Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.Learn More
This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths.
Comprehensive sequencing research panels targeting disease-associated regions of the exome with high analytical sensitivity and specificity.
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information.
Targeting 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types including blood, bone marrow, and formalin-fixed, paraffin-embedded (FFPE) tissue.
These sequencing reagent kits offer a simplified workflow and improved data quality compared to the prior v1 kit version.
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
This software provides a user-friendly on-instrument solution for creating sequencing runs, monitoring run status, and analyzing data. It includes a Somatic Variant Module and Germline Variant Module.Learn More
DesignStudio is a web-based assay design tool to help researchers design and order custom sequencing probes, or create custom genotyping array assays.
Setting up and running sequencing experiments is easy with software tools designed for Illumina sequencing systems.
Simplify your bioinformatics with an economical and powerful computing environment to manage, analyze, and share data.
BaseSpace Cohort Analyzer allows you to integrate and analyze subject and genomic data together using innovative visualization and analysis tools.
BaseSpace Correlation Engine mines over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research.
BaseSpace Variant Interpreter enables genetic labs to rapidly identify biologically significant variants from human genomic data.
Illumina services and support begins when the NextSeq 550Dx System is delivered. Illumina scientists and engineers assist with NGS system installation and setup and train laboratory personnel. In addition to on-site support, training courses are available to bring laboratory personnel quickly up to speed.
Illumina scientists are available 24/7 globally to answer questions every step of the way, enabling researchers to focus on making the next breakthrough discovery.
In addition to the 1-year basic service warranty included with system purchase, Illumina offers maintenance, repair, and qualification solutions.
Get high-quality results on Illumina technology even faster with instructor-led, hands-on courses and web-based training options.
Illumina provides consulting services that connect an experienced Illumina team direct to the laboratory to jump-start successful sequencing workflow implementation.
* Contact your Illumina representative for more information about IVD development partnerships
The NextSeq 550Dx instrument is intended for targeted sequencing of DNA libraries from human genomic DNA extracted from peripheral whole blood or formalin-fixed, paraffin-embedded (FFPE) tissue, when used for in vitro diagnostic (IVD) assays performed on the instrument. The NextSeq 550Dx instrument is not intended for whole genome or de novo sequencing. The NextSeq 550Dx instrument is to be used with registered and listed, cleared or approved, IVD reagents and analytical software.
The NextSeq 550Dx instrument is intended for sequencing of DNA libraries when used with in vitro diagnostic (IVD) assays performed on the instrument. The NextSeq 550Dx instrument is to be used with specific registered, certified or approved IVD reagents and analytical software.