Targeting known variants for cancer related genes

Fixed and custom panels for cost-effective sequencing and easier data analysis

Illumina offers a broad portfolio of cancer panels and cancer-focused products across multiple application areas. These products have been optimized with clinical cancer research in mind.

Achieve sequence-ready libraries from as little as 1 ng of high-quality input or 10 ng formalin-fixed paraffin-embedded (FFPE) sample using efficient, optimized assays and integrated sequencing and bioinformatics. Our comprehensive offering includes both fixed panels and custom options.

Cancer Panels for Targeted Sequencing

AmpliSeq for Illumina and our TruSight cancer panels offer several library preparation, sequencing, and data analysis options for cancer research. Streamlined library prep workflows and flexible kit configurations accommodate multiple study designs. Illumina systems deliver industry-leading sequencing—in fact, more than 90% of the world’s sequencing data are generated using Illumina sequencing by synthesis (SBS) chemistry.*

Select your application area below to find out more about our product offerings for cancer research.

Multisite Validation of Solid Tumor Panel

Multi-Site Analytical Validation of TruSight Tumor 15 (TST15) Determining Robustness and Concordance

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New Views of Cancer Pathways in Pediatric Leukemia

Researchers are using the TruSight RNA Pan-Cancer Panel to understand the role of fusion genes in pediatric leukemia.

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NGS to Detect Blood Cancers

Targeted NGS can identify myeloid-related genes with greater sensitivity than Sanger sequencing or cytogenetic methods.

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Removing Cancer's Veil: TruSight Tumor 170

A new enrichment-based cancer research assay interrogates both DNA and RNA, detecting small variants, gene amplifications, gene fusions, and splice variants.

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Resources for Onboarding NGS
Resources for Onboarding NGS

View educational resources from recognized oncology experts and regulatory bodies about onboarding NGS.

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Amplicon Sequencing
Amplicon Sequencing

Ultra-deep sequencing of PCR amplicons enables analysis of specific genomic regions of interest.

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References

*Data calculations on file. Illumina, Inc. 2017.