NextSeq 500 Applications

Sequencing for Any Application

With the highest output of any desktop sequencer, the NextSeq 500 Sequencing System enables researchers to perform the widest range of sequencing applications. The flexible, scalable system offers tunable read lengths and output options to support research needs.

High-Output Kit
 
 
Mid-Output Kit
Up to
400 M
reads
1
whole human genome
9
exomes
10
transcriptomes

Perform the most popular high-throughput applications in less than a day. Easily shift from low to higher throughput processing with each sequencing run.

 
 
Up to
130 M
reads
3
exomes
6
enrichment
panels
96
amplicon
panels

Two flow cell configurations enable you to tune your output as needed. NextSeq 500 is an efficient system to handle a range of project sizes.

 
 

The widest range of applications

Whole-Genome Sequencing
The NextSeq 500 System leverages industry-leading Illumina sequencing technology, delivering the highest coverage to identify variants throughout the genome. With push-button sequencing and minimal hands-on time, the NextSeq whole-genome sequencing solution enables researchers to analyze any genome efficiently, from microbes to humans.

Learn more about whole-genome sequencing »

Exome Sequencing
The NextSeq 500 System offers the simplest and most reliable exome sequencing method to identify true coding variants, successfully sequencing even the most difficult genomic regions. Illumina's exome sequencing solution includes integrated library preparation and exome enrichment, push-button sequencing, and simple data analysis. With minimal hands-on time, researchers can now interrogate more of the exome accurately and efficiently.

Learn more about exome sequencing »

Transcriptome Sequencing
RNA sequencing enables researchers to take a closer look at gene expression and can be used to identify isoforms, novel transcripts, and gene fusions. The NextSeq RNA sequencing solution leverages industry-leading Illumina technology to deliver a detailed snapshot of the complete transcriptome. This solution enables researchers to tailor their studies from gene expression to complex whole-transcriptome profiling.

Learn about transcriptome analysis with RNA sequencing »

Targeted Resequencing
Targeted resequencing involves isolation of genomic regions of interest in a sample library, enabling cost-effective and systematic detection of germline and somatic variants. Illumina offers a range of targeted sequencing solutions to support a variety of next-generation sequencing (NGS) study designs, from targeted gene panels, such as TruSight One Sequencing Panel.

Learn more about targeted resequencing »

For Research Use Only.

Access the Whole Genome

See how Illumina technology provides high-quality data to ensure accurate variant identification across an entire genome.

Access PDF »

Identify True Coding Variants

Learn how you can use the NextSeq 500 System to evaluate the exome accurately and cost-effectively.

Access PDF »

Gain a Complete View of the Transcriptome

See how the NextSeq 500 System provides a scalable approach for RNA sequencing, with higher sensitivity and accuracy than conventional arrays.

Access PDF »