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

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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.

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RESEARCH

 
Cancer
 
Microbiology
 
Agrigenomics
 
Complex Disease
 
Cellular and Molecular Biology


CLINICAL

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

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CUSTOMER INTERVIEW


USING ANALYTICS TO IMPROVE CANCER DIAGNOSIS

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

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CUSTOMER VIDEOS


ADVANCING CANCER RESEARCH WITH MULTIOMICS

Learn how researchers at the Ontario Institute for Cancer Research and United
Health Network are linking the causes and consequences of complex...

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ADVANCING CANCER RESEARCH WITH MULTIOMICS


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CORE TECHNOLOGY


SEQUENCING

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CORE TECHNOLOGY


MICROARRAYS

Analyze genetic variation on any scale

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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.

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TRUSIGHT ONCOLOGY 500 SELECTION TOOL

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POPULAR TOOLS

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 * MYILLUMINA CUSTOMER DASHBOARD
   
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 * LIBRARY PREP AND ARRAY KIT SELECTOR
   
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 * CUSTOM PROTOCOL SELECTOR
   
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 * DESIGNSTUDIO CUSTOM ASSAY DESIGNER
   
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--------------------------------------------------------------------------------

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FEATURED NEWS


BRIDGING THE DIAGNOSIS GAP FOR CANADA’S INDIGENOUS CHILDREN

The Silent Genomes Project is building a first-of-its-kind variant library for
First Nations, Inuit, and Métis populations

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   Press Releases
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   In the News

Date Title Jul 18, 2023 The Alliance for Genomic Discovery announces founding
biopharma members: AbbVie, Amgen, AstraZeneca, Bayer, and Merck Jul 11, 2023
Illumina DRAGEN™ 4.2 delivers most accurate and comprehensive coverage of the
genome, powering greater applications and discovery Jun 11, 2023 Illumina
announces CEO transition plan

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Date Publication Title Jun 3, 2023 Fierce Biotech ASCO: Illumina's oncology exec
on the need to 'democratize genomic profiling in cancer' Jun 1, 2023 Science
Hundreds of new primate genomes offer window into human health—and our past Jun
1, 2023 The Washington Post New AI tool searches genetic haystacks to find
disease-causing variants

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EMPLOYEE STORY

FOLLOW SUZANNE THROUGH HER TYPICAL DAY AS A BIOINFORMATICS SCIENTIST

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FOLLOW SUZANNE THROUGH HER TYPICAL DAY AS A BIOINFORMATICS SCIENTIST

 




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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.

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