Genetic tests to determine risk for monogenic diseases (such as cystic fibrosis or Huntington’s Disease) that are caused by a single mutation have been in use for over a decade. However, determining risk for complex diseases, which can be caused by hundreds to thousands of genetic variants that act in conjunction with environmental factors, remains challenging.
Polygenic risk scores (also known as polygenic scores and genetic risk scores; PRS) represent the total number of genetic variants that an individual has to assess their heritable risk of developing a particular disease. While there is still much more work needed to realize the potential for polygenic risk scores in precision medicine, polygenic risk scores have the potential to impact complex disease research and healthcare in a variety of ways:
Explore ways to customize your genotyping assays.
A comprehensive, high-performance solution to analyze polygenic risk scores.
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Perform reliable, high-throughput scanning for a wide range of applications.
User-friendly, point-and-click software accelerates the PRS implementation process.
Explore how polygenic risk scores are developed, from design to validation, and learn which additional reporting and quality aspects to consider for your research.View App Note
Polygenic risk scores can provide researchers valuable insight into how predictive biomarkers for a specific complex disease can stratify populations according to risk. A study published by Khera, et al. in 2018 examined genome-wide polygenic risk scores in a population of over 250,000 individuals in the UK Biobank.1 They found 8% of the population tested had polygenic risk scores that conferred ≥ threefold increased risk for coronary artery disease.
In the first chapter of this series, experts explain what a polygenic risk score is and how they’re relevant to complex diseases.
Geneticists share key considerations researchers should think about when developing a polygenic risk score.
Learn more about future uses for polygenic risk scores, from stratifying populations to early intervention and preventative medicine.
Watch leading geneticists and professors share their insights about how polygenic risk scores can be used to predict an individual’s risk of complex disease.
Researchers perform genome-wide association studies to identify disease-associated DNA risk loci and develop scores for clinical validation.
Polygenic risk scores summarize genome-wide genotype data into a single number that represents genetic liability to a trait. Read this guide to learn more.
In this on-demand webinar, Dr. Estelle Giraud provides an overview on Polygenic Risk Scores (PRS), why they are clinically relevant and how they may be used in the future.
Similar to polygenic risk scores, the field of pharmacogenomics benefits from genome-wide association studies to predict an individual’s response or ability to metabolize a drug or therapeutic. These studies provide valuable insights and have the potential to allow for tailored medications and dosages for patients.
Learn how GWAS can find genetic variants for traits or disease through high-throughput technologies.
Read about genotyping methods to help you better understand diseases at the molecular level.
Explore how SNP and SNV can provide insights into disease or important phenotypes.
Read more about how a comprehensive view of the genome enables efficient discovery of important variants and novel genome assembly.
Discover how the power of next-generation sequencing (NGS) can reveal genomic and transcriptomic information in a scalable and high-throughput format.