View the release notes for more information and supported Polygenic Risk Scores.
Polygenic Risk Score software–Predict module
Illumina Polygenic Risk Score (PRS) software enables simplified analysis and reporting.
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Product Highlights
Illumina Polygenic Risk Score software is a user-friendly research solution that accelerates the complex Polygenic Risk Score (PRS) development process while reducing the need for technical expertise.
The Predict module identifies an individual's genetic disease risk, considering their ancestral background. The Predict module uses imputation software to increase the number of genetic variants included in your dataset. This allows you to apply your risk score or choose from a list of risk scores from the Polygenic Score Catalog (PGS Catalog). The output is an optional summary report of an individual’s risk score compared to a reference population, allowing you to estimate any variance in relative risk.
The Illumina Polygenic Risk Score software – Predict module offers:
- Streamlined genotype-to-risk assessment with broad disorder coverage
- An easy-to-use interface for simplified data analysis and PRS reporting
- Ancestry-informed genetic risk scores for highly accurate disease risk prediction
Frequently Purchased Together
Case Studies
Polygenic Risk Scores Could Become Useful Tools in the Physician's Toolbox
Researchers perform large genome-wide association studies with the Global Screening Array to identify disease-associated DNA risk loci and develop PRSs for clinical validation.
Read MoreSimplified workflow for PRS determination using the Predict module. The Predict module offers a comprehensive risk prediction solution for fast and accurate disease risk assessments without the need for extensive bioinformatics resources.
In BaseSpace Sequence Hub, navigate to ‘Runs - Microarray Analysis Setup’ to get started with analysis
Setup analysis configuration including PRS selection
Select sample for analysis with Sample Sheet or BeadChips
View analysis results
Polygenic Risk Score report - Individualized reports convey the relative risk percentile for each sample in an easy-to-visualize format with information about the PRS that was used for risk calculation.
Product Literature
Data Sheet | PDF | 6 versions
Manuals and Support Information
Infinium Global Diversity Array-8 Kit
The Global Diversity Array-8 (GDA) BeadChip combines exceptional coverage of clinical research variants with optimized multi-ethnic, genome-wide content.
Infinium Global Screening Array-24 Kit
This next-generation genotyping array provides a scalable, cost-effective solution for population genetics, pharmacogenomics studies, and precision medicine research.
BaseSpace Sequence Hub
Data management and simplified bioinformatics for labs getting started and for rapidly scaling next-generation sequencing (NGS) operations.