NextSeq™ 1000 and NextSeq™ 2000 Sequencing Systems
Expansive application breadth and operational simplicity with proven performance
Receive your quote directly from the manufacturer.
The NextSeq 1000 and NextSeq 2000 Systems offer the certainity of a field-tested solution and reliable sequencing partner. Take advantage of a large ecosystem of applications, protocols, and informatics built in collaboration with thousands of researchers and thought leaders across the globe.
For Research Use Only
Not for use in diagnostic procedures (except as specifically noted).
Brochures
Illumina Sequencing Systems: Redefine possible
In this brochure, Illumina highlights its portfolio of next-generation sequencing systems, designed to empower researchers and clinicians across genetic disease, reproductive health, oncology, microbiology, agriculture, and more. Discover how Illumina’s comprehensive suite of platforms provides the tools and innovations needed to generate high-quality genomic data, enabling ground-breaking insights and supporting evolving research and clinical applications.
NextSeq 1000 and NextSeq 2000 Sequencing Systems
In this brochure, Illumina highlights the NextSeq™ 1000 and NextSeq™ 2000 Sequencing Systems, benchtop platforms designed to expand next-generation sequencing capabilities for diverse research applications. Learn more about high-performance sequencing by synthesis chemistry, integrated onboard informatics, scalable throughput, and consistent data quality, which enables labs to efficiently tackle applications from small to large batches in oncology, microbiome research, and beyond.
DRAGEN Bio-IT Platform onboard the NextSeq 1000 and NextSeq 2000 systems
In this data sheet, Illumina describes how the DRAGEN™ Bio-IT Platform is integrated into the NextSeq™ 1000 System and NextSeq 2000 System to provide fast and accurate secondary analysis for next-generation sequencing workflows. Discover how onboard DRAGEN software enables streamlined data processing during sequencing run setup, reducing the need for additional computing infrastructure while supporting a wide range of NGS applications, including exome, transcriptome, targeted sequencing, metagenomics, and single-cell analysis.
