaround time
PrepALL-pP8G
• Built upon PrepALL to fully integrate single-cell sorting and
proteomics workflows
• Ultra-high throughput parallel sorting
• Full-range precision dispensing
• AI-powered intelligent single-cell recognition
• Gentle thermal inkjet technology ensuring high cell viability
• Versatile applications across multiple proteomics methods
25Leading Life Science Innovation
SIRO-48
• Parallel sample processing allows fully unattended library preparation
• Integrated, closed-system workflows for data consistency
• Compact integration enables fast deployment across clinical or
research settings and reduces operating costs
Software and bioinformatics
αCube Data Center Appliance
• High-performance heterogeneous computing architecture provides
extreme computing power
• Large capacity and high-density storage
• AI-powered bioinformatics analysis
• Elastic scalability and easy expansion for flexibility
αLab studio
• Intelligent scheduling system (Nexus) leverages AI to orchestrate tasks,
equipment, and personnel for stable, high-throughput workflows
• Laboratory information management system (LIMS) provides
end-to-end digital lifecycle management, enabling standardization,
traceability, and quality control
• Sample management system (SMS) delivers full-chain sample tracking
from intake to transfer, ensuring data integrity, consistency, and
regulatory compliance
• Electronic laboratory notebook (ELN) captures and archives data for
excellent reproducibility and auditability
• Digital twin (DT) system builds a real-time virtual lab for simulation,
monitoring, predictive analysis, and system-level optimization
© 2025 MGI All rights reserved.
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Learn more about GLI products
26Leading Life Science Innovation
Multi-Omics
In 2025, MGI elevated its Novel Business segment into a dedicated Multi-Omics business unit—a strategic move at
the heart of its “Full-Life Digitization” vision. This unified ecosystem brings together DNA genomics, cell omics,
spatial omics, proteomics, mass spectrometry, automated biobanking, and ultrasound imaging, empowering
researchers with a holistic toolkit that captures biological complexity across dimensions.
PopOmics
Integrated high-throughput sequencing solutions with end-to-end
automation for population-scale genomic, methylation,
transcriptomic, and metagenomic studies.
Cell Omics
Supports sample encapsulation and library prep for single-cell research. Combined with MGI’s other
technologies, it covers end-to-end workflows from storage and transport to data analysis.
TaiM 4
• Part of MGI’s one-stop DNBelab C Series platform
• Compact, portable droplet generator for 1–4 single-cell
samples per run
• Supports scRNA-seq and scATAC-seq with fast, high-throughput
encapsulation using dual-bead microfluidics
YellowR 16
• Stable power through precise negative pressure-driven oil-in-water
droplet generation
• Supports flexible loading of 1–4 samples
• Supports diverse library preparation methods
27Leading Life Science Innovation
DNBelab C series high-throughput single cell RNA
library preparation set v3.0
• Sensitive detection of genes
• 1–4 samples per run to choose from flexibly
• Efficient and stable cells recovered
• Fast droplet generation
• Accurately identifies multiple cell beads
STOmics
An array of products for mapping gene and protein expression at single-cell resolution.
Stereo-seq Transcriptomics Solution v1.3
• High Sensitivity: Superior capture efficiency delivering significantly
higher gene counts per cell
• Flexibility: Supports multiple chip sizes (up to 13 cm x 13 cm) and
broad species/tissue compatibility
• Unbiased Discovery: Limitless whole-transcriptome profiling even for
low-quality (low RIN) samples
Stereo-seq OMNI Transcriptomics for FFPE Solution v1.1
• Enhanced FFPE Performance: 1× to 3× higher sensitivity for deeper
biological insights from clinical samples
• True Single-Cell Resolution: Superior diffusion control ensures
precise cell-level annotation and stratification
• Optimized Data Yield: Over 100% increase in usable data for more
efficient clinical research
Stereo-CITE Proteo-Transcriptomics Solution v1.1
• Multi-omics Integration: Simultaneously captures spatial RNA
and 100+ protein markers in a single tissue section
• Advanced Synergy: Combines the power of Stereo-seq and
CITE-seq technologies
28Leading Life Science Innovation
Go Spatial
• Highly Automated: Achieves automation of post-imaging biochemical
reactions built around Stereo-seq slide cassettes, reducing manual
intervention steps and batch-to-batch variability
• Consistent and Reliable Performance: Precision pipetting and
temperature control deliver highly reproducible, standardized results
• User-Friendly: An intuitive graphical interface that simplifies user
training and streamlines experimental workflow
G400RS FluoXpert
• Enables seamless switching between automated high-throughput
sequencing and fluorescence staining and imaging
• AI-powered multiplex immunofluorescence (mIF) image analysis
solution
PMIF-20
• Fully automated staining and imaging system
• Leverages mIF technology to capture precise spatial protein expression
data in tissue sections
Proteomics
Learn more about multi-omics products
29Leading Life Science Innovation
Gas chromatography–mass spectrometry
In addition to the DNA, cell, spatial, and proteomics (DCSP) suite, the integration of mass spectrometry
introduces small molecule detection—such as metabolomics and lipidomics—to the multi-omics ecosystem for
the first time.
7700B GC-MS
• Utilizes an inert ceramic electron ionization (EI) source
• Equipped with a pre-quadrupole
• Instrument detection limit (IDL) of <10 fg for ultra-trace analytes
• Exceptional signal-to-noise (S/N) ratio
• Features a discontinuous discrete electron multiplier
• Streamlines workflows with auto-shutdown, flow protection, and batch
data processing
• Qualification Safety Standard (CE): Compliant with EN 61010-
1:2010+A1:2019
• Testing and Certification: DEKRA Test Report No. 2250100R.51A,
Result: Pass
• ISO Certifications:
• ISO 9001 (QMS): Certificate No. 123725Q10183R0M
• ISO 14001 (EMS): Certificate No. 123725E10151R0M
• ISO 45001 (OH&S): Certificate No. 123725510152R0M
• Validity: Production license valid until June 3, 2029; ISO certificates
valid until September 3, 2028
30Leading Life Science Innovation
Sample storage
Automated biobanking solutions engineered for the safe, long-term storage of valuable biological samples.
Featuring fully automated sample access, high storage capacity, and intelligent management, delivering precise,
efficient, and reliable services for modern biobanks and research centers.
Automated low-temperature biobanking
CLab-RG Series
• Low-temperature automated sample storage system
• Temperature range: 4 °C/-20 °C
• Fully automated and efficient access capabilities
• Customizable solutions to address large-scale sample storage
requirements
CLab-LT Series
• Ultra-low temperature automated sample storage system
• Enables large-scale sample preservation at -80 °C
• Fully automated and efficient access capabilities
• Customizable solutions to address large-scale sample storage
requirements
CLab-FZ Series
• Enables large-scale sample preservation at -80 °C
• Triple cooling system: -80 °C, -20 °C, with LN2 backup
• Supports automated access to single tubes and whole boxes
• 90K/150K tubes storage capacity options
• Automatic defrosting with air cooling
• Emergency sample retrieval through maintenance door
31Leading Life Science Innovation
Automated cryogenic sample storage
Auxiliary product
CLab-LN55K Pro
• Provides a vapor phase liquid nitrogen storage environment: The top of
the tank is < −180 °C, and the tube-picking area is ≤ −150 °C
• Supports automated access to single tubes and whole boxes
• Compatible with SBS standard format cryogenic tubes
• Storage capacity: 0.5 mL ≥ 55K tubes; 2 mL ≥ 24K tubes
CLab Capper
• A benchtop instrument custom-designed for SBS-format cryotubes
• Adapts to end-to-end automated workflows
• A single capping/uncapping operation takes ≤ 20 seconds
32Leading Life Science Innovation
Ultrasound platform
Built around a smart healthcare ecosystem of intelligence, remote connectivity, and automation, MGI delivers
accessible, intelligent ultrasound services to remote areas, emergency scenes, and community settings worldwide.
R3
• The world’s first remote ultrasound robot requiring no onsite specialist,
enabling real-time expert diagnosis via 5G
• From ICU and emergency to ambulances and remote field sites
• Supports in-hospital, pre-hospital, community, and off-site scenarios
• Quick deployment for frontline, rural, and international rescue missions
• Enables seamless collaboration across departments and locations
EF6-CL
• C-Convex (2–5 MHz) and L-Linear (4–13 MHz); one-touch switching
• For superficial tissues (thyroid, vessels, muscles) and deep tissues
(abdomen, obstetrics)
• One-click expert consultation with real-time, AI-assisted diagnosis
• Voice control, wireless fast charging, IPX7 waterproof, lightweight, and
multiple modes
33Leading Life Science Innovation
Applications
Onco-genomics
The DNBSEQ platform has served as the global platform of choice for
oncology, supporting third-party adaptations for cancer diagnostics in
Portugal, breast cancer diagnostics in Japan, and proactive genetic
screening for breast cancer in Italy.
Environment and biodiversity
MGI has enabled landmark ecological studies that are changing the face of
biodiversity research, advancing our understanding of how environments
shape microbial communities in extreme environments and driving
mangrove conservation efforts in Thailand.
Public health
MGI provides rapid-response solutions for the genomic surveillance of
emerging viruses, such as Nipah, chikungunya, and monkeypox, while
supporting long-term research into “elite controllers” of HIV in South Africa.
Agriculture and food safety
In Australian horticulture, a major genomics initiative utilizes MGI’s highthroughput sequencing and automation platforms to optimize crop yield,
quality, and climate resistance.
Archaeology
The ancient genome of the Chinese Emperor Wu of Northern Zhou was
sequenced using the G99, providing insights into his appearance, disease
susceptibility, and ancestry.
Molecular breeding
Molecular breeding is becoming more accessible through MGI’s low-pass
whole-genome sequencing, which is being utilized in Latin America to
enhance the breeding and genetic improvement of crops.
MGI’s sequencing technologies are more than just advanced hardware; they are
the engines driving global breakthroughs. Explore the details of research successes
in the case studies below.
34Leading Life Science Innovation
Global Impact: MGI in Action
Whether navigating Thailand’s wild mangroves, Portugal’s extensive vineyards, or the controlled precision of Colombia’s
clinical labs, MGI’s sequencing technology is empowering researchers and healthcare providers worldwide to address
critical challenges in environmental conservation, agricultural sustainability, and precision medicine. These three stories
showcase how accessible, high-quality genomic tools are driving discovery and innovation across continents.
Protecting Thailand’s Coastal Ecosystems
For centuries, mangroves have served as Thailand’s coastal
guardians—natural barriers protecting communities from
coastal erosion and storm surges while providing critical
habitat for marine species. Yet over the past 50 years, more
than 60% of Thailand’s mangrove forests have disappeared,
leaving coastal communities increasingly vulnerable.
Dr. Jeremy Shearman, Senior Researcher at Thailand’s
National Omics Centre (NOC), explained the urgency:
“Mangroves are essential for coastal regions and
estuaries. They offer erosion protection from surf and
storm damage, and they provide nurseries for young
marine life that replenish ocean stocks.”
Dr. Jeremy Shearman
Senior Researcher
Thailand’s National Omics Centre
Dr. Wirulda Pootakham
Director
Thailand’s National Omics Centre
35Leading Life Science Innovation
Achieving effective conservation of these regions requires a deep understanding of the ecosystem at a genetic level. To
assess mangrove genetic diversity, the team set out to build comprehensive reference genomes and shed light on
genetic variation across different mangrove populations—all while maintaining cost-effectiveness for large-scale
environmental monitoring.
NOC partnered with MGI to deploy the G400RS sequencer, utilizing two complementary approaches: restriction-site
associated DNA sequencing (RAD-seq) for population structure analysis, and RNA sequencing to reveal adaptive
mechanisms in high-salt environments.
Genomic analysis revealed distinct genetic subpopulations of mangroves, separated by natural mountain barriers, with
flower size emerging as a key factor influencing population subdivision. Alarmingly, the data indicate that popular
mangrove species are losing their genetic diversity because replanting relies on seeds from a limited, uniform gene pool.
“Building a reference genome database for 15 mangrove species allows us to assess genetic diversity more accurately,”
explained Dr. Wirulda Pootakham, Director of NOC. “This is vital for prioritizing conservation efforts.”
The genetic maps that were generated now enable science-based restoration strategies that preserve local genetic
resilience, directly supporting Thailand’s HM King Rama IX International Botanical Garden for Mangroves—the world’s
first botanical garden collecting all global mangrove species.
Watch the full story
36Leading Life Science Innovation
Turning Dust Into Data: Agricultural Innovation in Portugal
In southern Portugal, an unexpected environmental
phenomenon is transforming agricultural research. Saharan
dust events are now twelve times more frequent due to
climate change, transporting millions of microorganisms
across the Mediterranean, profoundly altering soil and
plant microbiomes in Portuguese vineyards.
With support from MGI’s G99 platform, researchers at the
University of Lisbon have been mapping the microbial
composition of dust, soils, and plants to understand how
these bioaerosols affect grape quality, disease resistance,
and crop yields. The high-sensitivity sequencing enables
real-time analysis of millions of microorganisms, allowing
early risk detection and identification of biotechnological
opportunities.
“The impact of dust is bidirectional,” explained Prof.
Ricardo Dias, researcher at the University of Lisbon. “It
can bring risks that threaten productivity, but it also
carries microorganisms with biotechnological potential.
We need to monitor and understand both sides.”
During Storm Célia, which in 2022 deposited Saharan dust
across regions of Spain, the team identified a bacterial
genus with the potential to act as a natural fertilizer.
They’ve also been testing non-native microbial consortia
that increase vineyard resilience, improve grape quality,
and reduce pesticide dependency.
“Our partnership with the University of Lisbon
demonstrates how sequencing can turn dust into data—
starting in vineyards but ultimately building a system of
microbial intelligence for agriculture at large,” stated
Duncan Yu, President of MGI.
Professor Ricardo Dias
Researcher
University of Lisbon
Watch the full story
37Leading Life Science Innovation
In Brazil, access to advanced genomic diagnostics has
historically been limited by high costs and infrastructure
challenges. Yet the nation’s healthcare landscape is
undergoing a dramatic transformation through a strategic
alliance between MGI and Dasa, the largest medical
diagnostics company in Latin America.
In 2024, Dasa partnered with MGI to implement a
comprehensive genomic sequencing workflow across its
laboratory network. The installation includes MGI’s
high-throughput T7 sequencer, automated sample
preparation systems SP-100 and SP-960, and the ZTRON
data platform. This approach creates an integrated
solution that significantly increases laboratory efficiency
while reducing processing time and overall costs.
“Our expertise in specialized health services combined
with MGI’s sequencing technologies will ensure greater
access for Brazilian patients to precision genomics,”
explained Gustavo Riedel, Director of Genomics LATAM at
Dasa. “This will help in defining more accurate and effective
treatments for illnesses such as cancers and rare diseases.”
Transforming Healthcare Access in Brazil:
MGI and Dasa Advance Precision Medicine
Gustavo Riedel
Director of Genomics LATAM
Dasa
38Leading Life Science Innovation
Learn more about collaborating with MGI
The impact extends beyond technical capabilities. By making genomic testing more accessible and affordable, the
partnership is democratizing precision medicine in Brazil. Patients who previously would have faced prohibitive costs or
long wait times can now access the genetic insights needed for personalized treatment decisions.
“With the new platform, we have gained a lot in quality, timeliness, productivity, standardization of routine processes
and data processing,” Riedel noted. “We want to guarantee more access for the population, in the shortest possible
time, at an increasingly affordable cost.”
Carlos Carpio, MGI’s General Manager for Latin America, emphasized the broader vision: “We are excited to leverage
MGI’s technology and Dasa’s expertise in the diagnostics sector and extensive healthcare network. We will help enhance
Dasa’s ability to serve an increasing number of patients by processing high-quality genetic samples that are more
accessible and efficient.”
The partnership represents more than technology implementation; it highlights a commitment to strengthening
genomics infrastructure throughout Latin America’s largest nation, advancing personalized medicine, and ensuring that
cutting-edge healthcare reaches the populations that need it most.
Watch the full story
39Leading Life Science Innovation
A Lifelong Journey of Genomic
Discovery: Reflecting on a Decade of
DNBSEQ Innovation and Beyond
Commentary by Dr� Radoje Drmanac,
CSO of MGI / Co-Founder of Complete Genomics
August 2025
This year marks a decade since DNBSEQ technology, painstakingly created and developed by my team and me, was
commercialized. As a father and a grandfather myself, DNBSEQ is my other baby—or not so much a baby now. At 10 years
old, I imagine it as on the cusp of adolescence, running around with friends and thinking and sounding almost like a
“grown-up”.
The last 10 years went by in a blink, and as I reflect on my journey in genomics (which spans far beyond these 10 years), I
am filled with pride and awe at how far we as an industry have come.
Making my mark
When I started college in Serbia studying molecular
biology in 1977, the Sanger and Maxam–Gilbert
sequencing methods were invented. Then, in 1986, the
world welcomed the first commercial DNA sequencer, the
ABI Prism 370A, touting a throughput of 1,000 bp per day.
A year later, I invented sequencing by hybridization and
soon after DNA microarrays as the first massively parallel
sequencing (MPS) solution for efficient genome
sequencing. In 1991 I moved with my team from Serbia to
Argonne National Laboratories as part of the Human
Genome Project (HGP), which became a pivotal moment
that set the stage for the revolutionary advancements we
see today. The project was not just about mapping the human genome; it was about unlocking the secrets of life itself. I
proposed and developed DNA sequencing-by-hybridization, which laid the groundwork for more efficient and higherthroughput sequencing methods.
Arriving at a turning point
The HGP marked the beginning of a new era in biology, akin to sending humans to the moon. It showed us that largescale projects were feasible and sparked a demand for sequencing more genomes. The project made shorter reads more
usable by providing a reference genome, enabling exome and panel sequencing. It was personally also a “light bulb
moment”, inspiring me to start Complete Genomics, with the goal of maximizing the potential of MPS.
40Leading Life Science Innovation
In 2005, amidst the arrival of next-generation sequencing, my team and I invented patterned arrays of DNA nanoballs (DNB),
which significantly expanded MPS’ capabilities and became the DNBSEQ sequencing platform. This technology offers
unparalleled accuracy, eliminating clonal errors and index hopping while generating higher signal density. It was the key to
Complete Genomics achieving the milestone of sequencing a human genome for $5,000 in 2010, demonstrating that routine,
affordable, and accurate whole-genome sequencing was not only possible but also beneficial. Our merger with MGI allowed
us to further develop DNBSEQ and introduce the BGISEQ-500, the first commercial sequencer based on DNBSEQ, in 2015.
Witnessing the fruits of our endeavors
I recall the watershed moment when we decided to expand beyond just providing whole human genome sequencing
services and develop our own commercial sequencer. At the time, we did not have a dedicated engineering or
technology development arm. I advised starting an engineering team in MGI, and this led to the hiring of senior engineer
Yongwei Zhang, who spoke both English and Chinese to help bridge the gap between the two sites. Yongwei, who has
remained at MGI, was instrumental in building the BGISEQ-500. I vividly recall the wave of emotions that swept over me
as I saw the machine for the first time, and I was even more astonished to see not just one—but 50 and even 100 of them
—in production.
Over the past decade, we have continually pushed the envelope in what DNBSEQ can do to global critical acclaim. To
date, users from 100 countries and regions across six continents have published more than 10,000 high-level articles
using the DNBSEQ platform, involving more than 5,406 species studied and fully verifying its advantages in data quality
and many other aspects. DNBSEQ now serves as the backbone of MGI’s suite of cutting-edge sequencing instruments,
including the versatile G400 benchtop sequencer, and the ultra-fast T7 with a throughput of 1–7 Tb per day. More
recently, we also launched the T1+, one of the fastest T-level benchtop sequencers globally with the capability of
completing a sequencing workflow in only 24 hours.
Indeed, genomics has advanced at an incredible pace, with sequencing costs falling dramatically. From the $3 billion
spent on the first human genome to sub-$100 genomes made available today by way of our T20×2 ultra-high
throughput sequencer, this journey has surpassed Moore’s Law predictions. I have long envisioned a future where
molecular health monitoring becomes an integral part of everyday life. These recent developments in DNBSEQ are
making routine genome sequencing for all a more tangible reality than ever. My team and I are determined to reach a $10
genome through advancements like increased DNB array density, our single-tube long fragment read (stLFR) technology,
CycloneSEQ technology, and other novel technologies, enabling affordable fully phased, highly accurate, and complete
whole-genome sequencing for health monitoring, personalized medicine, and other applications.
Welcoming a future of unlimited possibilities
The journey from when nucleic acids were first isolated in 1869, to the HGP, and the current era of genomics has been a
testament to human ingenuity and collaboration. The applications of sequencing technologies are vast and ever
expanding. I look forward to celebrating 10 years of the G400 or 10 years of the T7, and I’m excited about what these
platforms will bring to genomics and life science in the coming years.
In this past decade since DNBSEQ was commercialized, it has not only transformed the field of genomics but also
empowered numerous national genome projects around the world and paved the way for improved global health. As
DNBSEQ continues to evolve, we prepare to leverage its potential and ring in a new era where genomics will touch every
aspect of our lives, promising a future where health and longevity are within our grasp. This year, we are not just
celebrating a milestone; we are embracing the limitless possibilities of DNBSEQ that lie ahead.
41Discover the power of the T7+
The End of
Compromise
T7+
Ultra-high throughput
meets unparalleled
efficiency
The T7+ delivers over 14 terabases of
high-quality data within 24 hours,
providing an annual capacity of up to
35,000 whole-genome sequences.
7-in-1 intelligent
integration
From DNB preparation to
sequencing, the T7+ provides a fully
automated, streamlined workflow
that reduces manual intervention
and accelerates time-to-results.
Designed for
accuracy at scale
Whether you’re conducting
population genomics, cancer
research, or multi-omics studies, the
T7+ handles your most demanding
projects with clinical-grade accuracy.Leading Life Science Innovation
Resources
Explore MGI’s cutting-edge technologies and real-world applications through a
wide range of videos. From product demonstrations to expert interviews,
discover how MGI is advancing genomics and empowering scientific discovery
across precision medicine, research, and beyond.
Video Library
Dive into the fascinating world of genomic science with an expert-led webinar
series. Learn from top scientists as they explore the latest applications and
innovations transforming genomics research and clinical practice.
Webinar
Join MGI for engaging conversations about the genomics revolution. Whether
you’re a seasoned researcher or new to the field, this podcast features in-depth
discussions and interviews with leading experts who are shaping the future of
genomic science.
Podcast
As a global genomics company, MGI is committed to developing innovative
technologies that improve lives around the world. The latest ESG Report
outlines MGI’s latest progress, challenges, and priorities as they work toward a
more sustainable future.
ESG Report
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