Library preparation is a required sequencing step. Use our selection tool to determine the best library prep kit for your needs based on your application, method, species, and more.
If you currently own a HiSeq, NextSeq 500/550/Dx, or a MiSeq System, you may be eligible to trade in your existing instrument for a NextSeq 1000 or NextSeq 2000 System. Restrictions apply. Contact a sales representative using the form below to learn more about eligibility.
In this video, an Illumina Field Applications Scientist discusses what to expect during the pre-installation, shipping, and delivery stages. We’ll highlight important steps in the process and introduce you to available resources.
Indexed Sequencing Overview Documentation
NextSeq 1000 and 2000 Denature and Dilute Libraries Guide Documentation
Security and Networking Documentation
RFID Reader Compliance Guide Documentation
NextSeq 1000/2000 Sequencing System Guide Documentation
NextSeq 1000/2000 Sequencing System Documentation
NextSeq 1000 and 2000 Custom Primers Guide Documentation
NextSeq 1000 and NextSeq 2000 Sequencing Systems Safety and Compliance Guide Documentation
NextSeq 1000 and 2000 Sequencing System Site Prep Guide Documentation
Custom Protocol Selector
Generates customized, end-to-end instructions
All NextSeq 1000/2000 Sequencing System Support Resources Support
A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing.
A simple, scalable, cost-effective, rapid single-day solution for analyzing the coding transcriptome leveraging as little as 25 ng input of standard (non-degraded) RNA.
NextSeq 1000/2000 reagent kits contain a reagent cartridge, flow cell, and resuspension buffer. Multiple flow cell configurations offer adjustable output based on project needs.
Achieve rapid, targeted interrogation of an expansive number of target genes with exceptional capture efficiency and coverage uniformity.
Highly sensitive detection and characterization of common respiratory viruses, including COVID-19 strains, with comprehensive, rapid target enrichment sequencing.
Rapid library preparation from a broad range of sample types for studying the coding and non-coding transcriptome with unparalleled study flexibility.
