MiniSeq System sequencing reagent kits bring the power and reliability of proven Illumina next-generation sequencing (NGS) to labs of all sizes. Access cost-efficient sequencing with high data quality, even for low numbers of samples.Learn More
Targeted research panel investigating somatic and germline variants in BRCA1 and BRCA2.
Targeted DNA and RNA research panel investigating 52 genes with known relevance to solid tumors.
Targeting 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types including blood, bone marrow, and formalin-fixed, paraffin-embedded (FFPE) tissue.
These expert-defined sequencing research panels target 94 genes and 284 SNPs associated with a predisposition towards various cancers.
These kits provide a simple, cost-effective solution for generating miRNA and small RNA sequencing libraries directly from total RNA, for any species.
Targeted custom research panels optimized for sequencing specific targets or genomic content of interest.
Local Run Manager is an integrated on-instrument solution for creating a run, monitoring status, analyzing sequencing data, and viewing results. Designed to minimize setup and the risk of user error, the system enables onboard review of real-time data and performance metrics. Researchers can interface with the MiniSeq System from any web browser.Learn More
DesignStudio is a web-based assay design tool to help researchers design and order custom sequencing probes, or create custom genotyping array assays.
Setting up and running sequencing experiments is easy with software tools designed for Illumina sequencing systems.
Simplify your bioinformatics with an economical and powerful computing environment to manage, analyze, and share data.
BaseSpace Correlation Engine mines over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research.
BaseSpace Cohort Analyzer allows you to integrate and analyze subject and genomic data together using innovative visualization and analysis tools.
BaseSpace Variant Interpreter enables genetic labs to rapidly identify biologically significant variants from human genomic data.
Illumina services and support begins when the MiniSeq System is delivered. Illumina scientists and engineers assist with NGS system installation and setup and train laboratory personnel. In addition to onsite support, training courses are available to bring laboratory personnel quickly up to speed.
Illumina scientists are available 24/7 globally to answer questions every step of the way, enabling researchers to focus on making the next breakthrough discovery.
In addition to the 1-year basic service warranty included with system purchase, Illumina offers maintenance, repair, and qualification solutions.
Get high-quality results on Illumina technology even faster with instructor-led or hands-on courses and web-based training options.
Bring an experienced Illumina team to your lab to jump-start successful sequencing workflow implementation.
Verify instrument installation and operation and obtain an audit-ready report to help meet regulatory requirements.
Verify instrument performance and obtain an audit-ready report to help meet regulatory requirements.
Verify instrument operation and obtain an audit-ready report to help meet regulatory requirements.