Clinical Cancer Research Products
Products to Facilitate Clinical Cancer Research
Illumina sequencing and array products facilitate clinical cancer research by providing expert-defined gene content, accurate data, and simple analysis and reporting options.
Featured Sequencing Research Panels
- AmpliSeq for Illumina Sequencing Panels—Optimized for clinical cancer research applications and available as predesigned or made-to-order panels; use with targets ranging from a few to hundreds of genes in a single run.
- TruSight Tumor 170—Comprehensive research panel detects single-nucleotide variants (SNVs), amplifications, and fusions that contribute to solid tumor progression.
- TruSight Oncology 500—Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
- TruSight RNA Fusion—This targeted RNA sequencing research panel is a cost-effective solution to detect gene fusions in multiple cancer types, regardless of origin.
- TruSight RNA Pan-Cancer—Targeting 1385 oncology genes for gene expression, variant and fusion detection studies in all RNA sample types including FFPE.
- TruSight Tumor 15—Focused research panel to assess relevant solid tumor somatic variants in a simple, sample-to-data workflow.
Sequencing Systems
- iSeq 100 System—Affordable, fast, and accessible sequencing power for targeted or small genome sequencing in any lab.
- MiniSeq System—Supports a broad range of targeted DNA and RNA applications.
- MiSeq System—Benchtop sequencer featuring a simple workflow and integrated data analysis software.
- NextSeq 550 System—Sequencing and cytogenomic array scanning on a single system, with a simple transition between applications.
- NextSeq 1000 & 2000 Systems—75 breakthrough innovations and our simplest workflow yet.
- NovaSeq 6000 System—Scalable throughput and flexibility for virtually any sequencing method, genome, and scale of project.
Exclusive Offer for TruSight Oncology 500
Purchase the TruSight Oncology 500 assay for the first time and receive an exclusive limited time offer.
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Sequencing Data Analysis and Storage
- BaseSpace Sequence Hub—The Illumina genomics computing environment for NGS data analysis and management.
- DRAGEN Bio-IT Platform—Provides accurate, ultra-rapid secondary genomic analysis of sequencing data.
- Local Run Manager—An on-instrument solution for creating a sequencing run, monitoring run status, analyzing sequencing data, and viewing results.
- MiSeq Reporter—Easy-to-use software for analysis and variant calling on the MiSeq System.
- BlueFuse Multi Software—Widely used, scalable analysis software for cytogenetic studies.
Microarrays
- Infinium OncoArray-500K BeadChip—An expert-designed, high-density array for researching cancer predisposition and risk. Contains ~500,000 genome-wide SNPs, plus putative SNPs associated with breast, colorectal, lung, ovarian, and prostate cancer.
- Infinium iSelect Custom Genotyping BeadChips—Design-your-own custom genotyping panels for interrogation of up to 1 million markers (SNPs, indels, CNVs).
- Infinium CytoSNP-850K BeadChip—Designed by international consortia to provide the most comprehensive coverage of cytogenetically relevant genes for cancer studies.