IVD development and testing on the NextSeq 550Dx System*
The TruSeq Custom Amplicon Kit Dx and the NextSeq 550Dx High Output Reagent Kit are IVD reagents and consumables that work together to provide a flexible toolkit for developing and performing diagnostic tests on the NextSeq 550Dx.
Featured Clinical Research Products
TruSight Tumor 170
Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.
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TruSeq DNA Exome
This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths.
TruSight One Sequencing Panels
Comprehensive sequencing research panels targeting disease-associated regions of the exome with high analytical sensitivity and specificity.
TruSeq Stranded mRNA
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information.
TruSight RNA Pan-Cancer
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.
NextSeq 500/550 v2.5 Kits
These sequencing reagent kits offer increased stability and robustness over the v2 kit version.
TruSight Oncology 500
Assay targeting multiple variant types, including microsatellite instability (MSI) and tumor mutational burden (TMB).
Illumina Advantage Products
View a list of currently available off-the-shelf Illumina Advantage products tailored to the needs of clinical laboratories.
View KitsSoftware and Informatics Solutions
Local Run Manager (for diagnostic mode only)
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 MoreBaseSpace Sequence Hub
Data management and simplified bioinformatics for labs getting started and for rapidly scaling next-generation sequencing (NGS) operations.
Correlation Engine
Correlation Engine is an interactive omics knowledgebase that puts private omics data in biological context with highly curated public data.
BaseSpace Variant Interpreter
BaseSpace Variant Interpreter allows scientists to rapidly identify biologically significant variants from human genomic data.
Instrument Services
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.
Illumina Product Care
In addition to the 1-year basic service warranty included with system purchase, Illumina offers maintenance, repair, and qualification solutions.
Illumina Training
Get high-quality results on Illumina technology even faster with instructor-led, hands-on courses and web-based training options.
* Contact your Illumina representative for more information about IVD development partnerships
Intended Use for the NextSeq 550Dx
United States:
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.
European Union:
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.