Find kits, reagents, and accessories compatible with the NovaSeq X and NovaSeq X Plus Systems.
32 Results
Manage runs, analyze, store, and share sequencing data in BaseSpace Sequence Hub. Find applications, subscription options, and documentation.
A highly customizable laboratory information management system that allows genomics labs to track samples and manage workflows efficiently and securely.
An interactive omics knowledge base that analyzes private omics data with highly curated public data to help researchers put their data into biological context.
Highly accurate, high-performance full workflow solution for comprehensive human WGS with long-read data from NovaSeq platforms.
A cost-effective, flexible, targeted long-read solution to address challenging-to-map regions of the human genome.
A study design tool that combines private data with public data sets for rapidly building and exploring cohorts.
Operationalize informatics and drive scientific insights with Illumina Connected Analytics. Contact us for information on pricing, subscriptions, and more.
Targeted custom enrichment panels, providing simple and efficient solutions for multiple targeted sequencing applications.
An efficient, fast, and integrated library preparation workflow that yields highly accurate data for sensitive sequencing applications.
A complete targeted resequencing solution for a wide range of applications, with fast integrated workflow and options for custom and fixed enrichment panels.
A high-performance, fast, and reliable human whole-exome sequencing solution that includes a comprehensive, up-to-date exome enrichment panel.
A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.
Maximize genomic insights with DRAGEN secondary analysis, learn about the latest updates, read FAQs, and find product support.
Predesigned, optimized panel to provide enhanced coverage of challenging-to-map regions within protein-coding genes using Illumina Complete Long Reads with Enrichment library prep kit. Analyzed in combination with a required ≥ 30× standard short-read whole genome.
Illumina Protein Prep combines trusted Illumina chemistry, SOMAmer technology, and DRAGEN data analysis for a comprehensive, automated NGS-based proteomics solution.
Streamlined RNA-Seq solution for clear and comprehensive analysis across the coding and non-coding transcriptome with exceptional study flexibility.
A rapid, cost-effective workflow for accurate, unbiased detection of the protein-coding transcriptome with precise measurement of strand information.
Unique dual (UD) indexes enable preparation of high-quality libraries that can be multiplexed for increased throughput and cost-saving benefits.
Verify instrument installation and operation, and obtain a digital, audit-ready document from certified Illumina engineers to help meet regulatory guidelines.
Nextera DNA Indexes enable preparation of high-quality libraries that can be multiplexed for increased throughput.
Sequencing systems with up to 16 Tb output per run on the dual flow cell NovaSeq X Plus System or up to 8 Tb on the single flow cell NovaSeq X System.
Whole-genome sequencing delivers a comprehensive view, ideal for discovery applications. Newer genome sequencers perform WGS more rapidly than ever.
Whole-exome sequencing is used to investigate protein-coding regions of the genome to uncover genetic influences on disease and population health.