Literature DB >> 31307061

PRSice-2: Polygenic Risk Score software for biobank-scale data.

Shing Wan Choi1,2, Paul F O'Reilly1,2.   

Abstract

BACKGROUND: Polygenic risk score (PRS) analyses have become an integral part of biomedical research, exploited to gain insights into shared aetiology among traits, to control for genomic profile in experimental studies, and to strengthen causal inference, among a range of applications. Substantial efforts are now devoted to biobank projects to collect large genetic and phenotypic data, providing unprecedented opportunity for genetic discovery and applications. To process the large-scale data provided by such biobank resources, highly efficient and scalable methods and software are required.
RESULTS: Here we introduce PRSice-2, an efficient and scalable software program for automating and simplifying PRS analyses on large-scale data. PRSice-2 handles both genotyped and imputed data, provides empirical association P-values free from inflation due to overfitting, supports different inheritance models, and can evaluate multiple continuous and binary target traits simultaneously. We demonstrate that PRSice-2 is dramatically faster and more memory-efficient than PRSice-1 and alternative PRS software, LDpred and lassosum, while having comparable predictive power.
CONCLUSION: PRSice-2's combination of efficiency and power will be increasingly important as data sizes grow and as the applications of PRS become more sophisticated, e.g., when incorporated into high-dimensional or gene set-based analyses. PRSice-2 is written in C++, with an R script for plotting, and is freely available for download from http://PRSice.info.
© The Author(s) 2019. Published by Oxford University Press.

Entities:  

Keywords:  GWAS; imputation; polygenic risk score

Mesh:

Year:  2019        PMID: 31307061      PMCID: PMC6629542          DOI: 10.1093/gigascience/giz082

Source DB:  PubMed          Journal:  Gigascience        ISSN: 2047-217X            Impact factor:   6.524


  25 in total

1.  Polygenic Risk Scores That Predict Common Diseases Using Millions of Single Nucleotide Polymorphisms: Is More, Better?

Authors:  A Cecile JW Janssens; Michael J Joyner
Journal:  Clin Chem       Date:  2019-02-26       Impact factor: 8.327

2.  Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.

Authors:  Alicia R Martin; Christopher R Gignoux; Raymond K Walters; Genevieve L Wojcik; Benjamin M Neale; Simon Gravel; Mark J Daly; Carlos D Bustamante; Eimear E Kenny
Journal:  Am J Hum Genet       Date:  2017-03-30       Impact factor: 11.025

Review 3.  Genotype imputation.

Authors:  Yun Li; Cristen Willer; Serena Sanna; Gonçalo Abecasis
Journal:  Annu Rev Genomics Hum Genet       Date:  2009       Impact factor: 8.929

4.  Secondary use of clinical data: the Vanderbilt approach.

Authors:  Ioana Danciu; James D Cowan; Melissa Basford; Xiaoming Wang; Alexander Saip; Susan Osgood; Jana Shirey-Rice; Jacqueline Kirby; Paul A Harris
Journal:  J Biomed Inform       Date:  2014-02-14       Impact factor: 6.317

5.  Multi-polygenic score approach to trait prediction.

Authors:  E Krapohl; H Patel; S Newhouse; C J Curtis; S von Stumm; P S Dale; D Zabaneh; G Breen; P F O'Reilly; R Plomin
Journal:  Mol Psychiatry       Date:  2017-08-08       Impact factor: 15.992

6.  Multiethnic polygenic risk scores improve risk prediction in diverse populations.

Authors:  Carla Márquez-Luna; Po-Ru Loh; Alkes L Price
Journal:  Genet Epidemiol       Date:  2017-11-07       Impact factor: 2.135

7.  Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers.

Authors:  Karoline B Kuchenbaecker; Lesley McGuffog; Daniel Barrowdale; Andrew Lee; Penny Soucy; Joe Dennis; Susan M Domchek; Mark Robson; Amanda B Spurdle; Susan J Ramus; Nasim Mavaddat; Mary Beth Terry; Susan L Neuhausen; Rita Katharina Schmutzler; Jacques Simard; Paul D P Pharoah; Kenneth Offit; Fergus J Couch; Georgia Chenevix-Trench; Douglas F Easton; Antonis C Antoniou
Journal:  J Natl Cancer Inst       Date:  2017-07-01       Impact factor: 13.506

8.  Defining the role of common variation in the genomic and biological architecture of adult human height.

Authors:  Andrew R Wood; Tonu Esko; Jian Yang; Sailaja Vedantam; Tune H Pers; Stefan Gustafsson; Audrey Y Chu; Karol Estrada; Jian'an Luan; Zoltán Kutalik; Najaf Amin; Martin L Buchkovich; Damien C Croteau-Chonka; Felix R Day; Yanan Duan; Tove Fall; Rudolf Fehrmann; Teresa Ferreira; Anne U Jackson; Juha Karjalainen; Ken Sin Lo; Adam E Locke; Reedik Mägi; Evelin Mihailov; Eleonora Porcu; Joshua C Randall; André Scherag; Anna A E Vinkhuyzen; Harm-Jan Westra; Thomas W Winkler; Tsegaselassie Workalemahu; Jing Hua Zhao; Devin Absher; Eva Albrecht; Denise Anderson; Jeffrey Baron; Marian Beekman; Ayse Demirkan; Georg B Ehret; Bjarke Feenstra; Mary F Feitosa; Krista Fischer; Ross M Fraser; Anuj Goel; Jian Gong; Anne E Justice; Stavroula Kanoni; Marcus E Kleber; Kati Kristiansson; Unhee Lim; Vaneet Lotay; Julian C Lui; Massimo Mangino; Irene Mateo Leach; Carolina Medina-Gomez; Michael A Nalls; Dale R Nyholt; Cameron D Palmer; Dorota Pasko; Sonali Pechlivanis; Inga Prokopenko; Janina S Ried; Stephan Ripke; Dmitry Shungin; Alena Stancáková; Rona J Strawbridge; Yun Ju Sung; Toshiko Tanaka; Alexander Teumer; Stella Trompet; Sander W van der Laan; Jessica van Setten; Jana V Van Vliet-Ostaptchouk; Zhaoming Wang; Loïc Yengo; Weihua Zhang; Uzma Afzal; Johan Arnlöv; Gillian M Arscott; Stefania Bandinelli; Amy Barrett; Claire Bellis; Amanda J Bennett; Christian Berne; Matthias Blüher; Jennifer L Bolton; Yvonne Böttcher; Heather A Boyd; Marcel Bruinenberg; Brendan M Buckley; Steven Buyske; Ida H Caspersen; Peter S Chines; Robert Clarke; Simone Claudi-Boehm; Matthew Cooper; E Warwick Daw; Pim A De Jong; Joris Deelen; Graciela Delgado; Josh C Denny; Rosalie Dhonukshe-Rutten; Maria Dimitriou; Alex S F Doney; Marcus Dörr; Niina Eklund; Elodie Eury; Lasse Folkersen; Melissa E Garcia; Frank Geller; Vilmantas Giedraitis; Alan S Go; Harald Grallert; Tanja B Grammer; Jürgen Gräßler; Henrik Grönberg; Lisette C P G M de Groot; Christopher J Groves; Jeffrey Haessler; Per Hall; Toomas Haller; Goran Hallmans; Anke Hannemann; 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Serena Sanna; Hubert Scharnagl; Salome Scholtens; Fredrick R Schumacher; Heribert Schunkert; Robert A Scott; Joban Sehmi; Thomas Seufferlein; Jianxin Shi; Karri Silventoinen; Johannes H Smit; Albert Vernon Smith; Joanna Smolonska; Alice V Stanton; Kathleen Stirrups; David J Stott; Heather M Stringham; Johan Sundström; Morris A Swertz; Ann-Christine Syvänen; Bamidele O Tayo; Gudmar Thorleifsson; Jonathan P Tyrer; Suzanne van Dijk; Natasja M van Schoor; Nathalie van der Velde; Diana van Heemst; Floor V A van Oort; Sita H Vermeulen; Niek Verweij; Judith M Vonk; Lindsay L Waite; Melanie Waldenberger; Roman Wennauer; Lynne R Wilkens; Christina Willenborg; Tom Wilsgaard; Mary K Wojczynski; Andrew Wong; Alan F Wright; Qunyuan Zhang; Dominique Arveiler; Stephan J L Bakker; John Beilby; Richard N Bergman; Sven Bergmann; Reiner Biffar; John Blangero; Dorret I Boomsma; Stefan R Bornstein; Pascal Bovet; Paolo Brambilla; Morris J Brown; Harry Campbell; Mark J Caulfield; Aravinda Chakravarti; Rory Collins; 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Philippe Froguel; Leif C Groop; Christopher A Haiman; Anders Hamsten; M Geoffrey Hayes; Jennie Hui; David J Hunter; Kristian Hveem; J Wouter Jukema; Robert C Kaplan; Mika Kivimaki; Diana Kuh; Markku Laakso; Yongmei Liu; Nicholas G Martin; Winfried März; Mads Melbye; Susanne Moebus; Patricia B Munroe; Inger Njølstad; Ben A Oostra; Colin N A Palmer; Nancy L Pedersen; Markus Perola; Louis Pérusse; Ulrike Peters; Joseph E Powell; Chris Power; Thomas Quertermous; Rainer Rauramaa; Eva Reinmaa; Paul M Ridker; Fernando Rivadeneira; Jerome I Rotter; Timo E Saaristo; Danish Saleheen; David Schlessinger; P Eline Slagboom; Harold Snieder; Tim D Spector; Konstantin Strauch; Michael Stumvoll; Jaakko Tuomilehto; Matti Uusitupa; Pim van der Harst; Henry Völzke; Mark Walker; Nicholas J Wareham; Hugh Watkins; H-Erich Wichmann; James F Wilson; Pieter Zanen; Panos Deloukas; Iris M Heid; Cecilia M Lindgren; Karen L Mohlke; Elizabeth K Speliotes; Unnur Thorsteinsdottir; Inês Barroso; Caroline S Fox; Kari E North; David P Strachan; Jacques S Beckmann; Sonja I Berndt; Michael Boehnke; Ingrid B Borecki; Mark I McCarthy; Andres Metspalu; Kari Stefansson; André G Uitterlinden; Cornelia M van Duijn; Lude Franke; Cristen J Willer; Alkes L Price; Guillaume Lettre; Ruth J F Loos; Michael N Weedon; Erik Ingelsson; Jeffrey R O'Connell; Goncalo R Abecasis; Daniel I Chasman; Michael E Goddard; Peter M Visscher; Joel N Hirschhorn; Timothy M Frayling
Journal:  Nat Genet       Date:  2014-10-05       Impact factor: 38.330

9.  Shared genetic aetiology between cognitive functions and physical and mental health in UK Biobank (N=112 151) and 24 GWAS consortia.

Authors:  S P Hagenaars; S E Harris; G Davies; W D Hill; D C M Liewald; S J Ritchie; R E Marioni; C Fawns-Ritchie; B Cullen; R Malik; B B Worrall; C L M Sudlow; J M Wardlaw; J Gallacher; J Pell; A M McIntosh; D J Smith; C R Gale; I J Deary
Journal:  Mol Psychiatry       Date:  2016-01-26       Impact factor: 15.992

10.  Association of Polygenic Risk for Attention-Deficit/Hyperactivity Disorder With Co-occurring Traits and Disorders.

Authors:  Ebba Du Rietz; Jonathan Coleman; Kylie Glanville; Shing Wan Choi; Paul F O'Reilly; Jonna Kuntsi
Journal:  Biol Psychiatry Cogn Neurosci Neuroimaging       Date:  2017-12-14
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  232 in total

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2.  Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.

Authors:  Lam O Huang; Alexander Rauch; Eugenia Mazzaferro; Michael Preuss; Stefania Carobbio; Cigdem S Bayrak; Nathalie Chami; Zhe Wang; Ursula M Schick; Nancy Yang; Yuval Itan; Antonio Vidal-Puig; Marcel den Hoed; Susanne Mandrup; Tuomas O Kilpeläinen; Ruth J F Loos
Journal:  Nat Metab       Date:  2021-02-22

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Authors:  Aditya Ambati; Ryan Hillary; Smaranda Leu-Semenescu; Hanna M Ollila; Ling Lin; Emmanuel H During; Neal Farber; Thomas J Rico; Juliette Faraco; Eileen Leary; Andrea N Goldstein-Piekarski; Yu-Shu Huang; Fang Han; Yakov Sivan; Michel Lecendreux; Pauline Dodet; Makoto Honda; Natan Gadoth; Sona Nevsimalova; Fabio Pizza; Takashi Kanbayashi; Rosa Peraita-Adrados; Guy D Leschziner; Rosa Hasan; Francesca Canellas; Kazuhiko Kume; Makrina Daniilidou; Patrice Bourgin; David Rye; José L Vicario; Birgit Hogl; Seung Chul Hong; Guiseppe Plazzi; Geert Mayer; Anne Marie Landtblom; Yves Dauvilliers; Isabelle Arnulf; Emmanuel Jean-Marie Mignot
Journal:  Proc Natl Acad Sci U S A       Date:  2021-03-23       Impact factor: 11.205

4.  An Improved Genome-Wide Polygenic Score Model for Predicting the Risk of Type 2 Diabetes.

Authors:  Wei Liu; Zhenhuang Zhuang; Wenxiu Wang; Tao Huang; Zhonghua Liu
Journal:  Front Genet       Date:  2021-02-11       Impact factor: 4.599

5.  Making the Most of Clumping and Thresholding for Polygenic Scores.

Authors:  Florian Privé; Bjarni J Vilhjálmsson; Hugues Aschard; Michael G B Blum
Journal:  Am J Hum Genet       Date:  2019-11-21       Impact factor: 11.025

6.  A principal component approach to improve association testing with polygenic risk scores.

Authors:  Brandon J Coombes; Alexander Ploner; Sarah E Bergen; Joanna M Biernacka
Journal:  Genet Epidemiol       Date:  2020-07-21       Impact factor: 2.135

7.  The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls.

Authors:  Jonathan R I Coleman; Héléna A Gaspar; Julien Bryois; Gerome Breen
Journal:  Biol Psychiatry       Date:  2019-11-01       Impact factor: 13.382

8.  The impact of parenting a child with serious mental illness: Accounting for the parent's genetic vulnerability to mental illness.

Authors:  Jan Greenberg; Emily C Hilton; James J Li; Qiongshi Lu; Marsha R Mailick
Journal:  J Fam Psychol       Date:  2020-07-16

9.  Estimating genetic nurture with summary statistics of multigenerational genome-wide association studies.

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10.  Causal Associations Between Modifiable Risk Factors and the Alzheimer's Phenome.

Authors:  Shea J Andrews; Brian Fulton-Howard; Paul O'Reilly; Edoardo Marcora; Alison M Goate
Journal:  Ann Neurol       Date:  2020-10-15       Impact factor: 10.422

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