Access the latest technology today with flexible financing for instruments and reagents
All Kits & Reagents
Improved Q30 score, support for UMIs, extended shelf life, and support for Illumina DNA PCR-Free Library Prep
All Selection & Planning Tools
Compare NGS systems and find the one that's right for your needs
All Software & Informatics Products
Integrated secondary analysis onboard the NovaSeq X System simplifies operations, accelerates the sequencing workflow turnaround
Our instrument performance service helps reduce unplanned downtime and minimize instrument requalification
All Popular Products
Deeper studies, more samples, more modalities. The NovaSeq X and 25B flow cell make ultra-high depth multiomics more accessible.
A new algorithm trained by natural selection can pinpoint disease-causing variants in humans
All Informatics Education
More About Us
Empower the next generation of scientists and engineers through educational opportunities and resources
More Career Info
All Investor Information
More Business Solutions
All Legal Information
Get instructions for using DRAGEN Secondary Analysis v4.2
All Support Tools
All Product Support Services
Improved sensitivity using lower cfDNA input, a faster turnaround time, and a more streamlined workflow
All Cancer Research Products
All Microbial Genomics Research
On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants
All Microbial Genomics Products
All Informatics Products
Sport sailors can use these environmental DNA collection kits even at full speed
All Agrigenomics Products
The institution is taking its research global, collecting international samples to find disease-associated variants
All Complex Disease Research Products
The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab
All Reproductive Health
All Reproductive Health Products
Illumina Complete Long Read technology enables both long and short reads on the same NovaSeq instrument
All Genetic Health Products
Delivers a range of ready-to-use and custom panels for simple, flexible targeted resequencing that provides high-quality data you can trust.
Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
A fast, user-friendly workflow for a wide range of target enrichment applications encompassing custom panels, fixed panels, and whole-exome sequencing.
Perform targeted genotyping on large numbers of samples. Scale up to more than 1 million samples per year.
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Affordable, fast, and accessible sequencing power for targeted or small genome sequencing in any lab.
Perform high-throughput, cost-effective genotyping for quality control, tracking, and stratification applications, including biobanking.
Purchase the TruSight Oncology 500 assay for the first time and receive an exclusive limited time offer.
Whole-genome sequencing library prep kits for small genomes (e.g. bacterial and viral genomes), amplicons, and plasmids.
Rapid library preparation from a broad range of sample types for studying the coding and non-coding transcriptome with unparalleled study flexibility.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
A simple, scalable, cost-effective, rapid single-day solution for analyzing the coding transcriptome leveraging as little as 25 ng input of standard (non-degraded) RNA.
This array offers an optimal and comprehensive set of both common and rare SNP content for diverse world populations.
Interrogate over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
Optimized chemistry to increase cluster density and read length, and improve sequencing quality scores, compared to earlier MiSeq reagent kit versions.
These sequencing reagent kits offer increased stability and robustness over the prior v2 kit version.