HAPNEST: efficient, large-scale generation and evaluation of synthetic datasets for genotypes and phenotypes

Author:

Wharrie Sophie1ORCID,Yang Zhiyu2,Raj Vishnu1,Monti Remo3,Gupta Rahul4,Wang Ying4,Martin Alicia4ORCID,O’Connor Luke J4,Kaski Samuel15,Marttinen Pekka1,Palamara Pier Francesco6ORCID,Lippert Christoph37ORCID,Ganna Andrea24

Affiliation:

1. Department of Computer Science, Aalto University , Espoo 02150, Finland

2. Institute for Molecular Medicine Finland, FIMM, HiLIFE, University of Helsinki , Helsinki 00014, Finland

3. Hasso Plattner Institute, University of Potsdam, Digital Engineering Faculty , Potsdam 14469, Germany

4. Broad Institute of MIT and Harvard , Cambridge, Massachusetts 02142, United States

5. Department of Computer Science, University of Manchester , Manchester M13 9PL, United Kingdom

6. Department of Statistics, University of Oxford , Oxford OX1 2JD, United Kingdom

7. Hasso Plattner Institute for Digital Health at Mount Sinai, Icahn School of Medicine at Mount Sinai , New York, New York 10065, United States

Abstract

Abstract Motivation Existing methods for simulating synthetic genotype and phenotype datasets have limited scalability, constraining their usability for large-scale analyses. Moreover, a systematic approach for evaluating synthetic data quality and a benchmark synthetic dataset for developing and evaluating methods for polygenic risk scores are lacking. Results We present HAPNEST, a novel approach for efficiently generating diverse individual-level genotypic and phenotypic data. In comparison to alternative methods, HAPNEST shows faster computational speed and a lower degree of relatedness with reference panels, while generating datasets that preserve key statistical properties of real data. These desirable synthetic data properties enabled us to generate 6.8 million common variants and nine phenotypes with varying degrees of heritability and polygenicity across 1 million individuals. We demonstrate how HAPNEST can facilitate biobank-scale analyses through the comparison of seven methods to generate polygenic risk scoring across multiple ancestry groups and different genetic architectures. Availability and implementation A synthetic dataset of 1 008 000 individuals and nine traits for 6.8 million common variants is available at https://www.ebi.ac.uk/biostudies/studies/S-BSST936. The HAPNEST software for generating synthetic datasets is available as Docker/Singularity containers and open source Julia and C code at https://github.com/intervene-EU-H2020/synthetic_data.

Funder

European Union’s Horizon 2020 research and innovation programme

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Cited by 5 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