Coming soon. This new configuration will provide 100 M reads and 10 Gb of data and is ideally situated for bulk and single counting applications such as RNA-Seq, ATAC-Seq, ChIP-Seq, and more!
Coming soon. This new configuration will provide 100 M reads and 60 Gb of data and brings longer read capabilities with more output for Immune Repertoire, Shotgun Metagenomics and more!
Coming soon. This new configuration will provide 300 M reads and 180Gb of data and brings longer read capabilities with more output for Immune Repertoire, Shotgun Metagenomics and more!
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 Options
A fast, integrated workflow for a wide range of applications encompassing custom panels, fixed panels, and whole-exome enrichment.
Data management and simplified bioinformatics for labs getting started and for rapidly scaling next-generation sequencing (NGS) operations.
iCredits are the currency used to purchase Illumina genomic data storage and analysis options.
This kit combines next-generation sequencing with epigenetic insights to accelerate biomarker discovery and understand methylation’s role in gene regulation.
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.
Simple, cost-effective chromatin immunoprecipitation sequencing (ChIP-Seq) DNA library preparation, with master mixes and robust multiplex capabilities.
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 More
ICA is a secure genomic data platform to operationalize informatics and drive scientific insights. Build, version, deploy, and run analytical pipelines at scale while maintaining data privacy, security, and compliance with ICA.
BaseSpace Sequence Hub offers NGS data analysis apps for common Illumina sequencing methods.
These tools accelerate coronavirus detection and identification, simplify sample tracking, and help scientists contribute to public databases, free of charge.
BaseSpace Variant Interpreter allows scientists to rapidly identify biologically significant variants from human genomic data.
BaseSpace Correlation Engine mines over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research.
DesignStudio is a web-based assay design tool to help researchers design and order custom sequencing probes, or create custom genotyping array assays.
Phosphorus uses the DRAGEN Bio-IT Platform to perform genomics data analysis onsite and at an accessible price point.Read Interview
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 More
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.Learn More