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. Learn about a wide variety of sequencing methods, and find sequencing instruments, kits, and data analysis solutions to characterize 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.
Learn more about DNA Sequencing »
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.
Learn more about RNA Sequencing »
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.
Learn more about:
Learn about the broad range of experiments you can perform with NGS (next-generation sequencing).
Access our extensive collection of sequencing library preparation methods.
Find methods »