High-throughput sequencing

Bringing valuable insights to light with the latest advances in Illumina high-throughput next-generation sequencing technology

Advantages of high-throughput sequencing

The latest innovations in Illumina high-throughput next-generation sequencing technology power advanced applications to generate dramatically more data for more impactful insights. Increasingly, scientists are leveraging the advantages of advanced next-generation sequencing (NGS) applications with our simplified, cost-efficient high-throughput sequencing workflows.

Key highlights

Improve statistical power

Increase statistical power using larger sample sizes for more impactful conclusions

Access previously missed information

See the full breadth of variation with whole-genome or whole-transcriptome sequencing

Get multidimensional insights

Uncover multidimensional insights and generate a single readout across DNA, RNA, and protein.

Increase analytical resolution

Transition to high-resolution approaches, including single-cell sequencing and spatial analyses for insights into complex tissues

High-throughput sequencing technology innovations

The latest advances in Illumina sequencing have enabled high-throughput sequencing applications, bringing insights that were unimaginable even a few years ago and removing barriers with every technological innovation.

Scalable

Get an unparalleled breadth of targets. Create multidimensional insights with optimized indexing strategies. Illumina high-throughput sequencing provides a single robust readout for multiple -omes.

Cost-effective

Amplify your insights. Cast a wider net with larger sample sizes. Cost-effective high-throughput sequencing opens up your options for sequencing applications and allows additional insights for a more comprehensive view of your sample.

Technology innovation roadmap

Explore the technologies pushing the frontiers of NGS-based research with simpler workflows, greater discovery power, and new possibilities.

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Discover more with multiomics

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.

Popular high-throughput sequencing methods

Achieve impactful insights and accelerate your lab’s work with these methods. Explore a wide variety of high-throughput NGS research methods and their key benefits.

Genomics

Epigenetics

Transcriptomics

Proteomics

High-throughput sequencers

Dream big. The NovaSeq X Series can make it happen.

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 52 billion single reads per dual flow cell run. Advanced chemistry, optics, and informatics provide exceptional accuracy and speed that enable transformative economics for groundbreaking discoveries.

Drive discoveries with the NovaSeq 6000 System

A tried-and-true high-throughput instrument with improved economics and an output of up to 6 Tb and 20 billion 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.

Run diverse applications on the NextSeq 2000 System

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 52 billion single reads per dual flow cell run. Advanced chemistry, optics, and informatics provide exceptional accuracy and speed that enable transformative economics for groundbreaking discoveries.

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High-throughput NGS data analysis

Perform ultra-rapid, user-friendly data analysis

Illumina DRAGEN secondary analysis

This software provides ultra-rapid secondary genomic analysis with highly accurate results, diverse applications, and frequent updates. DRAGEN software can process NGS data for an entire human genome at 30× coverage in about 25 minutes.

Aggregate, explore, and share large volumes of data

Illumina BioInsight Platform Core

This software is a secure, cloud-based platform for managing genomic data and analysis. Automate pipelines, run DRAGEN and custom workflows, and scale from pilot studies to population-level programs.

High-throughput lab setup resources

Streamline your lab operations

Discover how the NovaSeq X Series provides a new standard in operational simplicity, driving breakthroughs and maximizing productivity.

Bioinformatics pipeline setup

Find out how to simplify the informatics infrastructure and data analysis pipeline setup process and access more data for more insights.

Multiplex sequencing

Understand how to pool and sequence large numbers of NGS libraries simultaneously during a single run.

Supporting genome center growth

Read how the Deakin Genomics Centre uses Illumina NGS for high-throughput sequencing projects to lower sequencing costs and provide a faster sequencing data turnaround time.

Identifying breast cancer targets

Learn how the 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.

Automate your library prep

Learn how 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.

Featured webinars

Scale sequencing with greater efficiency

Watch how a core lab uses the latest NovaSeq X Series innovations to streamline high-throughput sequencing workflows, optimize output, and rapidly deliver high-quality data.

FAQ

Consider your research goals, application, sample number, read length, sequencing depth, and required data output. Planning these factors together can help you select an appropriate sequencing strategy and make efficient use of available sequencing capacity. Illumina provides NGS experimental design and planning resources to help evaluate considerations such as read length, coverage, and sequencing quality.

Sequencing throughput is the total amount of sequencing data a system can generate, while sequencing depth describes how many times a particular base or region is sequenced. Higher throughput can support more samples, greater sequencing depth, or a combination of both, depending on the study design. Learn more about sequencing depth.

High-throughput sequencing can support increasing sample numbers while providing the sequencing capacity needed for data-intensive applications. Multiplex sequencing can further increase sample throughput by allowing uniquely indexed libraries to be pooled and sequenced together in the same run.

Maintaining data quality as studies scale starts with careful experimental design and consistent workflows across library preparation, sequencing, and data analysis. Evaluating factors such as sequencing quality scores, read length, and coverage can help researchers design experiments that meet their data quality requirements. Illumina provides experimental planning guidance covering each of these considerations

Moving to high-throughput sequencing may be appropriate when using increasing sample volumes, greater sequencing depth, or data-intensive applications begin to exceed the practical capacity of a benchtop workflow. Consider current project requirements and anticipated growth when evaluating the throughput and scalability your lab needs. Compare Illumina sequencing platforms to find a system that aligns with your research needs.

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Related resources

Instrument buying options

Interested in the latest high-throughput sequencer? Don’t let your budget hold you back. Explore different buying options to find which best fits your needs.

Speak to a specialist

Talk to an expert about implementing high-throughput sequencing to do more in your lab.