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Welcome to Immense Discovery Power
Welcome to Immense Discovery Power

NovaSeq 6000 Sequencing System is by far our most powerful instrument, designed to adapt to your needs.

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NextSeq 1000/2000 Reagents
NextSeq 1000/2000 Reagents

P1 reagents are now available for NextSeq 1000/NextSeq 2000 Systems, offering added flexibility to meet your project's needs

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Library Prep Kit Selector: Infinium OmniExpressExome-8 Kit
Library Prep Kit Selector: Infinium OmniExpressExome-8 Kit

A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing

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Illumina DRAGEN Bio-IT Platform
Illumina DRAGEN Bio-IT Platform

DRAGEN v3.9 release now available with multi-cloud support, accuracy improvements and more

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Sequencing Services
Sequencing Services

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NovaSeq 6000 Reagent Kits v1.5
NovaSeq 6000 Reagent Kits v1.5

Improved Q30 score, support for UMIs, extended shelf life, and support for Illumina DNA PCR-Free Library Prep

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Bringing Greater Insights, Answers, and Breakthroughs to Light
Bringing Greater Insights, Answers, and Breakthroughs to Light

See what is possible through the latest advances in high-throughput sequencing technology

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Bringing Greater Insights, Answers, and Breakthroughs to Light
Bringing Greater Insights, Answers, and Breakthroughs to Light

See what is possible through the latest advances in high-throughput sequencing technology

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Bringing Greater Insights, Answers, and Breakthroughs to Light
Bringing Greater Insights, Answers, and Breakthroughs to Light

See what is possible through the latest advances in high-throughput sequencing technology

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Bringing Greater Insights, Answers, and Breakthroughs to Light
Bringing Greater Insights, Answers, and Breakthroughs to Light

See what is possible through the latest advances in high-throughput sequencing technology

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Bringing Greater Insights, Answers, and Breakthroughs to Light
Bringing Greater Insights, Answers, and Breakthroughs to Light

See what is possible through the latest advances in high-throughput sequencing technology

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Bringing Greater Insights, Answers, and Breakthroughs to Light
Bringing Greater Insights, Answers, and Breakthroughs to Light

See what is possible through the latest advances in high-throughput sequencing technology

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Bringing Greater Insights, Answers, and Breakthroughs to Light
Bringing Greater Insights, Answers, and Breakthroughs to Light

See what is possible through the latest advances in high-throughput sequencing technology

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Sequencing to Save the Lemurs
Sequencing to Save the Lemurs

Illumina and the San Diego Zoo Wildlife Alliance try to preserve the species with the help of genomic data

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Sequencing to Save the Lemurs
Sequencing to Save the Lemurs

Illumina and the San Diego Zoo Wildlife Alliance try to preserve the species with the help of genomic data

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Sequencing to Save the Lemurs
Sequencing to Save the Lemurs

Illumina and the San Diego Zoo Wildlife Alliance try to preserve the species with the help of genomic data

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Sequencing to Save the Lemurs
Sequencing to Save the Lemurs

Illumina and the San Diego Zoo Wildlife Alliance try to preserve the species with the help of genomic data

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Sequencing to Save the Lemurs
Sequencing to Save the Lemurs

Illumina and the San Diego Zoo Wildlife Alliance try to preserve the species with the help of genomic data

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Sequencing to Save the Lemurs
Sequencing to Save the Lemurs

Illumina and the San Diego Zoo Wildlife Alliance try to preserve the species with the help of genomic data

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MiSeqDx Windows 10 Update
MiSeqDx Windows 10 Update

Upgrade your MiSeqDx instrument from Windows 7 to Windows 10

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MiSeqDx Windows 10 Update
MiSeqDx Windows 10 Update

Upgrade your MiSeqDx instrument from Windows 7 to Windows 10

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MiSeqDx Windows 10 Update
MiSeqDx Windows 10 Update

Upgrade your MiSeqDx instrument from Windows 7 to Windows 10

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MiSeqDx Windows 10 Update
MiSeqDx Windows 10 Update

Upgrade your MiSeqDx instrument from Windows 7 to Windows 10

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MiSeqDx Windows 10 Update
MiSeqDx Windows 10 Update

Upgrade your MiSeqDx instrument from Windows 7 to Windows 10

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MiSeqDx Windows 10 Update
MiSeqDx Windows 10 Update

Upgrade your MiSeqDx instrument from Windows 7 to Windows 10

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Multiomics Offers a Holistic View of Human Health
Multiomics Offers a Holistic View of Human Health

Multiomics methods can better connect genotype to phenotype

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  • TruSight Oncology 500 Product Family
  • AmpliSeq for Illumina Cancer Hotspot Panel v2
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Multiomics Offers a Holistic View of Human Health
Multiomics Offers a Holistic View of Human Health

Multiomics methods can better connect genotype to phenotype

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  • Library Prep & Array Kit Selector
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Multiomics Offers a Holistic View of Human Health
Multiomics Offers a Holistic View of Human Health

Multiomics methods can better connect genotype to phenotype

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  • BaseSpace Sequence Hub Apps
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Multiomics Offers a Holistic View of Human Health
Multiomics Offers a Holistic View of Human Health

Multiomics methods can better connect genotype to phenotype

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Multiomics Offers a Holistic View of Human Health
Multiomics Offers a Holistic View of Human Health

Multiomics methods can better connect genotype to phenotype

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Microbial Sequencing Methods
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Surveillance of SARS-CoV-2 Variants
Surveillance of SARS-CoV-2 Variants

Learn about methods for SARS-CoV-2 surveillance, including requirements, workflow, and analysis

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  • Illumina COVIDSeq Test
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Surveillance of SARS-CoV-2 Variants
Surveillance of SARS-CoV-2 Variants

Learn about methods for SARS-CoV-2 surveillance, including requirements, workflow, and analysis

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  • Library Prep & Array Kit Selector
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Surveillance of SARS-CoV-2 Variants
Surveillance of SARS-CoV-2 Variants

Learn about methods for SARS-CoV-2 surveillance, including requirements, workflow, and analysis

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  • BaseSpace Sequence Hub Apps
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Surveillance of SARS-CoV-2 Variants
Surveillance of SARS-CoV-2 Variants

Learn about methods for SARS-CoV-2 surveillance, including requirements, workflow, and analysis

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Surveillance of SARS-CoV-2 Variants
Surveillance of SARS-CoV-2 Variants

Learn about methods for SARS-CoV-2 surveillance, including requirements, workflow, and analysis

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SNP Arrays for Dual Hybridization of Wheat and Barley
SNP Arrays for Dual Hybridization of Wheat and Barley

Array-based SNP genotyping platforms have low genotype error rates compared to genotyping-by-sequencing

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  • Illumina DNA Prep
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SNP Arrays for Dual Hybridization of Wheat and Barley
SNP Arrays for Dual Hybridization of Wheat and Barley

Array-based SNP genotyping platforms have low genotype error rates compared to genotyping-by-sequencing

Watch Webinar
  • Library Prep & Array Kit Selector
  • Sequencer Comparison Tool
  • Gene Panel & Array Finder
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SNP Arrays for Dual Hybridization of Wheat and Barley
SNP Arrays for Dual Hybridization of Wheat and Barley

Array-based SNP genotyping platforms have low genotype error rates compared to genotyping-by-sequencing

Watch Webinar
  • BaseSpace Sequence Hub Apps
  • GenomeStudio Software

All Informatics Products

SNP Arrays for Dual Hybridization of Wheat and Barley
SNP Arrays for Dual Hybridization of Wheat and Barley

Array-based SNP genotyping platforms have low genotype error rates compared to genotyping-by-sequencing

Watch Webinar
Customer Interviews
  • Ecosystem Monitoring with eDNA
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Featured News
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SNP Arrays for Dual Hybridization of Wheat and Barley
SNP Arrays for Dual Hybridization of Wheat and Barley

Array-based SNP genotyping platforms have low genotype error rates compared to genotyping-by-sequencing

Watch Webinar
Complex Disease Genomics
  • Disease Association Studies
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Illumina Training
Benefits of Gene Expression Profiling with RNA-Seq
Benefits of Gene Expression Profiling with RNA-Seq

Explore the advantages of NGS for analysis of gene expression, gene regulation, and methylation

Download eBook
  • 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

Benefits of Gene Expression Profiling with RNA-Seq
Benefits of Gene Expression Profiling with RNA-Seq

Explore the advantages of NGS for analysis of gene expression, gene regulation, and methylation

Download eBook
  • Library Prep & Array Kit Selector
  • Gene Panel & Array Finder
  • Sequencing Coverage Calculator
  • Custom Protocol Selector
  • Disease to Gene Finder

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Benefits of Gene Expression Profiling with RNA-Seq
Benefits of Gene Expression Profiling with RNA-Seq

Explore the advantages of NGS for analysis of gene expression, gene regulation, and methylation

Download eBook
  • BaseSpace Sequence Hub Apps
  • BaseSpace Variant Interpreter
  • BaseSpace Correlation Engine
  • Microarray Software

All Informatics Products

Benefits of Gene Expression Profiling with RNA-Seq
Benefits of Gene Expression Profiling with RNA-Seq

Explore the advantages of NGS for analysis of gene expression, gene regulation, and methylation

Download eBook
Customer Interviews
  • Polygenic Risk Scores
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  • Rare Disease Variants in Infants
Featured News
  • Every Diagnosis Matters
  • The Story of Tree Baby
  • Mysteries of Rare & Undiagnosed Diseases

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Benefits of Gene Expression Profiling with RNA-Seq
Benefits of Gene Expression Profiling with RNA-Seq

Explore the advantages of NGS for analysis of gene expression, gene regulation, and methylation

Download eBook
Cellular & Molecular Biology Research
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Surveillance of SARS-CoV-2 Variants
Surveillance of SARS-CoV-2 Variants

Learn about methods for SARS-CoV-2 surveillance, including requirements, workflow, and analysis

Watch Webinar

TBD

Surveillance of SARS-CoV-2 Variants
Surveillance of SARS-CoV-2 Variants

Learn about methods for SARS-CoV-2 surveillance, including requirements, workflow, and analysis

Watch Webinar

TBD

Surveillance of SARS-CoV-2 Variants
Surveillance of SARS-CoV-2 Variants

Learn about methods for SARS-CoV-2 surveillance, including requirements, workflow, and analysis

Watch Webinar

TBD

Surveillance of SARS-CoV-2 Variants
Surveillance of SARS-CoV-2 Variants

Learn about methods for SARS-CoV-2 surveillance, including requirements, workflow, and analysis

Watch Webinar

TBD

Surveillance of SARS-CoV-2 Variants
Surveillance of SARS-CoV-2 Variants

Learn about methods for SARS-CoV-2 surveillance, including requirements, workflow, and analysis

Watch Webinar
Oncology
  • Value of NGS in Oncology
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Bringing Greater Insights, Answers, and Breakthroughs to Light
Bringing Greater Insights, Answers, and Breakthroughs to Light

See what is possible through the latest advances in high-throughput sequencing technology

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  • TruSight Oncology 500 Product Family
  • Praxis Extended Ras Panel
  • In Vitro Diagnostic (IVD) Products
IVD Instruments
  • MiSeqDx Instrument
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Bringing Greater Insights, Answers, and Breakthroughs to Light
Bringing Greater Insights, Answers, and Breakthroughs to Light

See what is possible through the latest advances in high-throughput sequencing technology

Learn More
  • Library Prep & Array Kit Selector
  • Sequencer Comparison Tool
  • Disease to Gene Finder

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Bringing Greater Insights, Answers, and Breakthroughs to Light
Bringing Greater Insights, Answers, and Breakthroughs to Light

See what is possible through the latest advances in high-throughput sequencing technology

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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
Bringing Greater Insights, Answers, and Breakthroughs to Light
Bringing Greater Insights, Answers, and Breakthroughs to Light

See what is possible through the latest advances in high-throughput sequencing technology

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

Impact of NIPT on Prenatal Screening for Chromosomal Anomalies
Impact of NIPT on Prenatal Screening for Chromosomal Anomalies

Prof. Dr. Bernd Eiben discusses his experience with VeriSeq NIPT Solution v2

Read Article
  • VeriSeq NIPT Solution
  • Infinium CytoSNP-850K BeadChip
  • NextSeq 550Dx Instrument

All Reproductive Health Products

Impact of NIPT on Prenatal Screening for Chromosomal Anomalies
Impact of NIPT on Prenatal Screening for Chromosomal Anomalies

Prof. Dr. Bernd Eiben discusses his experience with VeriSeq NIPT Solution v2

Read Article
  • Library Prep & Array Kit Selector
  • Sequencer Comparison Tool

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Impact of NIPT on Prenatal Screening for Chromosomal Anomalies
Impact of NIPT on Prenatal Screening for Chromosomal Anomalies

Prof. Dr. Bernd Eiben discusses his experience with VeriSeq NIPT Solution v2

Read Article
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

Impact of NIPT on Prenatal Screening for Chromosomal Anomalies
Impact of NIPT on Prenatal Screening for Chromosomal Anomalies

Prof. Dr. Bernd Eiben discusses his experience with VeriSeq NIPT Solution v2

Read Article
Genetic & Rare Diseases
  • Rare Disease Genomics
  • Cardiovascular Genomics
  • Rare Variant Data Analysis
  • Cystic Fibrosis Testing
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China’s Rare Disease Community: Coordinating Research and Efforts
China’s Rare Disease Community: Coordinating Research and Efforts

Illumina supports the release of a landmark consensus on whole-genome sequencing in the diagnosis of genetic diseases in newborns

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

All Genetic Health Products

China’s Rare Disease Community: Coordinating Research and Efforts
China’s Rare Disease Community: Coordinating Research and Efforts

Illumina supports the release of a landmark consensus on whole-genome sequencing in the diagnosis of genetic diseases in newborns

View Video
  • Library Prep & Array Kit Selector
  • Sequencer Comparison Tool
  • Disease to Gene Finder

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China’s Rare Disease Community: Coordinating Research and Efforts
China’s Rare Disease Community: Coordinating Research and Efforts

Illumina supports the release of a landmark consensus on whole-genome sequencing in the diagnosis of genetic diseases in newborns

View Video
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

China’s Rare Disease Community: Coordinating Research and Efforts
China’s Rare Disease Community: Coordinating Research and Efforts

Illumina supports the release of a landmark consensus on whole-genome sequencing in the diagnosis of genetic diseases in newborns

View Video
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