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.
Explore the breakthroughs, advancements, and progress
Discover the entire genome with whole-genome solutions, or focus on specific regions of interest with whole-exome and targeted sequencing options.Learn More
Take advantage of a broad range of sequencing techniques for targeted RNA or whole-transcriptome studies.Learn More
Enhance epigenetic studies with high-coverage density and flexibility enabled by sequencing-based DNA methylation analysis.Learn More
Library preparation kits are available for all sequencing methods, including whole-genome sequencing, whole-exome and targeted sequencing, RNA sequencing, methylation sequencing, and more. Kits accommodate a range of throughput needs, from manual protocols to fully automated workstations.Learn More