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.
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
Use the beta version of this interactive tool to explore experimental next-generation sequencing (NGS) library preparation methods compiled from the scientific literature. New methods will be continuously added.Find a Method
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