Explore Illumina Mobile Tools
Library Prep and Array Kit Selector
Gene Panel Finder
Sequencing Method Selector
Sequencing Platform Comparison Tool
Find Your Area of Interest
Molecular Biology Research Tools
Applied Genomics Solutions
Genomics in Drug Development
Complex Disease Genomics
Commercial Agricultural Applications
Infectious Disease Surveillance
Biobank Analysis Solutions
Illumina Clinical Services Laboratory
Reproductive & Genetic Health
Explore Research Techniques
Popular Genomics Applications
Sequencing Data Analysis
Explore Our Entire System Portfolio
Find the right system for your application needs.
Browse by Type:
Use Our Interactive Selection Tool:
Browse by System:
Explore Our Products
Browse by Product Type:
Clinical Research Products
Molecular Biology Reagents
Browse All Products
Browse by Area of Interest:
Find Products for Your System:
Additional Product Selection & Experiment Planning Tools:
See All Tools
Access Informatics Solutions
BaseSpace Informatics Suite
Scientific & Educational Content
Sequencing Method Explorer
Education for Researchers
Learn About Illumina
Doing Business with Illumina
See All Support Options
Support for popular kits
View All Sequencing Kits
View All Array Kits
Support for popular systems
Support for Your System
AutoLoader 2.x Support Links
View All AutoLoader 2.x Support
BeadArray Reader Support Links
View All BeadArray Reader Support
BeadXpress Reader Support Links
View All BeadXpress Reader Support
cBot Support Links
View All cBot Support
cBot 2 Support Links
View All cBot 2 Support
Cluster Station Support Links
View All Cluster Station Support
Popular Kits for Cluster Station
Genome Analyzer IIx Support Links
View All Genome Analyzer IIx Support
Popular Kits for Genome Analyzer IIx
View All Supported Kits
HiScan Support Links
View All HiScan Support
Popular Kits for HiScan
HiSeq 1000 Support Links
View All HiSeq 1000 Support
Popular Kits for HiSeq 1000
HiSeq 1500 Support Links
View All HiSeq 1500 Support
Popular Kits for HiSeq 1500
HiSeq 2000 Support Links
View All HiSeq 2000 Support
Popular Kits for HiSeq 2000
HiSeq 2500 Support Links
View All HiSeq 2500 Support
Popular Kits for HiSeq 2500
HiSeq 3000 Support Links
View All HiSeq 3000 Support
Popular Kits for HiSeq 3000
HiSeq 4000 Support Links
View All HiSeq 4000 Support
Popular Kits for HiSeq 4000
HiScanSQ Support Links
View All HiScanSQ Support
Popular Kits for HiScanSQ
HiSeq X Support Links
View All HiSeq X Support
Popular Kits for HiSeq X
iScan Support Links
View All iScan Support
Popular Kits for iScan
MiniSeq Support Links
View All MiniSeq Support
MiSeq Support Links
View All MiSeq Support
Popular Kits for MiSeq
MiSeqDx Support Links
View All MiSeqDx Support
Popular Kits for MiSeqDx
MiSeq FGx Support Links
View All MiSeq FGx Support
Popular Kits for MiSeq FGx
NextSeq 500 Support Links
View All NextSeq 500 Support
Popular Kits for NextSeq 500
NextSeq 550 Support Links
View All NextSeq 550 Support
Popular Kits for NextSeq 550
NeoPrep Library Prep System Support Links
View All NeoPrep Library Prep System Support
Popular Kits for NeoPrep Library Prep System
NovaSeq 6000 Support Links
View All NovaSeq 6000 Support
Support for Popular Kits
Support for your organization
Support for your workflow
Helpful tools and tips
Support for Your Workflow
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.
Prepare sequencing libraries for small genomes, PCR amplicons, plasmids, or cDNA in less than 90 minutes, with a low DNA input requirement.
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.
Simple, all-inclusive whole-genome sequencing (WGS) library preparation that provides accurate and comprehensive coverage of complex genomes.
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.
The TruSeq RNA Library Preparation Kits provide a simple, cost-effective solution for analysis of the coding transcriptome.
These kits provide a simple, cost-effective solution for generating miRNA and small RNA sequencing libraries directly from total RNA, for any species.
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.
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.
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.
PhiX Control v3 is a ready-to-use control library for Illumina sequencing runs.
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.
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.
This kit removes unwanted ribosomal RNA and globin mRNA from mammalian blood RNA samples before sequencing.
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.