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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 for characterizing the genome, epigenome, and transcriptome.
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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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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Find out about the broad range of experiments you can perform with NGS (next-generation sequencing), and learn more about the technology.
Access our extensive collection of sequencing library prep methods.
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See how HiSeq X Ten breaks the $1000 genome barrier for human whole-genome sequencing.