Sequencing only the coding regions of the genome enables researchers to focus on the genes most likely to affect phenotype, and offers an accessible combination of turnaround time and price.
Flexibility to do more
Fuel a broad range of applications, from targeted panels to whole-genome sequencing and more
Sequencing only the coding regions of the genome enables researchers to focus on the genes most likely to affect phenotype, and offers an accessible combination of turnaround time and price.
Illumina DNA Prep with Enrichment + Illumina Exome Panel
A fast, integrated whole-exome enrichment and sequencing library preparation workflow for a wide range of applications.
NextSeq 1000/2000 XLEAP-SBS reagent kits
NextSeq 1000/2000 XLEAP-SBS reagent kits contain a reagent cartridge, flow cell, and resuspension buffer. Multiple flow cell configurations offer adjustable output based on project needs.
Push-button alignment, followed by variant calling of Illumina exomes to rapidly identify disease-associated variants.
The P3 and P4 flow cells on the NextSeq 2000 System are an excellent fit for multiomics studies. Use multiomics to better connect genotype to phenotype and obtain a full cellular readout not found through single-application approaches.
Detect transcriptional activity to resolve mRNA expression at the cellular level in structurally preserved tissues.
Analyze coding plus multiple forms of noncoding RNA for a comprehensive picture of the transcriptome.
Identify unique receptor variants to map the vast repertoire of immune cells capable of recognizing a seemingly boundless array of targets.
Sequence the entire genome of a bacterium, virus, or other microbe for applications in public health, infectious disease surveillance, molecular epidemiology studies, and environmental metagenomics.
Use sequence-specific hybridization to analyze genomic regions of interest.
Select and sequence specific transcripts of interest for gene expression profiling studies.
Hear how the NextSeq 2000 provides scientists with the precision, affordability, and accessibility to make their research a reality.
Learn how the NextSeq 2000 system delivers the flexibility to support your research needs including bulk RNA-Seq, target enrichment, single-cell RNA-Seq, and much more.