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Genotype imputation and variability in polygenic risk score estimation

BACKGROUND: Polygenic risk scores (PRSs) are a summarization of an individual’s genetic risk for a disease or trait. These scores are being generated in research and commercial settings to study how they may be used to guide healthcare decisions. PRSs should be updated as genetic knowledgebases impr...

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Autores principales: Chen, Shang-Fu, Dias, Raquel, Evans, Doug, Salfati, Elias L., Liu, Shuchen, Wineinger, Nathan E., Torkamani, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682022/
https://www.ncbi.nlm.nih.gov/pubmed/33225976
http://dx.doi.org/10.1186/s13073-020-00801-x
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author Chen, Shang-Fu
Dias, Raquel
Evans, Doug
Salfati, Elias L.
Liu, Shuchen
Wineinger, Nathan E.
Torkamani, Ali
author_facet Chen, Shang-Fu
Dias, Raquel
Evans, Doug
Salfati, Elias L.
Liu, Shuchen
Wineinger, Nathan E.
Torkamani, Ali
author_sort Chen, Shang-Fu
collection PubMed
description BACKGROUND: Polygenic risk scores (PRSs) are a summarization of an individual’s genetic risk for a disease or trait. These scores are being generated in research and commercial settings to study how they may be used to guide healthcare decisions. PRSs should be updated as genetic knowledgebases improve; however, no guidelines exist for their generation or updating. METHODS: Here, we characterize the variability introduced in PRS calculation by a common computational process used in their generation—genotype imputation. We evaluated PRS variability when performing genotype imputation using 3 different pre-phasing tools (Beagle, Eagle, SHAPEIT) and 2 different imputation tools (Beagle, Minimac4), relative to a WGS-based gold standard. Fourteen different PRSs spanning different disease architectures and PRS generation approaches were evaluated. RESULTS: We find that genotype imputation can introduce variability in calculated PRSs at the individual level without any change to the underlying genetic model. The degree of variability introduced by genotype imputation differs across algorithms, where pre-phasing algorithms with stochastic elements introduce the greatest degree of score variability. In most cases, PRS variability due to imputation is minor (< 5 percentile rank change) and does not influence the interpretation of the score. PRS percentile fluctuations are also reduced in the more informative tails of the PRS distribution. However, in rare instances, PRS instability at the individual level can result in singular PRS calculations that differ substantially from a whole genome sequence-based gold standard score. CONCLUSIONS: Our study highlights some challenges in applying population genetics tools to individual-level genetic analysis including return of results. Rare individual-level variability events are masked by a high degree of overall score reproducibility at the population level. In order to avoid PRS result fluctuations during updates, we suggest that deterministic imputation processes or the average of multiple iterations of stochastic imputation processes be used to generate and deliver PRS results. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-020-00801-x.
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spelling pubmed-76820222020-11-23 Genotype imputation and variability in polygenic risk score estimation Chen, Shang-Fu Dias, Raquel Evans, Doug Salfati, Elias L. Liu, Shuchen Wineinger, Nathan E. Torkamani, Ali Genome Med Research BACKGROUND: Polygenic risk scores (PRSs) are a summarization of an individual’s genetic risk for a disease or trait. These scores are being generated in research and commercial settings to study how they may be used to guide healthcare decisions. PRSs should be updated as genetic knowledgebases improve; however, no guidelines exist for their generation or updating. METHODS: Here, we characterize the variability introduced in PRS calculation by a common computational process used in their generation—genotype imputation. We evaluated PRS variability when performing genotype imputation using 3 different pre-phasing tools (Beagle, Eagle, SHAPEIT) and 2 different imputation tools (Beagle, Minimac4), relative to a WGS-based gold standard. Fourteen different PRSs spanning different disease architectures and PRS generation approaches were evaluated. RESULTS: We find that genotype imputation can introduce variability in calculated PRSs at the individual level without any change to the underlying genetic model. The degree of variability introduced by genotype imputation differs across algorithms, where pre-phasing algorithms with stochastic elements introduce the greatest degree of score variability. In most cases, PRS variability due to imputation is minor (< 5 percentile rank change) and does not influence the interpretation of the score. PRS percentile fluctuations are also reduced in the more informative tails of the PRS distribution. However, in rare instances, PRS instability at the individual level can result in singular PRS calculations that differ substantially from a whole genome sequence-based gold standard score. CONCLUSIONS: Our study highlights some challenges in applying population genetics tools to individual-level genetic analysis including return of results. Rare individual-level variability events are masked by a high degree of overall score reproducibility at the population level. In order to avoid PRS result fluctuations during updates, we suggest that deterministic imputation processes or the average of multiple iterations of stochastic imputation processes be used to generate and deliver PRS results. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-020-00801-x. BioMed Central 2020-11-23 /pmc/articles/PMC7682022/ /pubmed/33225976 http://dx.doi.org/10.1186/s13073-020-00801-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chen, Shang-Fu
Dias, Raquel
Evans, Doug
Salfati, Elias L.
Liu, Shuchen
Wineinger, Nathan E.
Torkamani, Ali
Genotype imputation and variability in polygenic risk score estimation
title Genotype imputation and variability in polygenic risk score estimation
title_full Genotype imputation and variability in polygenic risk score estimation
title_fullStr Genotype imputation and variability in polygenic risk score estimation
title_full_unstemmed Genotype imputation and variability in polygenic risk score estimation
title_short Genotype imputation and variability in polygenic risk score estimation
title_sort genotype imputation and variability in polygenic risk score estimation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682022/
https://www.ncbi.nlm.nih.gov/pubmed/33225976
http://dx.doi.org/10.1186/s13073-020-00801-x
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