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.
Take advantage of a broad range of techniques, from targeted RNA to single-cell and whole-transcriptome sequencing.
Both genome-wide analysis and targeted approaches can provide insight into methylation patterns at a single nucleotide level.
Cost-effectively run data-rich applications and process more samples to increase statistical power.
Find out more about how library prep works, and explore user-friendly solutions. 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.
NGS is uniquely positioned in an infectious disease surveillance and outbreak model. Explore methods and find solutions to detect and characterize SARS-CoV-2 and other respiratory pathogens, track transmission routes, study co-infection, and investigate viral evolution.Learn More About Coronavirus Sequencing
NGS-based sequencing methods allow cancer researchers to detect rare somatic variants, tumor subclones, and circulating DNA fragments. Explore cancer sequencing methods.
From environmental metagenomics studies to infectious disease surveillance and more, sequencing can help researchers gain genetic insight into bacteria and viruses. Learn more about microbial genomics.
Illumina sequencing is introducing new avenues for understanding autoimmune and rheumatic diseases, atherosclerosis, neurological diseases, and psychiatric 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 health journey. Explore reproductive health solutions.
These videos provide expert tips for common issues such as overclustering, inconsistent quantitation, preventing contamination, and determining if your sequencing insert is too short.
The user-friendly "Recommended Links" feature allows you to easily find content and products relevant to your specific field of interest. You can access this option from the top of any illumina.com page.