Excalibur: A new ensemble method based on an optimal combination of aggregation tests for rare-variant association testing for sequencing data

Author:

Boutry SimonORCID,Helaers Raphaël,Lenaerts Tom,Vikkula MiikkaORCID

Abstract

The development of high-throughput next-generation sequencing technologies and large-scale genetic association studies produced numerous advances in the biostatistics field. Various aggregation tests, i.e. statistical methods that analyze associations of a trait with multiple markers within a genomic region, have produced a variety of novel discoveries. Notwithstanding their usefulness, there is no single test that fits all needs, each suffering from specific drawbacks. Selecting the right aggregation test, while considering an unknown underlying genetic model of the disease, remains an important challenge. Here we propose a new ensemble method, called Excalibur, based on an optimal combination of 36 aggregation tests created after an in-depth study of the limitations of each test and their impact on the quality of result. Our findings demonstrate the ability of our method to control type I error and illustrate that it offers the best average power across all scenarios. The proposed method allows for novel advances in Whole Exome/Genome sequencing association studies, able to handle a wide range of association models, providing researchers with an optimal aggregation analysis for the genetic regions of interest.

Funder

Fonds pour la Formation à la Recherche dans l’Industrie et dans l’Agriculture

Koning Boudewijnstichting

la Région wallonne dans le cadre du financement de l’axe stratégique FRFS-WELBIO

Université catholique de Louvain - Bourse Patrimoine

Publisher

Public Library of Science (PLoS)

Subject

Computational Theory and Mathematics,Cellular and Molecular Neuroscience,Genetics,Molecular Biology,Ecology,Modeling and Simulation,Ecology, Evolution, Behavior and Systematics

Reference102 articles.

1. 15 years of genome-wide association studies and no signs of slowing down;RJF Loos;Nature Communications,2020

2. The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog).;J MacArthur;Nucleic Acids Res,2017

3. High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells;Y Fu;Nat Biotechnol,2013

4. Methods for the Analysis and Interpretation for Rare Variants Associated with Complex Traits.;JD Weissenkampen;Curr Protoc Hum Genet,2019

5. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data;B Li;Am J Hum Genet,2008

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3