Targeted to comprehensive
Deliver comprehensive genomic insights with choices ranging from targeted amplicon-based panels optimized for limited input samples to large hybrid-capture panels.
Transform oncology research with Illumina genomic solutions
Unlock deeper cancer biology and insights
From sample to discovery with confidence
Illumina offers a comprehensive portfolio of oncology research workflow solutions designed to help laboratories generate high-quality, reproducible genomic insights across a broad range of cancer research applications. By integrating trusted assays, scalable sequencing platforms, and advanced data analysis, Illumina enables researchers to move efficiently from sample to discovery with confidence.
The Illumina oncology research genomic ecosystem is among the most trusted in the world. Our integrated, sample-to-data solutions reduce workflow complexity while delivering the flexibility and scalability required to support evolving research needs. This unified approach enables consistent, high-quality results that accelerate the discovery and analysis of cancer-related variants.
Portfolio breadth and flexibility
The Illumina oncology research next-generation sequencing (NGS) portfolio continues to expand to analyze a wide range of sample types, inputs, and biomarker content within a consistent workflow framework. These capabilities empower oncology researchers to study cancer biology with greater depth, consistency, and confidence.
Rapid workflows for oncology research
The NGS workflow for oncology research applications offers a rapid sample-to-report solution.
Prepare
Innovative sample preparation
Illumina library prep kits offer future-proof content and flexibility across sample input types and throughput requirements, supporting a wide range of research and applied sequencing needs.
Automation-ready kits enable optimized liquid handling to reduce manual steps, improve consistency, and maximize lab efficiency as demand scales.
Sequence
Recognized sequencing power
Powered by proven NGS technology and industry-leading SBS chemistry, Illumina sequencing systems provide a trusted foundation for high-performance sequencing across applications and scales.
Our comprehensive portfolio of sequencing platforms delivers scalable solutions designed to adapt as your needs evolve.
Analyze
Reliable data sooner
DRAGEN delivers accurate, comprehensive, and efficient secondary analysis of NGS data across both local and cloud environments.
Connected tertiary analysis leverages extensive knowledge sources to streamline variant interpretation and accelerate insights with fewer touchpoints.
Oncology research genomic portfolio workflow solutions
Illumina offers genomic workflow solutions for oncology research that take you from sample to discovery.
Prepare
Pillar oncoReveal panelsTargeted sequencing technology from Pillar Biosciences alongside Illumina sequencing and bioinformatics solutions enables rapid and focused genomic profiling of solid organ and hematologic cancers.
Sequence
MiSeq i100A benchtop system offering simple setup, short run times, scalable output, and exceptional data quality.
NextSeq 550A benchtop, mid-throughput system with load-and-go reagents.
NextSeq 1000/2000A benchtop, mid-throughput system that drives costs down and minimizes waste with XLEAP-SBS.
Analyze
DRAGEN Secondary AnalysisDRAGEN analysis offers accurate, comprehensive, and efficient secondary analysis of NGS data available on both local and cloud-based systems.
Connected Insights Tertiary AnalysisConnected Insights analysis offers comprehensive insights and automation to support somatic oncology variant interpretation and research reporting for any assay, at any scale.
Prepare
TruSight Oncology 500 v2Enables CGP with a large pan-cancer panel with variants and key biomarkers from FFPE tissue.
TruSight Oncology 500 ctDNA v2Use minimally invasive blood samples to assess circulating tumor DNA (ctDNA).
Library Prep AutomationTSO 500 library prep automation kits are formulated for use with liquid handling robots, providing optimized volumes to maximize lab efficiency.
Sequence
NextSeq 550A benchtop, mid-throughput system with load-and-go reagents.
NextSeq 1000/2000A benchtop, mid-throughput system that drives costs down and minimizes waste with XLEAP-SBS.
Analyze
DRAGEN Secondary AnalysisAccurate, comprehensive, and efficient secondary analysis of NGS data across local and cloud-based systems.
Connected Insights Tertiary AnalysisComprehensive insights and automation for somatic oncology variant interpretation and research reporting.
* XLEAP-SBS chemistry is an even faster, higher quality, and more robust version of proven sequencing by synthesis chemistry.
Application and customer insights
Targeted oncology research workflow with Pillar oncoReveal
Rapid, accurate results with oncoReveal panels on MiSeq i100 Series, analyzed and reported with DRAGEN Amplicon and Illumina Connected Insights.
TruSight Oncology 500 portfolio
TSO 500 library prep automation kits are formulated for use with liquid handling robots, providing optimized volumes to maximize lab efficiency.
Connect with ERMRI
Contact our team to learn more about oncology research workflow solutions and how to apply the right genomic approach for your project.
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