Featured NextSeq 1000 & NextSeq 2000 Products & Services
New Products
NextSeq 1000/2000 P1 Reagents (100Cycles)
This new configuration provides 100M reads and 10 Gb of data and is ideally suited for bulk and single counting applications such as RNA-Seq, ATAC-Seq, ChIP-Seq, and more!
NextSeq1000/2000 P1 Reagents (600Cycles)
This new configuration provides 100M reads and 60 Gb of data and brings longer read capabilities with more output for Immune Repertoire, Shotgun Metagenomics, and more!
NextSeq 1000/2000 P2 300M Reagents (600Cycles)
This new configuration provides 300M reads and 180 Gb of data and brings longer read capabilities with more output for Immune Repertoire, Shotgun Metagenomics, and more!
Featured Products
NextSeq 1000 and NextSeq 2000 Reagents
With a wide range of output from 100M to 1200M reads, NextSeq 1000 and 2000 reagents have you covered—whether it's pilot projects or lower depth samples on the P1 flow cell, mid-range studies on P2 flow cell, and higher output projects with reduced per-sample costs on the P3 flow cells.
View Reagent Kit OptionsLibrary Preparation
Find library preparation solutions for a broad range of DNA, RNA, and epigenetic sequencing methods. Explore automation options and technical tips.
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Software and Informatics Solutions
Illumina DRAGEN Bio-IT Platform License Now Included
The NextSeq 1000 and NextSeq 2000 Sequencing Systems come equipped with the power of onboard DRAGEN to provide accurate and fast secondary analysis at no additional cost. Seamlessly integrate sequencing and secondary analysis in run setup, simplify the workflow, reduce the turnaround time, and extend the value of the data generated by the NextSeq 1000 and NextSeq 2000.
Learn MoreBaseSpace Sequence Hub Apps
BaseSpace Sequence Hub offers NGS data analysis apps for common Illumina sequencing methods.
Coronavirus Software
These tools accelerate coronavirus detection and identification, simplify sample tracking, and help scientists contribute to public databases, free of charge.
BaseSpace Variant Interpreter
BaseSpace Variant Interpreter allows scientists to rapidly identify biologically significant variants from human genomic data.
BaseSpace Correlation Engine
BaseSpace Correlation Engine mines over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research.
DesignStudio Custom Assay Designer
DesignStudio is a web-based assay design tool to help researchers design and order custom sequencing probes, or create custom genotyping array assays.
Bringing Bioinformatics In-House Reduces Costs and Decreases Turnaround Time
Phosphorus uses the DRAGEN Bio-IT Platform to perform genomics data analysis onsite and at an accessible price point.
Read InterviewTrusted, reliable benchtop sequencing
Find out how Illumina commits to upholding a proven track record of benchtop sequencing solutions that empower scientists to advance and accelerate their research.
Learn MoreInstrument Services & Training
Access a full suite of services designed to maximize performance and productivity. From instrument service plans and training to qualification services and free instrument performance services – we are here to support all of your customer needs.
Learn MoreIllumina Resources & Tools
This central hub offers education and assistance for your workflow, from start to finish. Learn about our technology, design your project, access selection tools, find software to glean valuable insights from your data, then purchase what you need and get support.
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