Illumina DNA Prep with Enrichment
A complete targeted resequencing solution for a wide range of applications, with fast integrated workflow and options for custom and fixed enrichment panels.
Kits, services, and software solutions
Find the right sequencing kits, software, and services to support your NextSeq 1000 and NextSeq 2000 workflows and applications
The NextSeq 2000 P4 flow cell delivers 1.8 billion single-end reads per run, maximizing batching and powering data-rich projects like exome sequencing, multiomics, single-cell, and spatial analysis.
The NextSeq 1000 and NextSeq 2000 Systems offer broad platform utility with the flexibility to expand applications and scale efficiently. With 14 kit configurations and read lengths from 1 × 50 bp to 2 × 300 bp, you’ll have the reagents you need for your benchtop studies.
The NextSeq 1000 and NextSeq 2000 Systems offer access to DRAGEN secondary analysis, an onboard, local, and cloud-based software with flexible features for robust analysis.
These systems come pre-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 Systems.
DRAGEN software onboard the NextSeq 1000 and NextSeq 2000 Systems streamlines workflows with accurate secondary analysis. High quality variant calls and efficient DRAGEN pipeline algorithms ensure simplified operation while reducing reliance on external informatics experts.
BaseSpace Sequence Hub is a direct extension of Illumina instruments. Encrypted data flow from the instrument into BaseSpace Sequence Hub, enabling easy management and analysis with a curated set of analysis applications.
Operationalize bioinformatics workflows with sequencer integration, automatic analysis of customizable workflows, or out-of-the-box DRAGEN pipelines.
Find out how Illumina commits to upholding a proven track record of benchtop sequencing solutions that empower scientists to advance and accelerate their research.
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.
Find library preparation solutions for a broad range of DNA, RNA, and epigenetic sequencing methods. Explore automation options and technical tips.
Get up and running quickly with a rental or leasing program designed to work with your budget.
Your email address is never shared with third parties.