Illumina Products & Reviews

Simple, comprehensive solution for clinical laboratory environments

Benchtop IVD sequencing to enable labs to run diagnostic assays and develop a range of applications from targeted panels to WGS

Scalable throughput and flexibility for virtually any sequencing method, genome, and scale of project.

Robust performance with tailored content for disease research

An efficient, fast, and integrated library preparation workflow that yields highly accurate data for sensitive sequencing applications.

The NovaSeq 6000Dx is an IVD-compliant high-throughput sequencing instrument for the clinical lab.

A complete targeted resequencing solution for a wide range of applications, with fast integrated workflow and options for custom and fixed enrichment panels.

A suite of bioinformatics pipelines to process NGS data and maximise genomic discovery.

Submicron resolution and high sample throughput deliver exceptional data quality and rapid scan times.

A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.

Illumina 5-base solution for methylation and variant detection

The NovaSeq X and NovaSeq X Plus Sequencing Systems deliver extraordinary throughput and accuracy to perform data-intensive applications at production scale.

Expansive application breadth and operational simplicity with proven performance

The first CE-marked IVD kitted solution for comprehensive genomic profiling (CGP) of DNA and RNA variants, plus MSI and TMB, for multiple solid tumor types.

The new standard in benchtop sequencing speed and simplicity

Comprehensive in-lab NIPT IVD solution including reagents, instruments, and software for accurate aneuploidy screening results in 26 hours.