Sequencing may be utilized to determine the order of nucleotides in small targeted genomic regions or entire genomes. Illumina sequencing enables a wide variety of applications, allowing researchers to ask virtually any question related to the genome, transcriptome, or epigenome of any organism. Next-generation sequencing (NGS) methods differ primarily by how the DNA or RNA samples are prepared and the data analysis options used.
Find the right sequencer to advance your research.
Analyze the entire genome, focus on regions of interest with whole-exome and targeted sequencing, or study DNA-protein interactions.Learn More
Take advantage of a broad range of techniques, from targeted RNA to single-cell and whole-transcriptome sequencing.Learn More
Both genome-wide analysis and targeted approaches can provide insight into methylation patterns at a single nucleotide level.Learn More
Library preparation options are available for a broad range of sequencing methods, including whole-genome sequencing, whole-exome and targeted sequencing, RNA sequencing, methylation sequencing, and more. These solutions accommodate a variety of throughput needs, from manual protocols to fully automated workstations.
NGS-based sequencing enables cancer researchers to detect rare somatic variants, tumor subclones, and circulating DNA fragments. Learn more about sequencing for cancer research.
From environmental metagenomics studies to infectious disease surveillance and more, NGS-based sequencing can help researchers gain genetic insight into bacteria and viruses. Learn more about microbial genomics.
Illumina sequencing is introducing new avenues for understanding immunological, neurological, and other complex disorders on a molecular level. Learn more about complex disease genomics.
Illumina sequencing and array technologies deliver fast, accurate information that can guide choices along the reproductive and genetic health journey. Find reproductive and genetic health solutions.