DRAGEN secondary analysis
Get accurate, comprehensive, and highly efficient bioinformatics with multiple deployment options, applications, and pipelines to meet your research needs.
Expand biological discovery with the power of high-throughput multiomics
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The NovaSeq X Series delivers the scalable sequencing power and flexibility to support a broad range of methods for interrogating the genome, epigenome, transcriptome, and proteome. Engineered to output data with the highest integrity, the NovaSeq X Series makes even the most data-intensive research accessible with industry leading speed and throughput.
We have been combining samples from multiple projects and users on the same large run on the NovaSeq X Series with a 10B or 25B flow cell.
This 25B flow cell is a great example of the diverse library types we are able to sequence in an efficient way.
The time is now for multiomics to address complex biological questions. Watch the video to discover how scientists are gaining an advantage in their sample-to-discovery journey through the power of the NovaSeq X Series.
Technical note spotlight
Learn how you can achieve high-throughput, genome-scale Perturb-Seq experiments with NovaSeq X 25B flow cells. In this technical note, in collaboration with Single Cell Discoveries, we demonstrate a large-scale CRISPR interference workflow.
A broad portfolio of high-throughput Illumina and third-party solutions to interrogate the genome, epigenome, trancriptome, and proteome.
The NovaSeq X and NovaSeq X Plus Sequencing Systems provide exceptional throughput and accuracy for your data-intensive applications at scale.
Experience the power of our secure and flexible bioinformatics platform, designed to operationalize informatics workflows and drive groundbreaking scientific insights.
The NovaSeq X Series makes multiomics accessible to enable discoveries that were previously out of reach. Explore products and reagents, with supporting application notes, resources, and relevant analysis solutions to interpret results for omics workflows below.
By studying the genome, researchers can use information about the structure, function, and sequence of DNA to better understand its role in health and disease.
A rapid and flexible workflow for sensitive whole-genome sequencing.
A fast, robust, and flexible workflow for a wide range of DNA input types.
The fastest and most flexible targeted DNA sequencing solution from Illumina.
A highly sensitive library preparation solution to detect low-abundance mutations from cell-free DNA samples. Learn more in our data sheet.
Explore products for Illumina Complete Long Read sequencing.
Illumina offers a comprehensive portfolio of software solutions to analyze omic data and lead to novel insights. Explore informatic solutions capable of scaling to production-level systems such as the NovaSeq X Series to streamline data to insight with efficiency and ease.
Get accurate, comprehensive, and highly efficient bioinformatics with multiple deployment options, applications, and pipelines to meet your research needs.
Integrates with Illumina sequencing systems with an intuitive interface for streamlined run setups and monitoring. Enjoy intuitive push-button secondary analysis and data sharing within a secure cloud ecosystem with expandable storage for growing laboratory needs.
A secure, scalable, bioinformatics platform that enables you to manage, analyze, and interpret large volumes of multiomic data.
Partek Flow bioinformatics software provides a visual user interface, robust statistical algorithms, information-rich visualizations, and cutting-edge genomic tools that enable researchers of all skill levels to confidently perform data analysis.
An interactive omics knowledgebase that puts private omics data in biological context with highly curated public data.
Watch this Illumina Connected Analytics workflow demo specific to Cohorts for multiomic cancer analysis.
Read this update on the introduction of innovative pipelines for DRAGEN, including single-cell ATAC-Seq and single-cell multiomics (RNA-Seq and ATAC-Seq).
Learn how sequencing runs with 10x Genomics libraries can now be directly set up on the Run Planner. The Run Planner tool guides you through the steps needed for preparing your sequencing run, such as specifying sample and index information, read length and analysis options.
Learn how to combine RNA and protein data, statistically assess relationships using correlation between gene and protein molecules, and explore differences between cell types using differential analysis comparisons for biological interpretation.
Learn how researchers harness Illumina Correlation Engine to accelerate discovery and publications.
Application note spotlight
In this application note, learn how the ability to measure and visualize 80 surface proteins across 1000 single cells per sample—utilizing the Pixelator pipeline and analysis package—can enhance your understanding of immune cell behavior in cancer.
The power of multiomics eBook
See how you can use multiomics to better connect genotype to phenotype and obtain a full cellular readout not found through single omics approaches.
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Multiomic sequencing with the NovaSeq X Series eBook
Learn how you can perform broader, deeper sequencing with the NovaSeq X Series and take on omics projects that were previously out of reach.
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Gene expression and regulation bioinformatics eBook
Learn more about the NGS data analysis workflow and get an overview of software solutions available for analyzing gene expression and regulation data.
Your email address is never shared with third parties.
Single-cell sequencing eBook
Explore every step of the single-cell sequencing workflow and learn valuable insights to ensure experimental success.
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Reach out for information about our products and services, or get answers to questions about our technology.
Your email address is never shared with third parties.
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