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Access a wider range of informative SNPs with a single kit. Includes all reagents to prepare sequencing libraries from forensic DNA samples.
Nextera DNA kits provide a fast and easy library prep workflow, delivering whole-genome sequencing libraries in under 90 min.
This library preparation kit offers a gel-free method for preparing up to 12 kb mate pair libraries with the industry’s lowest DNA input requirement.
Custom target enrichment kit to rapidly interrogate those portions of the human genome most important to your specific research.
Identify coding variants up to 70% faster with this exome library prep and enrichment kit. Expanded kit sequences untranslated regions (UTRs) and miRNA.
Prepare sequencing libraries for small genomes, PCR amplicons, plasmids, or cDNA in less than 90 minutes, with a low DNA input requirement.
A robust, scalable, and user-friendly workflow for transcriptome profiling of hundreds to tens of thousands of single cells in a given experiment.
This high-value solution for parentage testing of multiple beef and dairy cattle breeds includes genotyping of relevant traits in a single assay.
Simple, cost-effective chromatin immunoprecipitation sequencing (ChIP-Seq) DNA library preparation, with master mixes and robust multiplex capabilities.
This library prep kit delivers sensitive and specific amplicon sequencing results from both low-input and FFPE DNA samples.
Focus on key genomic regions of interest with this targeted resequencing solution, useful for very high plexity pools or longer amplicons.
Converts bisulfite-treated, single-stranded DNA into an Illumina sequencing library. Enables comprehensive whole-genome DNA methylation analysis.
Simple, all-inclusive whole-genome sequencing (WGS) library preparation that provides accurate and comprehensive coverage of complex genomes.
This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths.
This kit combines next-generation sequencing with epigenetic insights to accelerate biomarker discovery and understand methylation’s role in gene regulation.
Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA.
DNA library preparation for use with the NeoPrep System, providing comprehensive genomic coverage with low DNA input and minimal hands-on time.
Provides a reproducible, economical solution for sequencing RNA from FFPE tissues and other low-quality samples. Accuracy from as little as 10 ng total RNA.
The TruSeq RNA Library Preparation Kits provide a simple, cost-effective solution for analysis of the coding transcriptome.
This exome sequencing library prep kit uses a simple, one-day workflow to provide a fast path to greater understanding of the human exome.
The TruSeq Ribo Profile kit (formerly ARTseq) sequences ribosome-protected mRNA fragments to provide a snapshot of the active ribosomes in a cell.
These kits provide a simple, cost-effective solution for generating miRNA and small RNA sequencing libraries directly from total RNA, for any species.
A robust, highly scalable whole-transcriptome analysis (RNA-Seq) solution for a variety of species and sample types, including human, mouse, and FFPE.
Prepare whole-transcriptome sequencing libraries from blood-derived RNA with an efficient workflow that removes rRNA and globin mRNA in a single step.
Capture a comprehensive view of the plant transcriptome with this RNA-Seq library prep kit. Remove rRNA from plant leaf, seed, and root tissue.
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information.
Complete view of the transcriptome with walk-away workflow, lower input requirement, and excellent reproducibility.
Use this sequencing kit to prepare DNA libraries to generate synthetically long reads, with informatics options for genome assembly or genome phasing.
A targeted RNA sequencing panel for studying apoptosis, or programmed cell death. Assay targets pro-apoptotic and anti-apoptotic genes.
A targeted RNA sequencing panel to study cellular pathways affected by cardiotoxic compounds or stress. Assay targets cardiotoxic response markers.
A targeted RNA sequencing panel for studying the cell cycle. Assays target genes involved in all cell cycle phases as well as DNA replication.
A targeted RNA sequencing panel for studying cytochrome p450 (CYP) genes. Assays target CYP genes involved in drug and toxin metabolism.
A targeted RNA sequencing panel for studying hedgehog signaling. Assays target upstream and downstream signal transduction and transcription factors.
Targeted RNA assays for gene expression studies: fixed or custom sequencing panels, with a simple workflow and automated data analysis.
A targeted RNA sequencing panel for studying NFκB signaling. Assays target upstream and downstream signal transduction and NFκB transcription factors.
A targeted RNA sequencing panel for studying neurodegenerative and neurotoxic pathways such as those implicated in Alzheimer’s Disease.
A targeted RNA sequencing panel for studying various stem cell types. Analyze stem cell and pluripotency markers, cytokines, growth factors, and more.
A targeted RNA sequencing panel for studying Wnt signaling. Assays upstream and downstream signal transduction genes, transcription factors, and more.
A targeted RNA sequencing panel for studying p53 signaling. Assays target genes involved in signal transduction, as well as transcription factors.
This kit enables cluster generation for subsequent sequencing on the HiSeq 3000 and HiSeq 4000 Systems.
Includes sequencing reagents specifically designed for the HiSeq 3000/HiSeq 4000 Systems. Enables production-scale sequencing for diverse applications.
Provides reagents for Single Read (SR) cluster generation on the cBot2 System. Cluster reagents are compatible with the HiSeq 3000 and HiSeq 4000 Systems.
This kit uses isothermal amplification to create clonal clusters of ~1000 copies each, ready for sequencing on enabled HiSeq systems.
HiSeq Rapid Cluster Kits v2 enable an on-board cluster generation process, designed to be used in HiSeq Rapid Run mode.
The HiSeq Rapid Duo cBot Sample Loading Kit doubles the indexing capability achieved with the on-board cluster generation process alone.
HiSeq Rapid SBS Kits v2 are designed for the rapid run mode of HiSeq 2500 and 1500 sequencers.
Reagents for determining the DNA sequence of each cluster on a flow cell using sequencing by synthesis technology on enabled HiSeq systems.
The HiSeq SR (Single Read) Cluster Kit v4 cBot uses isothermal amplification to create clonal clusters of ~1000 copies each, ready for sequencing on enabled HiSeq systems.
Kits include SBS reagents, clustering reagents, and patterned flow cells for increased cluster density and simplified image analysis, compared to non-patterned flow cells.
The MiSeq FGx Reagent Kit is specifically designed for use with the MiSeq FGx Forensic Genomics System.
Optimized chemistry to increase cluster density and read length, and improve sequencing quality scores, compared to earlier MiSeq reagent kit versions.
MiSeq sequencing reagents in pre-filled, ready-to-use cartridges. Micro and nano formats are available for low output applications.
MiniSeq Reagent Kits bring the power of Illumina NGS to labs of all sizes. Access cost-efficient sequencing, even for low numbers of samples.
These sequencing reagent kits offer a simplified workflow and improved data quality compared to the prior v1 kit version.
Reagent kits for the NovaSeq 5000 and NovaSeq 6000 Systems provide ready-to-use cartridge-based reagents for cluster generation and SBS.
PhiX Control v3 is a ready-to-use control library for Illumina sequencing runs.
These primers are required to sequence Nextera, TruSeq Synthetic Long-Read DNA, or TruSeq HT libraries in certain cases, as indicated.
This kit, when used with the cBot, enables cluster generation for subsequent paired-end sequencing on the Genome Analyzer IIx.
This kit enables cluster generation for subsequent paired-end sequencing on select HiSeq Systems as well as the HiScanSQ System.
This kit, when used with the Cluster Station, enables cluster generation for subsequent paired-end sequencing on the Genome Analyzer IIx.
TruSeq Rapid Cluster Kits - PE (paired-end) and SR (single-read) - are designed for use in the rapid run mode of HiSeq 2500 and 1500 sequencers.
This duo kit enables individually addressable lanes. It requires a cBot and is designed for the rapid run workflow of HiSeq 2500 and 1500 sequencers.
Designed for the rapid run mode of HiSeq 2500 and 1500 sequencers, these kits enable high data quality, fast turnaround time, and a walk-away workflow.
These kits contain ready-to-load reagents to determine the DNA sequence of each cluster on a HiSeq flow cell using sequencing by synthesis technology.
This sequencing kit for the Genome Analyzer IIx System permits users to extend read lengths to 2 x 150 and achieve up to 95 Gb of mappable data.
This kit provides reagents for cluster amplification on single-read flow cells. It is designed for use with the Genome Analyzer IIx with cBot.
Use this kit to cluster a flow cell on the cBot for subsequent single-read sequencing in the TruSeq v3 high output mode on enabled HiSeq systems.
This kit, when used with the Cluster Station, enables cluster generation for subsequent single-read sequencing on the Genome Analyzer IIx.
This comprehensive genome-wide bovine genotyping array kit features over 777,000 SNPs, and is compatible with any breed of beef or dairy cattle.
Extend genomic selection to the entire herd with scalable content at an economical price.
This BeadChip microarray provides high density multi-sample bovine genotyping for genome characterization of major dairy and beef cattle breed types.
This array enables genotyping of any domestic dog breed, and offers ample SNP density for within-breed association and CNV studies.
These 24-sample arrays enable economical large-scale human genotyping studies, with high-throughput processing capabilities, and the option to add up to 300K semi-custom markers.
This DNA microarray kit delivers genome-wide SNP and genetic variant information for genetic studies, especially large-scale human genotyping studies.
Infinium Exome-24 Kit arrays deliver exceptional coverage of putative functional exonic variants representing diverse populations and a range of common conditions.
GSA is a next-generation genotyping array for population-scale genetics, variant screening, and precision medicine research.
The Infinium ImmunoArray-24 v2 BeadChip is the next-generation genotyping array for detecting genetic variation in the immune system.
Robust methylation profiling microarray with unparalleled coverage of CpG islands, genes, and enhancers. Use for epigenome-wide association studies.
A cost-effective array for understanding complex disease in diverse human populations, focused on Hispanic and African American populations.
A cost-effective array for understanding complex disease in diverse human populations, focused on European, East Asian, and South Asian populations.
A cost-effective array for understanding complex disease in diverse human populations.
This 8-sample BeadChip array features ~2.5 million markers, with custom marker add-on capability, and delivers exceptional genomic coverage rates across diverse populations.
Comprehensive coverage and functional exonic content for next-generation genotyping, GWAS, and CNV analysis.
This 4-sample BeadChip array, optimized for whole-genome genotyping and CNV studies, covers > 4.3 million variants.
This BeadChip array covers > 4.3 million whole-genome variants down to 1% minor allele frequency (MAF), plus novel functional exonic variants.
This 24-sample BeadChip array offers exceptional throughput of thousands of samples per week, enabling powerful human genome-wide association studies (GWAS).
Discover novel trait and disease associations with optimized tag SNPs and functional exonic content at an attractive price.
Advance your Chinese population GWAS. This microarray provides coverage of common, intermediate, and rare variation specific to Chinese populations.
This comprehensive, high-density microarray kit enables research into cancer predisposition and risk.
A cost-effective, high-density Illumina microarray for large-scale genetic studies focused on psychiatric predisposition and risk.
genotyping for quality control, tracking, and stratification applications including biobanking.
This BeadChip microarray offers a high-powered genotyping solution to advance aquaculture breeding programs of Pacific white shrimp.
Infinium XT is a comprehensive microarray solution that enables production-scale genotyping of up to 50,000 single or multi-species custom variants.
Interrogate virtually any target across any species to create a fully-customized genotyping array tailored to your unique study needs.
Content for essentially derived varieties assessment and maize breeding applications. Samples used include the Plant Variety Protection Act panel.
This array enables genetic variation analysis across maize lines. It includes over 50,000 validated markers derived from the B73 corn reference sequence.
This array features over 54,241 evenly spaced SNP probes for genome-wide association studies, genome-wide selection, and genetic merit determination.
This 24-sample genome-wide genotyping array detects over 64,000 evenly distributed SNPs for genetic variation analysis of multiple porcine breeds.
BaseSpace Clarity LIMS is a laboratory information management system that helps laboratories track samples and optimize procedures and workflows.
BaseSpace Cohort Analyzer allows you to integrate and analyze subject and genomic data together using innovative visualization and analysis tools.
BaseSpace Correlation Engine mines over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research.
Simplify your bioinformatics with an economical and powerful computing environment to manage, analyze, and share data.
BaseSpace Variant Interpreter (Beta) enables genetic testing labs to rapidly annotate, filter, and interpret genomic data.
Widely used microarray and proven method for accurate, timely preimplantation genetic screening results.
Microarray to assay whole chromosome copy number imbalances and subchromosomal structural imbalances in polar bodies, blastomeres and blastocysts.
This BeadChip array is optimized for cytogenetic studies using formalin-fixed paraffin-embedded (FFPE) paired tumor-normal samples.
This 12-sample BeadChip array enables analysis of genetic and structural variation in the human genome, such as duplications, deletions, amplifications, copy-neutral LOH, and mosaicism.
This genome-wide karyomapping microarray provides insight into the inheritance of single-gene defects by testing single cells from embryo biopsies.
This consortium-built array provides comprehensive coverage of cytogenetically relevant genes for congenital disorders and cancer research.
Whole-genome amplification of total DNA from a single embryonic cell, or a few embryonic cells, for use in the karyomapping assay protocol.
Used to generate a DNA template from single cells. Ideal for use with 24sure aneuploidy screening arrays or VeriSeq PGS applications.
Amplified genomic DNA recommended for use as part of the 24sure protocols when analyzing amplified DNA from a single cell or a few cells.
The TruSeq Amplicon - Cancer Panel is a highly multiplexed targeted resequencing assay for detecting somatic mutations.
This expert-defined sequencing panel targets 94 genes and 284 SNPs associated with a predisposition towards various cancers.
This kit provides researchers with a comprehensive, cost-effective solution for identifying causal variants implicated in inherited cardiac conditions (ICCs).
Unambiguous, phase-resolved HLA typing in a single assay using proven Illumina NGS technology and Assign analysis software.
TruSight Inherited Disease is a targeted sequencing panel that focuses on 552 genes associated with severe, recessive pediatric onset diseases.
The TruSight Myeloid Sequencing Panel targets variants associated with myeloid malignancies such as AML, MDS, MPN, CML, CMML, and JMML.
This panel focuses on exonic regions harboring disease-causing variants. Labs can perform commonly ordered molecular assays on-site with one assay.
Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples.
Targeting 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types including blood, bone marrow, and FFPE.
TruSight Rapid Capture all-in-one kits enable targeted sequencing library preparation and enrichment for up to 96 samples in only 1.5 days.
Focused sequencing panel to assess 15 genes that are commonly mutated in solid tumors in a single assay, with a simple, rapid workflow.
Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.
This targeted sequencing panel enables clinical researchers to identify low-frequency variation in solid tumors across 26 genes.
A fully validated next-generation sequencing solution for PGS, providing accurate results in aneuploidy screening and extending future opportunities.
FDA-cleared NGS assay with the largest panel of clinically relevant, functionally validated cystic fibrosis variants in a diverse population.
FDA-cleared next-generation sequencing assay provides a full view of coding regions of the CFTR gene, to aid in in vitro diagnosis of cystic fibrosis.
A validated, FDA-cleared kit that enables molecular diagnostic laboratories to design their own next-generation sequencing assays for use on the MiSeqDx System.
Reagents, instruments, and CE-IVD marked library prep and analysis/reporting software in an automated workflow for in-lab prenatal aneuploidy screening.
This kit removes unwanted ribosomal RNA and globin mRNA from mammalian blood RNA samples before sequencing.
Evaluate sample quality and repair degraded FFPE DNA samples for use in Infinium array-based assays.
This kit removes cytoplasmic and mitochondrial rRNA from samples composed of human/mouse/rat, Gram-positive and Gram-negative bacterial RNA.
This kit removes both cytoplasmic and mitochondrial rRNA from human, mouse, and rat samples, including partially degraded samples.
This kit removes both cytoplasmic and mitochondrial ribosomal RNA from yeast samples.
This kit removes ribosomal RNA from Gram-positive and Gram-negative bacterial mixtures in a single pass.
This kit removes unwanted ribosomal RNA from Gram-negative bacterial samples.
This kit removes unwanted ribosomal RNA from Gram-positive bacterial samples.
This kit removes cytoplasmic ribosomal RNA from human, mouse, or rat samples, including partially degraded samples.
This kit removes cytoplasmic, mitochondrial, and chloroplast ribosomal RNA from plant seed, root, or leaf samples in a single pass.
This device automatically loads BeadChip microarray carriers onto scanning systems.
Boxes each store up to 25 BeadChips.
Used to handle BeadChips following microarray hybridization.
The Illumina Hybridization Oven is a high-capacity hybridization (hyb) oven
that is customized for Illumina assays.
Use to ensure correct assembly and optimal processing for the Infinium Assay.
The Infinium BeadChip Expansion Package enables processing of eight additional BeadChip arrays per day.
These kits include the hardware, software, and accessories needed to process multiple BeadChip array samples in parallel.
These chambers are used for BeadChip array hybridization during Infinium Assays.
Wash dish and staining rack used in BeadChip processing.
Thermometer and temperature probe to read the temperature in the TeFlow rack during Infinium assays.
Fits in the HybEx Heating System used with Infinium Assays.
These replacement probes are compatible with the liquid-handling robots used to automate Illumina array-based assays.
The Tip Depth Gauge calibrates the probe depth for liquid-handling robots used to automate Illumina array-based assays.
These tubes enable sequencing sample tracking on the cBot 2 automated cluster generation system.
The cBot 2 System streamlines the sequencing workflow by automating cluster generation. It is a required accessory instrument for HiSeq sequencers.
These packages include robotic liquid handling capabilities, control software, and other automation options to streamline the array workflow and reduce errors.
Explore the entire portfolio of Illumina sequencing and microarray systems.
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