Sequence the entire genome of a bacterium, virus, or other microbe.
Next-generation sequencing offers the sensitivity and specificity that researchers need to detect low levels of circulating tumor DNA in the bloodstream.
Sequence thousands of organisms in parallel. Identify unculturable or low-abundance microbes, or evaluate microbial diversity.
Capture genomic regions of interest via hybridization to target-specific biotinylated probes.
Analyze coding plus multiple forms of noncoding RNA for a comprehensive picture of the transcriptome.
Select and sequence specific transcripts of interest for gene expression profiling studies.
Enhance epigenetic studies with high-coverage density and flexibility enabled by sequencing-based DNA methylation analysis.
Chromatin immunoprecipitation sequencing (ChIP-Seq) is a powerful method for analyzing DNA-protein interactions and performing genome-wide surveys of gene regulation.
The assay for transposase-accessible chromatin with sequencing is a popular method for determining chromatin accessibility across the genome.
Ultra-deep sequencing of PCR amplicons enables cost-effective analysis of up to hundreds of target genomic regions in one assay.
Learn how to use the PhiX library as a control in your Illumina sequencing runs.
*The NextSeq 1000 and NextSeq 2000 Systems are scalable platforms that can support a broad range of current and emerging applications beyond those listed here.
The NextSeq 1000 and NextSeq 2000 Systems offer an intuitive workflow with load-and-go ease, on-board informatics, and flexibility to run many NGS applications. Register to see a virtual instrument demo and learn more about these solutions enabled by our newest platform, followed by open audience Q&A.View Webinar
These summaries of peer-reviewed publications highlight how Illumina technology is furthering research.
Ask virtually any question related to the genome, transcriptome, or epigenome of any organism. Explore a broad range of NGS methods.
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