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LDpred2: better, faster, stronger
MOTIVATION: Polygenic scores have become a central tool in human genetics research. LDpred is a popular method for deriving polygenic scores based on summary statistics and a matrix of correlation between genetic variants. However, LDpred has limitations that may reduce its predictive performance. R...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016455/ https://www.ncbi.nlm.nih.gov/pubmed/33326037 http://dx.doi.org/10.1093/bioinformatics/btaa1029 |
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author | Privé, Florian Arbel, Julyan Vilhjálmsson, Bjarni J |
author_facet | Privé, Florian Arbel, Julyan Vilhjálmsson, Bjarni J |
author_sort | Privé, Florian |
collection | PubMed |
description | MOTIVATION: Polygenic scores have become a central tool in human genetics research. LDpred is a popular method for deriving polygenic scores based on summary statistics and a matrix of correlation between genetic variants. However, LDpred has limitations that may reduce its predictive performance. RESULTS: Here, we present LDpred2, a new version of LDpred that addresses these issues. We also provide two new options in LDpred2: a ‘sparse’ option that can learn effects that are exactly 0, and an ‘auto’ option that directly learns the two LDpred parameters from data. We benchmark predictive performance of LDpred2 against the previous version on simulated and real data, demonstrating substantial improvements in robustness and predictive accuracy compared to LDpred1. We then show that LDpred2 also outperforms other polygenic score methods recently developed, with a mean AUC over the 8 real traits analyzed here of 65.1%, compared to 63.8% for lassosum, 62.9% for PRS-CS and 61.5% for SBayesR. Note that LDpred2 provides more accurate polygenic scores when run genome-wide, instead of per chromosome. AVAILABILITY AND IMPLEMENTATION: LDpred2 is implemented in R package bigsnpr. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-8016455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-80164552021-04-07 LDpred2: better, faster, stronger Privé, Florian Arbel, Julyan Vilhjálmsson, Bjarni J Bioinformatics Original Papers MOTIVATION: Polygenic scores have become a central tool in human genetics research. LDpred is a popular method for deriving polygenic scores based on summary statistics and a matrix of correlation between genetic variants. However, LDpred has limitations that may reduce its predictive performance. RESULTS: Here, we present LDpred2, a new version of LDpred that addresses these issues. We also provide two new options in LDpred2: a ‘sparse’ option that can learn effects that are exactly 0, and an ‘auto’ option that directly learns the two LDpred parameters from data. We benchmark predictive performance of LDpred2 against the previous version on simulated and real data, demonstrating substantial improvements in robustness and predictive accuracy compared to LDpred1. We then show that LDpred2 also outperforms other polygenic score methods recently developed, with a mean AUC over the 8 real traits analyzed here of 65.1%, compared to 63.8% for lassosum, 62.9% for PRS-CS and 61.5% for SBayesR. Note that LDpred2 provides more accurate polygenic scores when run genome-wide, instead of per chromosome. AVAILABILITY AND IMPLEMENTATION: LDpred2 is implemented in R package bigsnpr. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2020-12-16 /pmc/articles/PMC8016455/ /pubmed/33326037 http://dx.doi.org/10.1093/bioinformatics/btaa1029 Text en © The Author(s) 2020. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Privé, Florian Arbel, Julyan Vilhjálmsson, Bjarni J LDpred2: better, faster, stronger |
title | LDpred2: better, faster, stronger |
title_full | LDpred2: better, faster, stronger |
title_fullStr | LDpred2: better, faster, stronger |
title_full_unstemmed | LDpred2: better, faster, stronger |
title_short | LDpred2: better, faster, stronger |
title_sort | ldpred2: better, faster, stronger |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016455/ https://www.ncbi.nlm.nih.gov/pubmed/33326037 http://dx.doi.org/10.1093/bioinformatics/btaa1029 |
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