Explore All Products
  • Sequencing Platforms
  • Microarray Scanners
  • IVD Instruments

All Instruments

Illumina financial solutions
Illumina financial solutions

Access the latest technology today with flexible financing for instruments and reagents

Learn more
  • Library Preparation Kits
  • Sequencing Reagents
  • Microarray Kits
  • Clinical Research Products
  • IVD Products

All Kits & Reagents

NextSeq 1000 and NextSeq 2000 Reagents
NextSeq 1000 and NextSeq 2000 Reagents

XLEAP-SBS chemistry on NextSeq 1000 and NextSeq 2000 enables faster and higher quality sequencing than ever before

Learn more
  • Library Prep & Array Kit Selector
  • Gene Panel & Array Finder
  • DesignStudio Custom Assay Designer
  • TruSight Oncology 500 Product Selector

All Selection & Planning Tools

Sequencing Platform Comparison Tool
Sequencing platform comparison

Compare NGS systems and find the one that's right for your needs

Find the right system
  • BaseSpace Sequence Hub
  • DRAGEN Secondary Analysis
  • Illumina Connected Analytics
  • Emedgene
  • Illumina Connected Insights
  • Clarity LIMS
  • Correlation Engine
  • Microarray Software

All Software & Informatics Products

DRAGEN v4.3 now available on-premises and on-cloud
DRAGEN v4.3 now available on-premises and on-cloud

Next-generation multigenome mapper, expanded ORA compression capability, and more

Learn more
  • Sequencing Services
  • Microarray Services
  • Proactive Instrument Monitoring
  • Instrument Services & Training

All Services

Illumina Proactive Instrument Performance Service
Illumina Proactive Instrument Performance Service

Our instrument performance service helps reduce unplanned downtime and minimize instrument requalification

Learn More
  • AmpliSeq for Illumina
  • Illumina Complete Long Reads
  • COVIDSeq Assay (96 samples)
  • Illumina DNA Prep
  • Illumina RNA Prep with Enrichment
  • NextSeq 1000 & 2000 Sequencing Systems
  • TruSight Oncology Product Family

All Popular Products

Do more, faster than ever
Do more, faster than ever

Deeper studies, more samples, more modalities. The NovaSeq X and 25B flow cell make ultra-high depth multiomics more accessible.

Learn more
See All Learning Options
Research Applications
  • Cancer Research
  • Microbiology
  • Agrigenomics
  • Complex Disease Genomics
  • Cellular & Molecular Biology
Clinical Applications
  • Reproductive Health
  • Oncology
  • Genetic & Rare Diseases

All Areas

Next-generation sequencing for beginners
Next-generation sequencing for beginners

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

Learn about NGS
Sequencing
  • DNA Sequencing
  • RNA Sequencing
  • High-Throughput Sequencing
  • Library Preparation
Microarrays
Multiomics
  • Genomics
  • Transcriptomics
  • Proteomics
  • Epigenomics
Other Popular Applications

All Techniques

Next-generation sequencing for beginners
Next-generation sequencing for beginners

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

Learn about NGS
NGS for Beginners
Our Technologies
  • Next-Generation Sequencing
  • Long-Read Sequencing
  • Microarray Technology
Sequencing Method Explorer

All Technologies

Next-generation sequencing for beginners
Next-generation sequencing for beginners

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

Learn about NGS
Genomics Research Hub
  • Genomics Articles
  • Illumina Publications
  • Open-Source Bioinformatics Tools
Next-generation sequencing for beginners
Next-generation sequencing for beginners

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

Learn about NGS
Illumina Resources & Tools
NGS for Beginners
Genomics Education
  • Illumina NGS & Array Training
  • Educational Webinars
  • Support Webinars & Online Training
  • Videos
  • Podcasts
Medical Genetics

All Training

Next-generation sequencing for beginners
Next-generation sequencing for beginners

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

Learn about NGS
Peer-Reviewed Publications
  • Illumina Publications
  • Publication Summaries
Customer Stories
  • iCommunity Interviews
  • Customer Videos
  • More Stories
Next-generation sequencing for beginners
Next-generation sequencing for beginners

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

Learn about NGS
Infrastructure & Pipeline Setup
Sequencing Data Analysis
Biological Data Interpretation

All Informatics Education

Next-generation sequencing for beginners
Next-generation sequencing for beginners

Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started.

Learn about NGS
See All Company Info
  • Office Locations
  • Management Team
  • Board of Directors
  • Ethics Advisory Board
  • Fact Sheet
  • iHope Philanthropic Sequencing
  • Governance & Code of Conduct

More About Us

This is the Genome Era
This is the Genome Era

Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

Watch now
News Center
  • Feature Articles
  • Perspectives Blog
  • Press Releases
  • Illumina in the News
  • Illumina Images
Events & Webinars
  • Illumina Genomics Forum
This is the Genome Era
This is the Genome Era

Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

Watch now
  • Overview
  • Search Jobs
  • Career Tracks
  • Employee Stories
  • Illumina Locations & Benefits

More Career Info

This is the Genome Era
This is the Genome Era

Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

Watch now
  • Overview
  • Accelerate Access to Genomics
  • Empower Our Communities
  • Integrate Sustainability
  • Nurture Our People
  • Advance Diversity, Equity, & Inclusion
  • Operate Responsibly
  • ESG Hub
This is the Genome Era
This is the Genome Era

Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

Watch now
  • Overview
  • Shareholder Events
  • Financial Information
  • Stock Information
  • Corporate Governance

All Investor Information

This is the Genome Era
This is the Genome Era

Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

Watch now
  • MyIllumina Customer Dashboard
  • Financial Solutions
  • Instrument Buying Options
  • Distributors
  • Suppliers
  • Illumina for Startups
  • Partnerships
  • Contact Us

More Business Solutions

This is the Genome Era
This is the Genome Era

Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

Watch now
  • Terms & Conditions
  • Report a Compliance Issue
  • Privacy
  • Governance & Code of Conduct

All Legal Information

This is the Genome Era
This is the Genome Era

Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world

Watch now
View All Support
  • Instrument Support
  • Library Prep Kit Support
  • Microarray Support
  • Software Support
Illumina DRAGEN Secondary Analysis v4.0
Illumina DRAGEN Secondary Analysis v4.3

Get instructions for using DRAGEN Secondary Analysis v4.3

Learn more
  • Documentation
  • Technical Bulletins
  • Illumina Adapter Sequences
  • Support Webinars & Online Training
  • Instructor-Led & Other Training
Illumina DRAGEN Secondary Analysis v4.0
Illumina DRAGEN Secondary Analysis v4.3

Get instructions for using DRAGEN Secondary Analysis v4.3

Learn more
  • Sequencing Coverage Calculator
  • Custom Protocol Selector
  • Library Prep & Array Kit Selector
  • Gene Panel and Array Finder

All Support Tools

Illumina DRAGEN Secondary Analysis v4.0
Illumina DRAGEN Secondary Analysis v4.3

Get instructions for using DRAGEN Secondary Analysis v4.3

Learn more
  • Proactive Instrument Monitoring
  • Qualification Services

All Product Support Services

Illumina DRAGEN Secondary Analysis v4.0
Illumina DRAGEN Secondary Analysis v4.3

Get instructions for using DRAGEN Secondary Analysis v4.3

Learn more
  • Certificates (CofC, CofA) and Master Lot Sheets
  • Safety Data Sheets
  • Share Desktop
Illumina DRAGEN Secondary Analysis v4.0
Illumina DRAGEN Secondary Analysis v4.3

Get instructions for using DRAGEN Secondary Analysis v4.3

Learn more
  • Distributors
  • Suppliers
  • Medical Information & Resources
  • All Contact Info
Illumina DRAGEN Secondary Analysis v4.0
Illumina DRAGEN Secondary Analysis v4.3

Get instructions for using DRAGEN Secondary Analysis v4.3

Learn more
Change Selected Area of Interest
Cancer Genomics Research
  • Cancer Sequencing Methods
  • Immuno-Oncology Research
  • Cancer Epigenetics
  • All Cancer Genomics Research
Clinical Cancer Research
  • Somatic Mutations
  • Germline Mutations
  • Tumor Mutational Burden
  • All Clinical Cancer Research
Illumina Training
TruSight Oncology 500 ctDNA v2 is now available
TruSight Oncology 500 ctDNA v2 is now available

Improved sensitivity using lower cfDNA input, a faster turnaround time, and a more streamlined workflow

Learn more
  • TruSight Oncology 500 Product Family
  • AmpliSeq for Illumina Cancer Hotspot Panel v2
  • AmpliSeq for Illumina Comprehensive Cancer Panel
  • iSeq 100 System
  • NextSeq 2000 System

All Cancer Research Products

TruSight Oncology 500 ctDNA v2 is now available
TruSight Oncology 500 ctDNA v2 is now available

Improved sensitivity using lower cfDNA input, a faster turnaround time, and a more streamlined workflow

Learn more
  • Library Prep & Array Kit Selector
  • Gene Panel & Array Finder
  • Sequencing Coverage Calculator
  • Custom Protocol Selector

More Tools

TruSight Oncology 500 ctDNA v2 is now available
TruSight Oncology 500 ctDNA v2 is now available

Improved sensitivity using lower cfDNA input, a faster turnaround time, and a more streamlined workflow

Learn more
  • BaseSpace Sequence Hub Apps
  • BaseSpace Variant Interpreter
  • BaseSpace Correlation Engine
  • DesignStudio Custom Assay Designer
All Informatics Products
TruSight Oncology 500 ctDNA v2 is now available
TruSight Oncology 500 ctDNA v2 is now available

Improved sensitivity using lower cfDNA input, a faster turnaround time, and a more streamlined workflow

Learn more
Customer Interviews
  • Breast Cancer Target Identification with High-Throughput NGS
  • Polygenicity of Cancer
  • NGS Panels in Brain Tumor Studies
Featured News
  • Driving Single Cell Research
  • The Promise of Liquid Biopsies
  • The Complex World of Pan-Cancer Biomarkers
TruSight Oncology 500 ctDNA v2 is now available
TruSight Oncology 500 ctDNA v2 is now available

Improved sensitivity using lower cfDNA input, a faster turnaround time, and a more streamlined workflow

Learn more
Microbial Sequencing Methods
  • 16s & ITS rRNA Sequencing
  • Metagenomic Sequencing
  • Microbial Whole-Genome Sequencing
  • Microbial Transcriptomics
Infectious Diseases
Human Microbiome Analysis
Illumina Training

All Microbial Genomics Research

“Tripledemic” pathogen surveillance is critical
“Tripledemic” pathogen surveillance is critical

On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants

Read article
  • Illumina COVIDSeq Test
  • Illumina DNA Prep
  • Illumina RNA Prep with Enrichment
  • iSeq 100 System

All Microbial Genomics Products

“Tripledemic” pathogen surveillance is critical
“Tripledemic” pathogen surveillance is critical

On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants

Read article
  • Library Prep & Array Kit Selector
  • Sequencing Coverage Calculator
  • Custom Protocol Selector

More Tools

“Tripledemic” pathogen surveillance is critical
“Tripledemic” pathogen surveillance is critical

On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants

Read article
  • BaseSpace Sequence Hub Apps
  • BaseSpace Correlation Engine
  • Coronavirus Software Tools
  • SRST2 BaseSpace App

All Informatics Products

“Tripledemic” pathogen surveillance is critical
“Tripledemic” pathogen surveillance is critical

On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants

Read article
Customer Interviews
  • Microbiome Studies Help Refine Drug Discovery
  • Investigating the Mysterious World of Microbes
Featured News
  • Coronavirus Characterization
  • IDbyDNA Partnership on NGS Infectious Disease Solutions
  • Mapping Stockholm's Subway Microbiome

More News

“Tripledemic” pathogen surveillance is critical
“Tripledemic” pathogen surveillance is critical

On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants

Read article
  • Agrigenomics
  • Plant & Animal Genotyping
  • Plant & Animal Sequencing
  • Commercial Agricultural Applications
  • Agrigenomics Consortia
  • Illumina Training
The race results are in—with marine genomic data
The race results are in—with marine genomic data

Sport sailors can use these environmental DNA collection kits even at full speed

Read article
  • Illumina DNA Prep
  • Infinium iSelect Custom Genotyping BeadChips
  • NovaSeq 6000 System

All Agrigenomics Products

The race results are in—with marine genomic data
The race results are in—with marine genomic data

Sport sailors can use these environmental DNA collection kits even at full speed

Read article
  • Library Prep & Array Kit Selector
  • Gene Panel & Array Finder
  • DesignStudio Custom Assay Designer

More Tools

The race results are in—with marine genomic data
The race results are in—with marine genomic data

Sport sailors can use these environmental DNA collection kits even at full speed

Read article
  • BaseSpace Sequence Hub Apps
  • GenomeStudio Software

All Informatics Products

The race results are in—with marine genomic data
The race results are in—with marine genomic data

Sport sailors can use these environmental DNA collection kits even at full speed

Read article
Customer Interviews
  • How Genomics Changed Herd Management
  • Large-Scale Bull Genome Sequencing
Featured News
  • 2020 Agricultural Greater Good Grant Winner
  • 2019 Agricultural Greater Good Grant Winner
  • Earth BioGenome Project

More News

The race results are in—with marine genomic data
The race results are in—with marine genomic data

Sport sailors can use these environmental DNA collection kits even at full speed

Read article
Complex Disease Genomics
  • Disease Association Studies
  • Gene Target Identification & Pathway Analysis
  • Polygenic Risk Scores
  • Methods
Illumina Training
Shriners Children’s and specialized pediatric care
Shriners Children’s and specialized pediatric care

The institution is taking its research global, collecting international samples to find disease-associated variants

Learn more
  • Infinium MethylationEPIC Kit
  • TruSeq Methyl Capture EPIC Library Prep Kit
  • Infinium Global Screening Array
  • Infinium PsychArray BeadChip
  • NextSeq 2000 System

All Complex Disease Research Products

Shriners Children’s and specialized pediatric care
Shriners Children’s and specialized pediatric care

The institution is taking its research global, collecting international samples to find disease-associated variants

Learn more
  • Library Prep & Array Kit Selector
  • Gene Panel & Array Finder
  • Sequencing Coverage Calculator
  • Custom Protocol Selector

More Tools

Shriners Children’s and specialized pediatric care
Shriners Children’s and specialized pediatric care

The institution is taking its research global, collecting international samples to find disease-associated variants

Learn more
  • BaseSpace Sequence Hub Apps
  • BaseSpace Variant Interpreter
  • BaseSpace Correlation Engine
  • Microarray Software

All Informatics Products

Shriners Children’s and specialized pediatric care
Shriners Children’s and specialized pediatric care

The institution is taking its research global, collecting international samples to find disease-associated variants

Learn more
Customer Interviews
  • Polygenic Risk Scores
  • Genetic Contributions of Cognitive Control
  • Rare Disease Variants in Infants
Featured News
  • Every Diagnosis Matters
  • The Story of Tree Baby
  • Mysteries of Rare & Undiagnosed Diseases

More News

Shriners Children’s and specialized pediatric care
Shriners Children’s and specialized pediatric care

The institution is taking its research global, collecting international samples to find disease-associated variants

Learn more
Cellular & Molecular Biology Research
  • Cancer Sequencing Methods
  • Immuno-Oncology Research
  • Epigenetics
  • Chromosomal Abnormalities
  • Safety Data Sheets
  • FAQs
Clinical Cancer Research
  • Somatic Mutations
  • Germline Mutations
Training (Illumina University)
“Tripledemic” pathogen surveillance is critical
“Tripledemic” pathogen surveillance is critical

On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants

Read article

TBD

“Tripledemic” pathogen surveillance is critical
“Tripledemic” pathogen surveillance is critical

On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants

Read article

TBD

“Tripledemic” pathogen surveillance is critical
“Tripledemic” pathogen surveillance is critical

On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants

Read article

TBD

“Tripledemic” pathogen surveillance is critical
“Tripledemic” pathogen surveillance is critical

On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants

Read article

TBD

“Tripledemic” pathogen surveillance is critical
“Tripledemic” pathogen surveillance is critical

On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants

Read article
Oncology
  • Value of NGS in Oncology
  • Cancer Companion Diagnostics
  • Molecular Diagnostics
  • Medical Genetics Education
A new era for clinical labs
A new era for clinical labs

The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab

Learn more
  • TruSight Oncology 500 Product Family
  • Praxis Extended Ras Panel
  • In Vitro Diagnostic (IVD) Products
IVD Instruments
  • MiSeqDx Instrument
  • NextSeq 550Dx Instrument
A new era for clinical labs
A new era for clinical labs

The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab

Learn more
  • Library Prep & Array Kit Selector

More Tools

A new era for clinical labs
A new era for clinical labs

The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab

Learn more
Customer Interviews
  • Challenges and Potential of NGS in Oncology Testing
  • Predicting Cancer Risk
  • Breast Cancer Target Identification
Featured News
  • Promise of Liquid Biopsies
  • Partnerships Catalyze Patient Access to Genomic Testing
  • Patients with Challenging Cancers to Benefit from Sequencing
A new era for clinical labs
A new era for clinical labs

The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab

Learn more
Noninvasive Prenatal Testing
  • In-Lab Screening with NIPT
  • NIPT Sendout for Labs
NIPT Education for Labs
  • Cell-Free DNA Technology for NIPT
  • NIPT vs Traditional Aneuploidy Screening Methods
Medical Genetics Education

All Reproductive Health

A new era for clinical labs
A new era for clinical labs

The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab

Learn more
  • VeriSeq NIPT Solution
  • Infinium CytoSNP-850K BeadChip
  • NextSeq 550Dx Instrument

All Reproductive Health Products

A new era for clinical labs
A new era for clinical labs

The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab

Learn more
  • Library Prep & Array Kit Selector

More Tools

A new era for clinical labs
A new era for clinical labs

The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab

Learn more
Customer Interviews
  • SNP Array Identifies Inherited Genetic Disorder Contributing to IVF Failures
  • NIPT Delivers Sigh of Relief to Expectant Mother
  • Insights into Recurrent Pregnancy Loss
Featured News
  • Education is Key to Noninvasive Prenatal Testing
  • First NGS Agreement for NIPT
  • Study Takes a Look at Fetal Chromosomal Abnormalities

More News

A new era for clinical labs
A new era for clinical labs

The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab

Learn more
Genetic & Rare Diseases
  • Rare Disease Genomics
  • Cardiovascular Genomics
  • Rare Variant Data Analysis
  • Cystic Fibrosis Testing
  • iHope for Rare Pediatric Diseases
Announcing Illumina Complete Long Reads
Announcing Illumina Complete Long Reads

Illumina Complete Long Read technology enables both long and short reads on the same NovaSeq instrument

Learn more
  • TruSight Cystic Fibrosis
  • TruSight Software Suite
  • In Vitro Diagnostic (IVD) Products
IVD Instruments
  • Clinical Sequencing Services

All Genetic Health Products

Announcing Illumina Complete Long Reads
Announcing Illumina Complete Long Reads

Illumina Complete Long Read technology enables both long and short reads on the same NovaSeq instrument

Learn more
  • Library Prep & Array Kit Selector

More Tools

Announcing Illumina Complete Long Reads
Announcing Illumina Complete Long Reads

Illumina Complete Long Read technology enables both long and short reads on the same NovaSeq instrument

Learn more
Customer Interviews
  • Rare Disease Variants in Infants with Undiagnosed Disease
  • A Genetic Data Matchmaking Service for Researchers
  • Using NGS to Study Rare Undiagnosed Genetic Disease
Featured News
  • Progress for Patients with Rare and Undiagnosed Genetic Diseases
  • The Diagnostic Odyssey
  • The Story of Tree Baby

More News

Announcing Illumina Complete Long Reads
Announcing Illumina Complete Long Reads

Illumina Complete Long Read technology enables both long and short reads on the same NovaSeq instrument

Learn more
/Video Hub

lllumina NovaSeq X Series

NovaSeq X and NovaSeq X Plus Sequencing Systems provide high-throughput sequencing and productivity gains to enable sequencing of up to tens of thousands of genomes per year.

Using XLEAP-SBS chemistry, the NovaSeqX series is able to produce the highest level of data accuracy and performance and increased stability. These transformational sequencing economics will empower genomic scientists to realize projects previously thought out of reach. Users can have outstanding throughput and scalability without sacrificing flexible, streamlined, and easy-to-use workflows.

Watch NovaSeq X video

Illumina NovaSeq X Series

The limits of high-throughput sequencing redefined


View All Videos 
  • Featured Videos
  • Popular Videos
  • Recent Videos
  • Educational Videos
  • No Time to Stand Down: COVID and What's Next

    3663 views | 4 years ago

    Moderator: Phil Febbo, Illumina Panelists: Tulio de Oliveira, Nelson Mandela School of Medicine; Stacey Gabriel, The Broad Institute; Scott Gottlieb, New Enterprise Associates; Eric Topol, Scripps Research...

    Introducing Illumina Connected Analytics

    4103 views | 3 years ago

    Analyze, manage, aggregate, and explore data at scale with Illumina Connected Analytics, a secure genomics data platform to operationalize informatics and drive scientific insights. http://www.illumina.com/ConnectedAnalytics...

    Nobel to Nobel: Jennifer Doudna in conversation with Frances Arnold

    2555 views | 4 years ago

    Host: Frances Arnold, California Institute of Technology Spotlight Speaker: Jennifer Doudna, University of California Berkeley Description: Inside the groundbreaking journeys of two women in science,...

    Using Whole Genome Sequencing To Hunt For A Diagnosis in Rare Disease: The Future Is Now

    2689 views | 5 years ago

    What was once only a futuristic vision has become reality for patients and physicians seeking answers for a rare disease. Learn how whole genome sequencing can be deployed to hunt for a diagnosis and...

  • Introducing the new Illumina Viral Surveillance Panel V2

    716497 views | 10 months ago

    Subscribe to the Illumina video channel http://www.youtube.com/subscription_center?add_user=IlluminaInc A global genomics leader, Illumina provides comprehensive next-generation sequencing solutions...

    Illumina MiSeq™ i100 Series | Possibilities made simple

    62287 views | 7 months ago

    The MiSeq™ i100 Series sets the highest standard in benchtop sequencing with breakthrough simplicity, the fastest runtimes, and onboard DRAGEN™ analysis, all in one compact footprint. It enables users...

    The Illumina 3' Single Cell RNA Prep Workflow

    19104 views | 4 months ago

    Discover how the Illumina 3' Single Cell RNA Prep workflow makes single-cell sequencing simple, affordable, and microfluidics-free. With proven performance across diverse cell types and reliable, high-quality...

    Illumina MiSeq™ i100 Series | The next generation of benchtop sequencing systems

    10124 views | 7 months ago

    Meet the MiSeq™ i100 Series. The MiSeq i100 and MiSeq i100 Plus System sets the highest standard in benchtop sequencing. Breakthrough advancements in system design and XLEAP-SBS™ chemistry produce highly...

  • AGBT 2025: Illumina at the preeminent genome science and technology conference

    809 views | 2 months ago

    Illumina was the Gold Sponsor of the 25th annual Advances in Genome Biology and Technology (AGBT) Conference in Marco Island, Florida. Highlights include advancements in rare disease detection with...

    Fighting Drug-Resistant TB with Next-Generation Sequencing: A Crucial Tool to #EndTB2030

    223 views | 2 months ago

    With just 5 years remaining to achieve the goal of ending TB by 2030, we need to utilize better tools to combat drug-resistant TB (DR-TB). This animation highlights how Next-Generation Sequencing (NGS)...

    Streamlined and powerful spatial data analysis with Illumina Connected Multiomics

    407 views | 3 months ago

    Illumina Connected Multiomics enables analysis and visualization of transcript data, users can easily view their spatial data overlaid on tissue images, quickly filter and/or make selection in real...

    Introducing Illumina spatial technology

    1136 views | 3 months ago

    Illumina spatial technology will be a unique end-to-end spatial coding transcriptomics solution for use with Illumina high-throughput sequencing systems. Building on our expertise in flow cell development,...

  • Shining a light on the genomics of solar panels contamination

    850 views | 8 years ago

    Learn how scientists around the world are using next-generation sequencing to identify microbial species living on solar panels. Learn more at: http://www.illumina.com/applications/... Products: Illumina...

    The origin of fishfingers: CRISPR/Cas9 in the study of evolutionary and developmental biology

    820 views | 8 years ago

    CRISPR-Cas9 is a powerful study in the fields of developmental and evolutionary biology. Recent studies on fish, butterflies, and crustaceans are great examples on how this technique can be used to...

    Taking a Stab at Pierce’s Disease | Adventures in Genomics

    56317 views | 8 years ago

    Plants, like animals, depend on microbes to function to their fullest capacity. To understand more about plants, plant microbiomes, and plant disease, Jacques and Irene interviewed Caroline Roper from...

    Diversity In Our Diets | Adventures in Genomics

    51866 views | 9 years ago

    Complex diseases have increased dramatically over the last few decades. Many of these are associated with abnormalities in composition of the microbiome, but the cause/effect relationship still remains...

illumina logo
For Research Use Only

Not for use in diagnostic procedures (except as specifically noted).

Not for import or sale to the Australian general public.

Innovative technologies

At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. As a global company that places high value on collaborative interactions, rapid delivery of solutions, and providing the highest level of quality, we strive to meet this challenge. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics.

Illumina Korea
14F iM Investment & Securities building
66 Yeoidaero Yeoungdeungpo-gu
Seoul Korea 07325
  • 02-740-5300 (tel)
  • 02-786-8368 (fax)
  • customercare@illumina.com

판매 약관 | Tax Reg: 105-87-87282 | Retailer Reg: 2019-서울영등포-2018 | Host: https://www.illumina.com | Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A.

All trademarks are the property of Illumina, Inc. or their respective owners.
For specific trademark information, see www1.tst-web.illumina.com/company/legal.html.

Careers Contact Us
Illumina on Twitter Illumina on Facebook Illumina on LinkedIn Illumina on Instagram 

© 2025 Illumina, Inc. All rights reserved.