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Microarray Systems

From cytogenetics to population-scale genotyping

Explore complete microarray solutions that your lab needs.
We provide a broad portfolio of high-performance platforms and panels tailored for clinical, research, and agricultural genomics applications.

Unlock performance and flexibility in your lab with iSCAN™

Boost your microarray performance with a system that can support a variety of applications, such as biomarker screening, DNA methylation research, and agrigenomics. The iScan System is flexible enough to accommodate different throughput requirements while providing high-quality data for a wide range of genomic applications.
Genotyping

Genotyping

Methylation

Methylation

Cytogenomics

Cytogenomics

1.25

min

Average scan time per sample

30

min

Average scan time per beadchip

5670

Maximum weekly throughput

The iSCANTM System Specifications

Parameter
Specification
Pixel resolution
0.53 µm
Laser excitation
532 nm and 658 nm dual-laser excitation
Image file output
TIFF or JPG data file output with automatic image quality analysis (uncompressed or compressed)
System dimensions (W × H × D)
52 cm × 45 cm × 66 cm
Air table dimensions (W × H × D)
61 cm × 6 cm × 69 cm
Weight
65 kg (143 lbs)
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Scalable charging solutions that grows with you.

Plant and Animal Genomics

Use genotyping and NGS technologies to better understand the genetic variation driving key traits in plants and animals.

Commercial Agriculture

Enable efficient breeding decisions using tools for trait screening, backcrossing, and parentage testing, all powered by agrigenomics.

Agriculture Consortia & Community

Work within global consortia to co-develop solutions and contribute to agricultural progress addressing hunger, malnutrition, and sustainability.

Perform a Deep Screening Your Cytogenetic Analysis

Illumina Infinium™ Global Screening Array with Cytogenetics enables high-sensitivity analysis of structural variants such as chromosomal imbalances, deletions and duplications.

This solution, specifically optimised for clinical cytogenetic applications, enhances diagnostic reliability with genome-wide CNV and LoH detection.3

Infinium™ Global Screening Array with Cytogenetics

Find Solutions That Are Tailored for Your Needs
with Global Diversity Array.

Focused on capturing ethnic diversity in order to accelerate disease research and treatments.​

Focused on capturing ethnic diversity in order to accelerate disease research and treatments.​

Designed for discovery and polygenic risk score development in multi-ethnic and mixed populations.​

Designed for discovery and polygenic risk score development in multi-ethnic and mixed populations.​

Includes the updated content of the ACMG 59 panel and the structural variants defined by Audano et al. (2019).​

Includes the updated content of the ACMG 59 panel and the structural variants defined by Audano et al. (2019).​

Includes enhanced exome coverage for the identification of high-impact variants.​

Includes enhanced exome coverage for the identification of high-impact variants.​

Current clinical research and quality control content is available for screening and sample tracking.​

Current clinical research and quality control content is available for screening and sample tracking.​

It contains Carrier Screening (CS) and Polygenic Risk Score (PRS) arrays specifically designed for the GDA backbone.​

It contains Carrier Screening (CS) and Polygenic Risk Score (PRS) arrays specifically designed for the GDA backbone.​

Global Diversity Array

Carrier Screening

Illumina Infinium™ Global Diversity Array with Carrier Screening Content

Polygenic Risk Score

Illumina Infinium™ Global Diversity Array with Polygenic Risk Score Content

Prevent Risks with Expanded Carrier Screening

Includes 45,000 variants specific to carrier screening covering 602 genes.

Includes 45,000 variants specific to carrier screening covering 602 genes.

Provides 97% coverage for diseases occurring at a frequency of 1/200 or higher.

Provides 97% coverage for diseases occurring at a frequency of 1/200 or higher.

Includes all ACMG recommended tier 1-3 carrier genes (except FMR1 and FXN).

Includes all ACMG recommended tier 1-3 carrier genes (except FMR1 and FXN).

Identifies both sequence and structural variants by integrating different workflows into a single analysis.

Identifies both sequence and structural variants by integrating different workflows into a single analysis.

Infinium™ Global Diversity Array with Carrier Screening Content

Stay Ahead with Polygenic Risk Score Analysis

Microarray Systems
Genetic factors and associated PRS
Microarray Systems
Environmental Factors and Lifestyle
Microarray Systems
Overall Complex Disease Risk

The polygenic risk score (PRS) is an estimate of an individual’s genetic susceptibility to a trait or disease, calculated based on their genotype profile and relevant genome-wide association study (GWAS) data.

PRS calculation is performed using panels containing different numbers of single-nucleotide polymorphisms (SNPs). For each SNP, the sum of risk alleles is calculated by weighting them with the corresponding effect size.

SNPs and their corresponding effect sizes are obtained from the largest GWAS available for the relevant disease.

A versatile, scalable platform for multi-ethnic PRS research

  • 1.3 Million SNP backbone with 160K PRS Markers
  • Highly accurate, pan-ethnic PRS estimation
  • Predict for automated analysis
  • Analysis of over 20 traits in a single study
Infinium™ Global Diversity Array with Polygenic Risk Score Content