Screenshot

BridgePRS is a Bayesian method that utilises ridge regression developed to tackle the "PRS Portability Problem". The PRS portability problem causes lower PRS accuracy in target populations not included in the GWAS base used to estimate the PRS. This is due to differences in linkage disequilibrium (LD), allele frequency and gene–environment interactions affecting causal effect sizes between the base and target populations.

Download Links

BridgePRS Software Packages
OS Link Last Updated
Linux 64-Bit v1.0.3 9-13-2024
Mac 64-Bit v1.0.3 9-10-2024
Windows NA Not Available

1000G genotype data from the five super-populations (AFR, AMR, EAS, EUR, SAS) is provided to estimate LD in BridgePRS analyses for three SNP sets: HapMap Variants, 1000G variants with MAF>5% in any one of the five 1000G super-populations, 1000G variants with MAF>1% in one any of the five 1000G super-populations: |Reference Panels | |--| |

Download Link Size More Information
HapMap Variants <1GB International HapMap Project
1000 Genomes: MAF>5% 8GB IGSR Website
1000 Genomes: MAF>1% 14GB IGSR Website

Trouble Downloading Ref Panels?

Latest Updates

2024-11-02 (v0.1.7)

  • Added a direct downloads page for users who have trouble downloading large reference panels.
  • Added sample thousand genomes data.
  • update log can be found here

Overview

  • BridgePRS is written in R with a Python wrapper. Plink. is used in the first stage of the modelling for clumping and thresholding (all markers within clumps are retained for analysis). For more information on installing dependencies, please refer to Requirements.
  • To get BridgePRS running using toy data see our Quick Start Tutorial..
  • Following the Quick Start, the full guide provides more realistic examples to help you get started with your own data.

Citation: Our Manuscript is published in Nature Genetics

Please cite our paper:

Hoggart C, Choi SW, García-González J, Souaiaia T, Preuss M, O'Reilly P. BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. Nat Genet 56, 180–186 (2024). https://doi.org/10.1038/s41588-023-01583-9

Contact

For questions about the methodology, this website, or our manuscript please contact Dr Clive Hoggart, Dr Tade Souaiaia, or Dr Paul O'Reilly. For source code and coding issues please visit the bridgePRS github here.

Acknowledgements

We would like to thank Brian Fulton-Howard for his feedback and help with testing.