MiSeq i100 Series Reagent Kits
Reagents for the MiSeq i100 Series feature easy-to-use cartridges and multiple flow cell configurations for flexible sequencing options.
Solutions to support the entire workflow
Kits, services, and software for every step of the NGS workflow
Our product portfolio supports you across the entire MiSeq i100 Series workflow, from library prep and panels to sequencing, analysis, and services. Illumina Proactive, a complimentary performance and monitoring service, helps you maximize instrument uptime.
The MiSeq i100 Plus System delivers operational simplicity from setup to data analysis, high data accuracy, and exceptional speed. With ten different reagent configurations that provide an output range of 5–100 million single reads and 1.5–30 gigabases, the MiSeq i100 Series supports scalable throughput and deeper sequencing for a wide range of applications.
A fast, flexible workflow for producing normalized and indexed sequencing libraries from a wide range of DNA input types.
Illumina Microbial Amplicon Prep
A streamlined workflow for producing amplicon sequencing libraries from DNA or RNA input with custom, published, or commercially available primer sets.
Illumina RNA Prep with Enrichment
A fast, integrated workflow for producing enriched and indexed sequencing libraries from a broad range of sample types and RNA input quantities.
MiSeq i100 Series reagents combine the power of XLEAP-SBS chemistry with flexible, efficient, and sustainable workflows.
MiSeq i100 Series software and informatics
Simplified data analysis onboard the instrument or in the cloud with DRAGEN secondary analysis, optimized for scientists with minimal bioinformatics expertise.
Track samples, optimize procedures and workflows, and automate routine tasks with a highly customizable laboratory information management system (LIMS).
Efficiently plan and monitor runs while accessing a robust ecosystem of analysis apps in a user-friendly, cloud-based environment.
Perform accurate, ultrarapid secondary genomic analysis of sequencing data.
Operationalize bioinformatics by processing, aggregating, and analyzing data at scale, and configure automated analysis with customizable workflows or ready-to-use DRAGEN pipelines within a secure, scalable data platform.
Streamline germline variant interpretation and research report generation for rare and genetic diseases, hereditary cancer risk and other genetic screening applications, cytogenomics, and large cohort studies.
Streamline variant interpretation and reporting for somatic oncology research applications.
This video walks you step-by-step through planning your run, preparing your samples for sequencing, and setting up the instrument.