Targeted cancer sequencing focuses on a select set of genes, gene regions, or amplicons that have known associations with cancer. You can use fixed panels that contain cancer-associated genes or design custom panels based on genes of interest.
Focused panels for targeted cancer sequencing significantly narrow the scope of a sequencing project, reducing cost and data analysis burdens. Because it assesses a limited set of genes, targeted cancer sequencing allows for deeper coverage of those genes and higher sensitivity to call variants in rare tumor subclones confidently.Learn More
Fixed panels offer the reassurance of expertly designed and analytically validated genomic content, focusing on genes with established cancer associations. This enables the highest sensitivity for rare variant calling in all sample types, including formalin-fixed, paraffin-embedded (FFPE) tissue.Access PDF
With custom panels for targeted cancer sequencing, researchers can sequence hundreds of genomic regions of interest in a single panel. Gene content can be completely customized based on study objectives. Custom assays are compatible with various sample types, including FFPE tumors.Learn More
Illumina offers several library preparation, sequencing, and data analysis options for cancer whole-genome sequencing. Streamlined library prep workflows and flexible kit configurations accommodate multiple study designs. Illumina systems deliver industry-leading data quality—in fact, approximately 90% of the world’s sequencing data are generated using Illumina sequencing by synthesis (SBS) chemistry.
Push-button apps in BaseSpace Sequence Hub simplify data analysis, so you can spend less time analyzing data and more time focusing on the next breakthrough.
Click on the below to view products for each workflow step.
An easy-to-use online software tool that provides dynamic feedback to optimize designs.TruSight Cancer Sequencing Panel
A fixed panel containing 94 genes and 284 SNPs associated with cancer predisposition.TruSight Tumor 15
Focused panel to assess relevant solid tumor somatic variants in a simple, sample-to-data workflow.TruSight Myeloid Sequencing Panel
A fixed panel targeting oncogenic exons and tumor suppressor genes for myeloid malignancies.
A fixed panel of somatic mutational hotspots in a broad spectrum of cancers.TruSeq Custom Amplicon v1.5
A fully customizable assay for high plexity pools, and long tiling applications.TruSeq Custom Amplicon Low Input
A fully customizable assay for low-input and formalin-fixed, paraffin-embedded (FFPE) DNA samples.Nextera Rapid Capture Custom Enrichment Kit
Customized probe design to target 0.5–25 Mb of custom content.
Simplest and most affordable solution for low-throughput targeted cancer sequencing.MiSeq System
Desktop sequencer featuring a simple NGS workflow, integrated data analysis software, and unmatched accuracy.
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.
The Illumina genomics computing environment for NGS data analysis and management.