Speed, scale and discovery power with the NovaSeq X Series
Unlock deeper insights for more meaningful outcomes
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With the NovaSeq X Series, you can take on projects that were previously out of reach. Sequence both broader and deeper at scale than ever before. The lower cost per Gb, higher-throughput, and fast, streamlined operational workflows allow you to sequence more samples and analyze data more easily than ever before.
The NovaSeq X Series and 1.5B, 5B, 10B, and 25B flow cells enable users to leverage budgets to perform sequencing studies of greater scale and depth.
* $200 USD genome on NovaSeq X Series is delivered at list price on the 25B flow cell (sequencing consumables only), assuming 100 Gb/genome.
Increased discovery power will come from larger studies, deeper sequencing to identify rare genetic events, broader sequencing methods, and incorporating multiple -omes for a comprehensive view of cellular activity. Learn how the NovaSeq X Series makes it easy to transition to high-throughput and expand your application reach.
Your email address is never shared with third parties.
The NovaSeq X Series allows you to sequence more deeply to analyze rare variants, or scale up any application to include more samples. By leveraging the NovaSeq X Series 5B, 10B, and 25B flow cells, you can work with bigger cohorts, faster than ever with the highest level of confidence.
Perform ctDNA sequencing to detect rare variants and low-frequency signals in liquid biopsy research samples.
Access the contributions of individual cells in complex tissues by profiling up to millions of single cells in parallel, under more conditions, and at genome-scale.
Add statistical power and sequence 2.5× more samples by transitioning from the NovaSeq 6000 S4 flow cell to the NovaSeq X 25B flow cell.
Affordably analyze up to 64 human whole genomes per flow cell to power rare disease research.
Efficiently identify coding variants for larger cohort groups with the ability to sequence 436 exomes per NovaSeq X 25B flow cell.
Whole-genome sequencing was performed on the NovaSeq X Plus System with 25B flow cells and on the NovaSeq 6000 System with S4 flow cells using the same total project budget of $500,000 USD. The analysis is based on sequencing >120 Gb of data per sample to achieve 30× genome coverage.
Sequence 2.5× more cells in half the timea with the 25B flow cell on the NovaSeq X Plus System. By leveraging the NovaSeq X Series 1.5B, 5B, 10B and 25B flow cells, you can work with bigger cohorts, faster than ever with the highest level of confidence.
| NovaSeq X flow cell type |  |
 |
 |
 |
|---|---|---|---|---|
| No. of single cells sequenced per runb | ~120,000 | ~400,000 | ~800,000 | ~2M |
| Run timec | ~17 hr | ~18 hr | ~18 hr | ~48 hr |
It's now easier to perform a broad range of multiomics studies and add an additional dimension of information with the NovaSeq X Series. Answer the most complex questions in genomics by getting the most information out of every single sample.
By combining multiple methods for deeper insights, you can think bigger with your projects and drive utility. Here are some of the top methods that are validated for the NovaSeq X Series and commonly combined for multiomics studies.
| Common multiomics combinations and benefits | How NovaSeq X helps | Popular methods |
|---|---|---|
| Genomics + transcriptomics Measure the functional consequences of genetic variation to annotate and prioritize variants associated with disease |
Automated, push-button onboard secondary analysis for WGS, WES, and RNA-Seq that can run in parallel |
|
| Genomics + epigenetics Reveal patterns of gene regulation and how they connect with the genotypes underlying disease, especially in noncoding regions |
Automated onboard independent lane loading to easily sequence multiple omes on the same flow cell |
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| Transcriptomics + epigenetics Directly measure the ties between gene regulation and gene expression, instead of trying to infer those connections |
Seamlessly connected to full suite of DRAGEN secondary analysis pipelines in the cloud |
Multiomics at a lower cost than one “ome” alone: sequencing both whole exomes and whole transcriptomes on the NovaSeq X Series 25B flow cell is more cost effective than running whole-exome sequencing alone on previous platforms.
Implementing sequencing workflows is faster and easier than ever before with the NovaSeq X Series. There are fewer touch points and steps, from run planning to sequencing and analysis. Accelerate your sequencing with the streamlined workflow and easily manage large amounts of data with DRAGEN onboard the NovaSeq X Series.
Illumina Run Manager
*Connected Insights available in select countries
High-accuracy sequencing with the NovaSeq X Series
XLEAP-SBS chemistry delivers exceptional data quality for high-throughput genomics, and technology advances make the NovaSeq X Series our most powerful and cost-effective sequencing systems yet.
RNA-Seq on the NovaSeq X Series
Empower your research using RNA-Seq with the NovaSeq X Series. Learn about the streamlined RNA-to-results workflow that combines power, speed, and flexibility for high-throughput transcriptome analysis.
TruSight Oncology ctDNA v2 on the NovaSeq X Series
This application note compares the performance of the NovaSeq X Series and NovaSeq 6000 System using the TruSight Oncology ctDNA v2 CGP assay. Results demonstrate the same high level of performance with significantly reduced run times when using the NovaSeq X Series.
There is nothing more important than innovation at Illumina. It’s how we move the field forward and it’s part of everything we do. See how every detail has been redesigned in the NovaSeq X Series to elevate usability, maximize productivity, and minimize turnaround to make the most of your precious samples.
Earlham Institute and WorldFish: Changing the world with the NovaSeq X Plus System
Feeding the world’s growing population requires big advances in sustainable aquaculture. In this video, three scientists describe how the Illumina NovaSeq X Series is helping make these advances possible.
OICR & Princess Margaret: Changing the world with the NovaSeq X Plus System
The Ontario Institute for Cancer Research (OICR) is working to better understand tumor biology through the use of genomics. Learn how OICR uses the NovaSeq X Plus System to accelerate projects, like those with Dr Stephanie Lheureux at Princess Margaret Cancer Centre.
Talk to an expert about adopting broader and deeper sequencing approaches in your lab.
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