The latest innovations in Illumina high-throughput sequencing technology power advanced sequencing applications to generate dramatically more data for more impactful insights. Increasingly, scientists are leveraging the advantages of advanced sequencing applications with our simplified, cost-efficient high-throughput sequencing workflows.
Increased statistical power from larger sample sizes for more impactful conclusions.
See the full breadth of variation with whole-genome or whole-transcriptome sequencing.
Multidimensional insights with sequencing provide a single readout from multiple -omes across DNA, RNA, and protein.
Transition to high-resolution approaches, including single-cell sequencing and spatial analyses for insights into complex tissues.
Get an unparalleled breadth of targets. Create multi-dimensional insights with optimized indexing strategies. Illumina high-throughput sequencing provides a single robust readout for multiple -omes.
Amplify your insights. Cast a wider net with larger sample sizes. Cost-effective high-throughput sequencing opens up your options to do high-intensity sequencing applications and gain additional insights for a more comprehensive view of your sample.
Combine genomic data with data from other modalities such as transcriptomics, epigenetics, and proteomics to measure gene expression, gene activation, and protein levels. High-throughput omics profiling studies enable a more comprehensive understanding of molecular changes contributing to normal development, cellular response, and disease.
Explore popular methods and their key benefit.
See the entire genome
Gain deeper insights into complex regions of the genome
Detect exonic variants
Explore the methylome
Map chromatin accessibility across the genome
Simultaneously evaluate gene expression and surface protein expression levels at single-cell resolution
Get full transcriptome data
Unleash your ambitions with the NovaSeq X and NovaSeq X Plus Sequencing Systems, our most powerful and most sustainable sequencers yet. The ultra-high-throughput NovaSeq X Plus System delivers up to 16 Tb output and 52B single reads per dual flow cell run. Advanced chemistry, optics, and informatics provide exceptional accuracy and speed that enable transformative economics for groundbreaking discoveries.View System View Reagents
A tried-and-true high-throughput instrument with improved economics and an output of up to 6 Tb and 20B single reads in < 2 days. Unlock a full spectrum of genetic variation and biological function with high-throughput sequencing on the NovaSeq 6000 system. Advances in reagents support a vast breadth of targets and complex indexing strategies.View System View Reagents
NextSeq 2000 System is redesigned from the ground up to maximize future proofing, offering sequencing power for high-throughput applications. With adjustible output and scalability for evolving needs and larger studies, the system and reagents make a vast variety of data-rich multiomics applications accessible, including whole-exome, and single-cell sequencing.
The platform for ultra-rapid secondary genomic analysis with highly accurate results, diverse applications, and frequent updates. DRAGEN can process NGS data for an entire human genome at 30x coverage in about 25 minutes.Learn More
This comprehensive cloud-based data management and analysis software platform empowers researchers to manage, analyze, and interpret large volumes of multiomics data in a secure, scalable, and flexible environment. The platform is built for high-volume operations limited by data silos and a lack of bioinformatics and data science tools.Learn More
The NovaSeq X Series provides a new standard in operational simplicity, driving breakthroughs and maximizing productivity.
Find out how to simplify the informatics infrastructure and data analysis pipeline setup process and access more data for more insights.
Pool and sequence large numbers of NGS libraries simultaneously during a single run.
The Deakin Genomics Centre uses Illumina NGS for high-throughput sequencing projects to lower sequencing costs and provide a faster sequencing data turnaround time.
Garvan Institute scientists use Illumina high-throughput NGS to sequence more than a million breast cancer cells to help create a comprehensive cellular atlas of breast cancer.
These walk-away automation methods for Illumina kits eliminate the need to develop your own method and can help you reduce hands-on time and minimize errors.
Learn how to take multiplex proteomics to the next level and discover protein biomarkers using Illumina sequencers.
Interested in trading in your HiSeq System for the latest high-throughput sequencer with more discovery power? You may be eligible to trade in your existing instrument for a new NovaSeq 6000 System.
Explore Illumina high-throughput sequencing options. Get additional training, find software, plan experiments, purchase, and get support.