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sumSTAAR: A flexible framework for gene-based association studies using GWAS summary statistics
Gene-based association analysis is an effective gene-mapping tool. Many gene-based methods have been proposed recently. However, their power depends on the underlying genetic architecture, which is rarely known in complex traits, and so it is likely that a combination of such methods could serve as...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197066/ https://www.ncbi.nlm.nih.gov/pubmed/35653402 http://dx.doi.org/10.1371/journal.pcbi.1010172 |
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author | Belonogova, Nadezhda M. Svishcheva, Gulnara R. Kirichenko, Anatoly V. Zorkoltseva, Irina V. Tsepilov, Yakov A. Axenovich, Tatiana I. |
author_facet | Belonogova, Nadezhda M. Svishcheva, Gulnara R. Kirichenko, Anatoly V. Zorkoltseva, Irina V. Tsepilov, Yakov A. Axenovich, Tatiana I. |
author_sort | Belonogova, Nadezhda M. |
collection | PubMed |
description | Gene-based association analysis is an effective gene-mapping tool. Many gene-based methods have been proposed recently. However, their power depends on the underlying genetic architecture, which is rarely known in complex traits, and so it is likely that a combination of such methods could serve as a universal approach. Several frameworks combining different gene-based methods have been developed. However, they all imply a fixed set of methods, weights and functional annotations. Moreover, most of them use individual phenotypes and genotypes as input data. Here, we introduce sumSTAAR, a framework for gene-based association analysis using summary statistics obtained from genome-wide association studies (GWAS). It is an extended and modified version of STAAR framework proposed by Li and colleagues in 2020. The sumSTAAR framework offers a wider range of gene-based methods to combine. It allows the user to arbitrarily define a set of these methods, weighting functions and probabilities of genetic variants being causal. The methods used in the framework were adapted to analyse genes with large number of SNPs to decrease the running time. The framework includes the polygene pruning procedure to guard against the influence of the strong GWAS signals outside the gene. We also present new improved matrices of correlations between the genotypes of variants within genes. These matrices estimated on a sample of 265,000 individuals are a state-of-the-art replacement of widely used matrices based on the 1000 Genomes Project data. |
format | Online Article Text |
id | pubmed-9197066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-91970662022-06-15 sumSTAAR: A flexible framework for gene-based association studies using GWAS summary statistics Belonogova, Nadezhda M. Svishcheva, Gulnara R. Kirichenko, Anatoly V. Zorkoltseva, Irina V. Tsepilov, Yakov A. Axenovich, Tatiana I. PLoS Comput Biol Research Article Gene-based association analysis is an effective gene-mapping tool. Many gene-based methods have been proposed recently. However, their power depends on the underlying genetic architecture, which is rarely known in complex traits, and so it is likely that a combination of such methods could serve as a universal approach. Several frameworks combining different gene-based methods have been developed. However, they all imply a fixed set of methods, weights and functional annotations. Moreover, most of them use individual phenotypes and genotypes as input data. Here, we introduce sumSTAAR, a framework for gene-based association analysis using summary statistics obtained from genome-wide association studies (GWAS). It is an extended and modified version of STAAR framework proposed by Li and colleagues in 2020. The sumSTAAR framework offers a wider range of gene-based methods to combine. It allows the user to arbitrarily define a set of these methods, weighting functions and probabilities of genetic variants being causal. The methods used in the framework were adapted to analyse genes with large number of SNPs to decrease the running time. The framework includes the polygene pruning procedure to guard against the influence of the strong GWAS signals outside the gene. We also present new improved matrices of correlations between the genotypes of variants within genes. These matrices estimated on a sample of 265,000 individuals are a state-of-the-art replacement of widely used matrices based on the 1000 Genomes Project data. Public Library of Science 2022-06-02 /pmc/articles/PMC9197066/ /pubmed/35653402 http://dx.doi.org/10.1371/journal.pcbi.1010172 Text en © 2022 Belonogova et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Belonogova, Nadezhda M. Svishcheva, Gulnara R. Kirichenko, Anatoly V. Zorkoltseva, Irina V. Tsepilov, Yakov A. Axenovich, Tatiana I. sumSTAAR: A flexible framework for gene-based association studies using GWAS summary statistics |
title | sumSTAAR: A flexible framework for gene-based association studies using GWAS summary statistics |
title_full | sumSTAAR: A flexible framework for gene-based association studies using GWAS summary statistics |
title_fullStr | sumSTAAR: A flexible framework for gene-based association studies using GWAS summary statistics |
title_full_unstemmed | sumSTAAR: A flexible framework for gene-based association studies using GWAS summary statistics |
title_short | sumSTAAR: A flexible framework for gene-based association studies using GWAS summary statistics |
title_sort | sumstaar: a flexible framework for gene-based association studies using gwas summary statistics |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197066/ https://www.ncbi.nlm.nih.gov/pubmed/35653402 http://dx.doi.org/10.1371/journal.pcbi.1010172 |
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