RAISS: robust and accurate imputation from summary statistics

Abstract Motivation Multi-trait analyses using public summary statistics from genome-wide association studies (GWASs) are becoming increasingly popular. A constraint of multi-trait methods is that they require complete summary data for all traits. Although methods for the imputation of summary stati...

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Published inBioinformatics Vol. 35; no. 22; pp. 4837 - 4839
Main Authors Julienne, Hanna, Shi, Huwenbo, Pasaniuc, Bogdan, Aschard, Hugues
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.11.2019
Oxford University Press (OUP)
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ISSN1367-4803
1367-4811
1460-2059
1367-4811
DOI10.1093/bioinformatics/btz466

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Summary:Abstract Motivation Multi-trait analyses using public summary statistics from genome-wide association studies (GWASs) are becoming increasingly popular. A constraint of multi-trait methods is that they require complete summary data for all traits. Although methods for the imputation of summary statistics exist, they lack precision for genetic variants with small effect size. This is benign for univariate analyses where only variants with large effect size are selected a posteriori. However, it can lead to strong p-value inflation in multi-trait testing. Here we present a new approach that improve the existing imputation methods and reach a precision suitable for multi-trait analyses. Results We fine-tuned parameters to obtain a very high accuracy imputation from summary statistics. We demonstrate this accuracy for variants of all effect sizes on real data of 28 GWAS. We implemented the resulting methodology in a python package specially designed to efficiently impute multiple GWAS in parallel. Availability and implementation The python package is available at: https://gitlab.pasteur.fr/statistical-genetics/raiss, its accompanying documentation is accessible here http://statistical-genetics.pages.pasteur.fr/raiss/. Supplementary information Supplementary data are available at Bioinformatics online.
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ISSN:1367-4803
1367-4811
1460-2059
1367-4811
DOI:10.1093/bioinformatics/btz466