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Estimating disorder probability based on polygenic prediction using the BPC approach.

Emil Uffelmann1, ,

  • 1Department of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands. e.uffelmann@vu.nl.

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We developed a new Bayesian polygenic score Probability Conversion (BPC) method to accurately predict disorder probabilities. This approach improves genetic risk prediction for clinical use in binary traits.

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Area of Science:

  • Genetics
  • Statistical genetics
  • Bioinformatics

Background:

  • Polygenic Scores (PGSs) estimate genetic predisposition for traits.
  • Existing Bayesian PGS methods lack calibration for binary disorder traits in ascertained samples, hindering clinical use.
  • Accurate calibration is crucial for implementing PGSs in healthcare settings.

Purpose of the Study:

  • To introduce the Bayesian polygenic score Probability Conversion (BPC) approach.
  • To provide a practical method for computing well-calibrated disorder probabilities using PGSs.
  • To improve the accuracy of genetic risk prediction for binary traits.

Main Methods:

  • The BPC approach utilizes genome-wide association study summary statistics, existing Bayesian PGS methods (e.g., PRScs, SBayesR), and individual genotype data.
  • It incorporates a flexible prior disorder probability, adaptable from various sources.
  • The method does not require a separate tuning sample with both genotype and phenotype data.

Main Results:

  • BPC yields well-calibrated disorder probability predictions.
  • The approach demonstrates consistently superior performance compared to another recent method.
  • Validation was performed using simulated data and empirical data across nine disorder traits.

Conclusions:

  • The BPC approach offers a practical and effective solution for calibrating PGSs for binary disorder traits.
  • It enhances the reliability of genetic risk prediction, paving the way for clinical implementation.
  • BPC improves upon existing methods, providing more accurate and trustworthy genetic insights.