www.illumina.com Open in urlscan Pro
99.80.73.249  Public Scan

Form analysis
0 forms found in the DOM

Text Content

Products Learn Company Support
Products
 * Instruments
 * Kits & Reagents
 * Selection Tools
 * Software & Analysis
 * Services
 * Popular Products

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

All Instruments

DREAM BIG. NOVASEQ X CAN MAKE IT HAPPEN.

Learn More
Kits & Reagents
 * Library Preparation Kits
 * Sequencing Reagents
 * Microarray Kits
 * Clinical Research Products
 * IVD Products

All Kits & Reagents

ANNOUNCING ILLUMINA COMPLETE LONG READS

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

Learn More
Selection Tools
 * Library Prep & Array Kit Selector
 * Gene Panel & Array Finder
 * Sequencer Comparison Tool
 * DesignStudio Custom Assay Designer
 * TruSight Oncology 500 Product Selector

All Selection & Planning Tools

TRUSIGHT ONCOLOGY 500 SELECTION TOOL

Filter by batch size, system, software, and more. Compare and cart products.

Find the Right Kit
Software & Analysis
 * BaseSpace Sequence Hub
 * DRAGEN Secondary Analysis
 * Illumina Connected Analytics
 * Emedgene
 * Illumina Connected Insights
 * Clarity LIMS
 * Correlation Engine
 * Microarray Software

All Software & Informatics Products

ILLUMINA CONNECTED INSIGHTS

Enable insights and variant interpretation for diverse genomic testing
applications at scale

Learn More
Services
 * Sequencing Services
 * Microarray Services
 * Proactive Instrument Monitoring
 * Instrument Services & Training

All Services

ILLUMINA PROACTIVE INSTRUMENT PERFORMANCE SERVICE

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

Learn More
Popular Products
 * 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

NEW NEXTSEQ 1000/2000 P1 AND P2 600-CYCLE KITS

New configurations will bring longer read capabilities with more output for
immune repertoire, shotgun metagenomics and more

Order Now
Learn
 * Areas of Interest
 * Techniques
 * Technology
 * Illumina Research & Innovation
 * Training
 * Publications
 * Data Analysis & Informatics

See All Learning Options
Areas of Interest
Research Applications
 * Cancer Research
 * Microbiology
 * Agrigenomics
 * Complex Disease Genomics
 * Cellular & Molecular Biology

Clinical Applications
 * Reproductive Health
 * Oncology
 * Genetic & Rare Diseases

All Areas

COMPREHENSIVE COVERAGE OF CARDIAC GENES

Understanding cardiovascular diseases through genomic sequencing

Learn More
Techniques
Sequencing
 * DNA Sequencing
 * RNA Sequencing
 * High-Throughput Sequencing
 * Library Preparation

Microarrays
Popular Genomics Applications
 * Genotyping
 * Gene Expression Analysis
 * Epigenetics
 * Genome Editing
 * Multiomics

All Techniques

COMPREHENSIVE COVERAGE OF CARDIAC GENES

Understanding cardiovascular diseases through genomic sequencing

Learn More
Technology
NGS for Beginners
Our Technologies
 * Next-Generation Sequencing
 * Long-Read Sequencing
 * Microarray Technology

Sequencing Method Explorer

All Technologies

COMPREHENSIVE COVERAGE OF CARDIAC GENES

Understanding cardiovascular diseases through genomic sequencing

Learn More
Illumina Research & Innovation
Genomics Research Hub
 * Genomics Articles
 * Illumina Publications
 * Open-Source Bioinformatics Tools

COMPREHENSIVE COVERAGE OF CARDIAC GENES

Understanding cardiovascular diseases through genomic sequencing

Learn More
Training
Illumina Resources & Tools
NGS for Beginners
Genomics Education
 * Illumina NGS & Array Training
 * Educational Webinars
 * Support Webinars & Online Training
 * Videos
 * Podcasts

Medical Genetics

All Training

COMPREHENSIVE COVERAGE OF CARDIAC GENES

Understanding cardiovascular diseases through genomic sequencing

Learn More
Publications
Peer-Reviewed Publications
 * Illumina Publications
 * Publication Summaries

Customer Stories
 * iCommunity Interviews
 * Customer Videos
 * More Stories

COMPREHENSIVE COVERAGE OF CARDIAC GENES

Understanding cardiovascular diseases through genomic sequencing

Learn More
Data Analysis & Informatics
Infrastructure & Pipeline Setup
Sequencing Data Analysis
Biological Data Interpretation

All Informatics Education

COMPREHENSIVE COVERAGE OF CARDIAC GENES

Understanding cardiovascular diseases through genomic sequencing

Learn More
Company
 * About Us
 * News & Events
 * Careers
 * Corporate Social Responsibility
 * Investor Info
 * Doing Business With Us
 * Legal

See All Company Info
About Us
 * Office Locations
 * Management Team
 * Board of Directors
 * Ethics Advisory Board
 * Fact Sheet
 * Corporate Social Responsibility
 * iHope Philanthropic Sequencing
 * Governance & Code of Conduct

More About Us

25 YEARS OF INNOVATION

Our mission is to improve human health by unlocking the power of the genome

Learn More
News & Events
News Center
 * Feature Articles
 * Perspectives Blog
 * Press Releases
 * Illumina in the News
 * Illumina Images

Events & Webinars
 * Illumina Genomics Forum

25 YEARS OF INNOVATION

Our mission is to improve human health by unlocking the power of the genome

Learn More
Careers
 * Overview
 * Search Jobs
 * Career Tracks
 * Employee Stories
 * Illumina Locations & Benefits

More Career Info

25 YEARS OF INNOVATION

Our mission is to improve human health by unlocking the power of the genome

Learn More
Corporate Social Responsibility
 * Overview
 * Accelerate Access to Genomics
 * Empower Our Communities
 * Integrate Sustainability
 * Nurture Our People
 * Advance Diversity, Equity, & Inclusion
 * Operate Responsibly
 * ESG Hub

25 YEARS OF INNOVATION

Our mission is to improve human health by unlocking the power of the genome

Learn More
Investor Info
 * Overview
 * Shareholder Events
 * Financial Information
 * Stock Information
 * Corporate Governance

All Investor Information

25 YEARS OF INNOVATION

Our mission is to improve human health by unlocking the power of the genome

Learn More
Doing Business With Us
 * MyIllumina Customer Dashboard
 * Financial Solutions
 * Instrument Buying Options
 * Illumina Accelerator Startup Funding
 * Distributors
 * Suppliers
 * Partnerships
 * Contact Us

More Business Solutions

25 YEARS OF INNOVATION

Our mission is to improve human health by unlocking the power of the genome

Learn More
Legal
 * Terms & Conditions
 * Report a Compliance Issue
 * Privacy
 * Governance & Code of Conduct

All Legal Information

25 YEARS OF INNOVATION

Our mission is to improve human health by unlocking the power of the genome

Learn More
Support
 * Product Support
 * Documents and Training
 * Tools
 * Services
 * Additional Resources
 * Contact & Medical Info

View All Support
Product Support
 * Instrument Support
 * Library Prep Kit Support
 * Microarray Support
 * Software Support

ILLUMINA DRAGEN SECONDARY ANALYSIS V4.0

Get instructions for using DRAGEN Secondary Analysis v4.0

Learn More
Documents and Training
 * Documentation
 * Technical Bulletins
 * Illumina Adapter Sequences
 * Support Webinars & Online Training
 * Instructor-Led & Other Training

ILLUMINA DRAGEN SECONDARY ANALYSIS V4.0

Get instructions for using DRAGEN Secondary Analysis v4.0

Learn More
Tools
 * 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

Get instructions for using DRAGEN Secondary Analysis v4.0

Learn More
Services
 * Proactive Instrument Monitoring
 * Qualification Services

All Product Support Services

ILLUMINA DRAGEN SECONDARY ANALYSIS V4.0

Get instructions for using DRAGEN Secondary Analysis v4.0

Learn More
Additional Resources
 * Certificates (CofC, CofA) and Master Lot Sheets
 * Safety Data Sheets
 * Share Desktop

ILLUMINA DRAGEN SECONDARY ANALYSIS V4.0

Get instructions for using DRAGEN Secondary Analysis v4.0

Learn More
Contact Us
 * Distributors
 * Suppliers
 * Medical Information & Resources
 * All Contact Info

ILLUMINA DRAGEN SECONDARY ANALYSIS V4.0

Get instructions for using DRAGEN Secondary Analysis v4.0

Learn More








25 YEARS OF INNOVATION


OUR MISSION IS TO IMPROVE HUMAN HEALTH BY UNLOCKING THE POWER OF THE GENOME. WE
BELIEVE THAT, TOGETHER, WE CAN USE GENOMICS TO BUILD A STRONGER WORLD FOR THE
GREATER GOOD.

Learn More



RESEARCH

 
Cancer
 
Microbiology
 
Agrigenomics
 
Complex Disease
 
Cellular and Molecular Biology


CLINICAL

 
Reproductive Health
 
Genetic & Rare Diseases
 
Oncology
Explore Areas of Interest 
 * Cancer Research
 * Microbiology
 * Agrigenomics
 * Complex Disease
 * Cellular and Molecular Biology
 * Reproductive Health
 * Genetic & Rare Diseases
 * Clinical Oncology




CUSTOMER INTERVIEW


IDENTIFYING BREAST CANCER TARGETS USING NGS

The Breast Cancer Atlas Project is sequencing more than a million breast cancer
cells with the NovaSeq 6000 System.

Read Article


CUSTOMER INTERVIEW


USING ANALYTICS TO IMPROVE CANCER DIAGNOSIS

Developing and automating workflows for analyzing, processing, and sharing
genomic data among researchers and clinicians.

Read Article


CUSTOMER VIDEOS


TRANSFORMING ONCOLOGY WITH GENOMICS

Researchers from the Ontario Institute for Cancer Research and United Health
Network share how knowing more about cancer biology through genomic...

View Video
x

TRANSFORMING ONCOLOGY WITH GENOMICS


See More Interviews See More Videos

 


CORE TECHNOLOGY


SEQUENCING

See what sequencing can do for you

Learn MoreCompare Sequencers
 


CORE TECHNOLOGY


MICROARRAYS

Analyze genetic variation on any scale

Learn MoreCompare Array Scanners
See All Instruments

 


ANNOUNCING ILLUMINA COMPLETE LONG READS

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

Learn More


DREAM BIG. NOVASEQ X CAN MAKE IT HAPPEN.



Learn More


LIMITED TIME OFFER ON RIBO-ZERO PLUS KIT

Save on the Ribo-Zero Plus Microbiome rRNA Depletion Kit, restrictions apply.

Order Now



EDUCATION AND WEBINARS

Learn about the latest genomics discoveries by Illumina scientists, or find
webinars and free courses to get the most out of your experiments

Explore Discoveries View Webinars View Courses

 

FEATURED TOOL


TRUSIGHT ONCOLOGY 500 SELECTION TOOL

Filter by batch size, system, software, and more. Compare and cart products.

Find the Right Kit


POPULAR TOOLS

--------------------------------------------------------------------------------


 * MYILLUMINA CUSTOMER DASHBOARD
   
   Sign In or Learn More


 * LIBRARY PREP AND ARRAY KIT SELECTOR
   
   Launch Tool


 * BASESPACE SEQUENCE HUB
   
   Sign In or Learn More


 * CUSTOM PROTOCOL SELECTOR
   
   Build Protocol


 * DESIGNSTUDIO CUSTOM ASSAY DESIGNER
   
   Sign In or Learn More

--------------------------------------------------------------------------------

See More Tools


FEATURED NEWS


ADDRESSING THE GENOMICS EDUCATION GAP

With limited space in the curricula for genomics, residents and physicians are
turning to other sources for training

Read Article
 * 
   Press Releases
 * 
   In the News

Date Title Jun 11, 2023 Illumina announces CEO transition plan Jun 5, 2023
Illumina releases 2022 Corporate Social Responsibility Report Jun 2, 2023
Illumina's Board of Directors elects two experienced Independent Directors to
Board

View All Press Releases



Date Publication Title Apr 25, 2023 ITVX Blood test for lung cancer could speed
up diagnosis in Wales as trial launched Apr 11, 2023 Inside Precision Medicine
Illumina, Henry Ford Health Partner to Study Impact of CGP on Cardiovascular
Disease Mar 31, 2023 HealthAffairs Thinking Differently About Multicancer Early
Detection Screening Tests

View All Illumina News


 

EMPLOYEE STORY

FOLLOW SUZANNE THROUGH HER TYPICAL DAY AS A BIOINFORMATICS SCIENTIST

View Video View More Stories
Search Jobs
×

FOLLOW SUZANNE THROUGH HER TYPICAL DAY AS A BIOINFORMATICS SCIENTIST

 




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

Hi 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 www.illumina.com/company/legal.html.

Cookie Settings Cookie Settings Privacy Policy
Careers Contact Us
 

© 2023 Illumina, Inc. All rights reserved.


Feedback

Accept cookies to provide feedback.





SEE MORE RELEVANT CONTENT. CHOOSE YOUR PRIMARY AREA OF INTEREST:

×
Cancer Research
Microbiology
Agrigenomics
Complex Disease
Clinical Oncology
Reproductive Health
Genetic & Rare Diseases
Remove my preference
×






COOKIE PREFERENCES

Illumina, Inc. and its subdivisions use cookies to tailor website content and
provide you with an optimal user experience. Select "Accept All Cookies” to get
the most out of this site, or visit our Cookie Settings and allow specific types
of cookies. Read our Cookie Policy to learn more.

Accept Essential Cookies Only Accept All Cookies