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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
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Discover the entire genome with whole-genome solutions, or focus on specific regions of interest with whole-exome and targeted sequencing options.
Learn MoreTake advantage of a broad range of sequencing techniques for targeted RNA or whole-transcriptome studies.
Learn MoreEnhance epigenetic studies with high-coverage density and flexibility enabled by sequencing-based DNA methylation analysis.
Learn MoreUse this interactive tool to explore experimental NGS library preparation methods compiled from the scientific literature.
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 MoreAll the information you need, from library preparation to sequencer selection to analysis. Select the best tools for your lab.
Compare sequencing systems and identify the best option for your lab and applications.
With its unprecedented throughput, scalability, and speed, NGS enables biological studies at a level never before possible.
NextSeq 500 v2 Kits offer better data quality, an improved signal to noise ratio, and a simpler workflow.
These short videos provide expert tips for common issues including overclustering, inconsistent quantitation, and sequencing through the insert.