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
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
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.
Products for translational and clinical research, from TruSight sequencing panels to cytogenomic analysis arrays and more.
Find next-generation sequencing (NGS) library preparation solutions for a broad range of DNA, RNA, and epigenetic sequencing methods.
Use this table to decide between various ScriptSeq RNA-Seq library prep kits, compatible with a variety of sample types and species.