Products for clinical cancer researchers

Clinical Cancer Research Products

Illumina sequencing and array products facilitate clinical cancer research by providing expert-defined gene content, accurate data, and simple analysis and reporting options.

  • 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 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 Tumor 170—Comprehensive research panel detects single-nucleotide variants (SNVs), amplifications, and fusions that contribute to solid tumor progression.
  • TruSight Oncology UMI Reagents—The TruSight Oncology UMI Reagents and UMI Error Correction App reduce error rates in samples to ≤0.007%, enabling the detection of low frequency variants.
  • 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.
  • TruSight Myeloid Sequencing Panel—Expert-defined research panel targeting oncogenic exons and tumor suppressor genes for myeloid malignancies.
  • TruSight Cancer Sequencing Panel—Expert-defined research panel targeting 94 genes and 284 SNPs associated with cancer predisposition.
  • TruSight Oncology 500—Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
See All Illumina Cancer Research Panels
  • 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.
  • MiSeqDx Instrument—Benchtop sequencer that provides a research mode to generate accurate, reliable data.
  • NextSeq 550 System—Sequencing and cytogenomic array scanning on a single system, with a simple transition between applications.
Exclusive Offer for TruSight Oncology 500

Purchase the TruSight Oncology 500 assay for the first time and receive an exclusive limited time offer.

Learn More
Exclusive Offer for TruSight Oncology 500
  • Local Run Manager—An on-instrument solution for creating a sequencing run, monitoring run status, analyzing sequencing data, and viewing results.
  • BaseSpace Sequence Hub—The Illumina genomics computing environment for NGS data analysis and management.
  • MiSeq Reporter—Easy-to-use software for analysis and variant calling on the MiSeq System.
  • VariantStudio Software—A powerful analysis and reporting tool that provides biological insight into genomic variant data.
  • BlueFuse Multi Software—Widely used, scalable analysis software for cytogenetic studies.
  • 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.
Interested in receiving newsletters, case studies, and information on cancer genomics? Enter your email address.