Tailored to suit your research
Compatible products for your workflow. Kits, automation protocols, software solutions, and services for the NovaSeq 6000 System.
Ready-to-use, cartridge-based reagents with multiple flow cell configurations create a combination of scalable output and proven performance for reliable high-throughput sequencing.
An efficient, fast, and integrated library preparation workflow that yields highly accurate data for sensitive sequencing applications.
A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.
Reagent kits for the NovaSeq 6000 System consisting of ready-to-use pre-filled reagent cartridges and flow cells.
A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.
Offers a 90-min workflow to prepare DNA libraries for small genomes, PCR amplicons, plasmids, and cDNA sequencing, with a low DNA input requirement.
Streamlined RNA-Seq solution for clear and comprehensive analysis across the coding and non-coding transcriptome with exceptional study flexibility.
High-throughput library prep automation
Automation methods for many of our library prep assays are available from leading automation companies. Our partners offer a range of automation platforms to address your lab's throughput needs.
Laboratory information management systems (LIMS)
Use a LIMS to automate workflows, track reagents and lots, integrate instruments, and manage samples and associated information.
The Illumina genomics cloud-computing environment for NGS data analysis and management.
Illumina DRAGEN secondary analysis
Accurate, comprehensive, and efficient secondary analysis of next-generation sequencing (NGS) data.
bcl2fastq and bcl2fastq2 Conversion Software
Documentation, product files, FAQs, and other support resources for the bcl2fastq and bcl2fastq2 Conversion Software.
Set up and run sequencing experiments easily with software tools designed for Illumina sequencing systems.
An interactive omics knowledge base that analyzes private omics data with highly curated public data to help researchers put their data into biological context.
Our variant annotation and analysis software tools can help researchers extract and report biological insights from large volumes of genomic data.
A highly customizable laboratory information management system that allows genomics labs to track samples and manage workflows efficiently and securely.