
NovaSeq X Series ordering
Advanced chemistry, optics, and informatics combine to deliver exceptional sequencing speed and data quality, outstanding throughput, and scalability.
This comprehensive, high-density microarray kit enables research into cancer predisposition and risk.
Data sheet PDF < 1 MB
Sample throughput
Number of markers
The Infinium OncoArray-500K contains 500,000 SNPs with a genome-wide backbone of 250,000 tag SNPs. Additional SNPs include genetic variants associated with breast, colorectal, lung, ovarian, and prostate cancers plus SNPs covering ancestry, quantitative traits, pharmacogenetics, and fine-mapping of common cancer susceptibility loci. To support additional research requirements, the Infinium OncoArray-500K can be tailored to incorporate up to 120,000 custom beadtypes.*
The Infinium OncoArray-500K was developed in collaboration with leading experts from the OncoArray consortium†, and draws on many of the features of the successful Collaborative Oncological Gene-environment Study (iCOGS) array1. Designed with candidate SNPs identified by the consortium, the OncoArray provides a cost-effective means to assess candidate variants potentially associated with cancer risk.
The Infinium OncoArray-500K uses a 24-sample high-throughput screening (HTS) BeadChip to enable maximum throughput, productivity, and genotyping accuracy. Using the proven iScan System, the Infinium OncoArray-500K is designed to combine affordability with high-density content, providing insight into the relationship between gene variants and cancer predisposition in five of the most prevalent cancers.
* For additional information about custom add-on content, contact your Illumina account manager or sales specialist.
Assay type | Infinium HTS |
---|---|
Automation capability | Automated array loader, Liquid handling robot(s) |
Input quantity | 200 ng |
Instruments | iScan System |
Method | Targeted genotyping array |
Nucleic acid type | DNA |
Number of markers |
Fixed markers: ~500,000 Custom marker add-on capacity: Up to 120,000 (with + kit versions) |
Sample throughput | ~2,304 samples per week |
Species category | Human |
Technology | Microarray |
Variant class | Single nucleotide polymorphisms (SNPs), Germline variants, Structural variants, Insertions-deletions (indels), Copy number variants (CNVs) |
Match your chosen kit size to the number of samples you run at a time. Each kit is processed as a single batch and is not designed to be divided across multiple experiments. If you are processing several low-throughput batches, order multiple small kits.
Germline Mutation Detection in Cancer
Identify germline mutations that predispose individuals to cancer using next-generation sequencing and microarrays.
Access a broad range of fixed and custom next-generation sequencing panels targeting known cancer-related gene variants.
Microarray Data Analysis & Experimental Design
Find microarray data analysis tools and tips to help you to visualize and analyze microarray data and facilitate data analysis for large experiments.
Technical note PDF < 1 MB
Technical note PDF 2 MB
Technical note PDF < 1 MB
Technical note PDF 2 MB
Data sheet PDF < 1 MB
Infinium OncoArray-500K BeadChip Kit (48 samples)
WG-355-1001
Each Infinium OncoArray-500K BeadChip can process twenty-fou...
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Infinium OncoArray-500K BeadChip Kit (288 samples)
WG-355-1002
Each Infinium OncoArray-500K BeadChip can process twenty-fou...
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Infinium OncoArray-500K v1.0 BeadChip Kit (1152 samples)
WG-355-1003
Each Infinium OncoArray-500K BeadChip can process twenty-fou...
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Infinium OncoArray-500K+ BeadChip Kit (48 samples)
WG-355-1011
Infinium OncoArray-500K+ v1.0 (48 samples)
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Infinium OncoArray-500K+ BeadChip Kit (288 samples)
WG-355-1012
Infinium OncoArray-500K+ v1.0 (288 samples)
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Infinium OncoArray-500K+ BeadChip Kit (1152 samples)
WG-355-1013
Infinium OncoArray-500K+ v1.0 (1152 samples)
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Advanced chemistry, optics, and informatics combine to deliver exceptional sequencing speed and data quality, outstanding throughput, and scalability.
Optimized reagent kit that provides increased cluster density and read length, improving sequencing quality scores compared to earlier versions.
Enable CGP with a large pan-cancer panel covering all major variant classes plus gene signatures (TMB, MSI, and HRD) from FFPE tissue.
A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.
Offers a 90-min workflow to prepare DNA libraries for small genomes, PCR amplicons, plasmids, and cDNA sequencing, with a low DNA input requirement.
A fully customizable microarray to interrogate virtually any target across any species to fit your unique study needs.
Infinium Exome-24 Kit arrays deliver exceptional coverage of putative functional exonic variants representing diverse populations and a range of common conditions.
BeadChip combining exceptional coverage of clinical research variants with optimized multiethnic, genome-wide content for genotype screening.
1. www.nature.com/icogs/primer/cogs-project-and-design-of-the-icogs-array
† The OncoArray consortium is an international collaboration of leading experts from the NCI-supported Genetic Association and Mechanisms in Oncology (GAME-ON) consortium, Genome Canada, Genome Quebec, and Cancer Research UK.
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