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.

Oncology
  • 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.
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.
  • 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.
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