Solutions for the NovaSeq X Series
Kits, automation options, and software tools
The power of XLEAP-SBS chemistry combined with flexible, efficient, sustainable workflows for transformational genomics at scale.
An efficient, fast, and integrated library preparation workflow that yields highly accurate data for sensitive sequencing applications.
A complete targeted resequencing solution for a wide range of applications, with fast integrated workflow and options for custom and fixed enrichment panels.
Streamlined RNA-Seq solution for clear and comprehensive analysis across the coding and non-coding transcriptome with exceptional study flexibility.
A fast, integrated workflow for producing enriched and indexed sequencing libraries from a broad range of sample types and RNA input quantities.
Reagent kits for the NovaSeq X Series include a reagent cartridge, buffer cartridge, flow cell, lyo insert, pre-load buffer, and library tube strip.
Simple, cost-effective chromatin immunoprecipitation sequencing (ChIP-Seq) DNA library preparation, with master mixes and robust multiplex capabilities.
To aid with adopting automation, methods for many of our library prep assays are available from the leading automation companies. Our partners offer a range of automation platforms to address your lab's throughput needs.
Laboratory information management systems (LIMS)
By using a LIMS, your lab can automate workflows, track reagents and lots, integrate instruments, and manage samples and associated information.
Accurate, comprehensive, and efficient secondary analysis is integrated into the NovaSeq X Series with DRAGEN onboard.
DRAGEN onboard allows you to get variant calls directly from your sequencing system. It offers cost savings as well as flexible local and cloud options for every stage of the informatics workflow—sample management, run planning/management, data analysis, and interpretation.
A secure genomic data platform to operationalize informatics and analyze, manage, aggregate, mine, and explore data more efficiently.
A user-friendly, scalable, and secure cloud-computing platform for storage and analysis of genomic data, with a rich ecosystem of BaseSpace Apps.
Laboratory information management system designed for genomics labs to track samples and manage workflows for an optimized and efficient lab.
This platform provides accurate, ultra-rapid secondary genomic analysis of sequencing data.
Streamline your tertiary analysis workflows for rare disease genomics and other germline research applications.
Get up and running quickly with a rental or leasing program designed to work with your budget.