Sequencing is the process of determining the order of nucleotide bases (A,C,T, and G) within a stretch of DNA. Sequencing the entire complement of DNA, or genome, of many animal, plant, and microbial species is indispensable for basic biological and medical research. Illumina offers a variety of sequencing instruments, kits, and data analysis solutions that enable characterization of the genome, epigenome, and transcriptome.
Access the broadest range of genomic sequencing applications for DNA analysis. Characterize genes, regions, or entire genomes with proven solutions for whole-genome or targeted sequencing, including exomes, amplicons, and de novo studies.
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Revolutionize gene expression profiling and transcriptome analysis with RNA sequencing. Align reads across splice junctions to identify isoforms and fusions. Quantify both rare and common transcripts. Derive precise strand information, and sequence low-quality or FFPE samples.
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Use sequencing to analyze epigenetic modifications and obtain the most complete view of gene regulation mechanics. Examine CpG methylation, histone modifications, chromatin structure, DNA-protein interactions or transcriptome profiling with a broad portfolio of sequencing tools.
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An extensive collection of library preparation methods.View the poster » (PDF 23 MB)
Sequencing Sample Prep Kit Selector »
Zero in on the best kit for your application.