SNP2Vec: Scalable Self-Supervised Pre-Training for Genome-Wide Association Study

Samuel Cahyawijaya, Tiezheng Yu, Zihan Liu, Tiffany Mak, Xiaopu Zhou, N. Ip, Pascale Fung
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引用次数: 3

Abstract

Self-supervised pre-training methods have brought remarkable breakthroughs in the understanding of text, image, and speech. Recent developments in genomics has also adopted these pre-training methods for genome understanding. However, they focus only on understanding haploid sequences, which hinders their applicability towards understanding genetic variations, also known as single nucleotide polymorphisms (SNPs), which is crucial for genome-wide association study. In this paper, we introduce SNP2Vec, a scalable self-supervised pre-training approach for understanding SNP. We apply SNP2Vec to perform long-sequence genomics modeling, and we evaluate the effectiveness of our approach on predicting Alzheimer’s disease risk in a Chinese cohort. Our approach significantly outperforms existing polygenic risk score methods and all other baselines, including the model that is trained entirely with haploid sequences.
SNP2Vec:全基因组关联研究的可扩展自监督预训练
自监督预训练方法在文本、图像和语音的理解方面带来了显著的突破。基因组学的最新发展也采用了这些预训练方法来理解基因组。然而,他们只关注于理解单倍体序列,这阻碍了他们对遗传变异的理解,也被称为单核苷酸多态性(snp),这对全基因组关联研究至关重要。在本文中,我们介绍了SNP2Vec,一种可扩展的自监督预训练方法,用于理解SNP。我们应用SNP2Vec进行长序列基因组学建模,并评估我们的方法在预测中国队列阿尔茨海默病风险方面的有效性。我们的方法明显优于现有的多基因风险评分方法和所有其他基线,包括完全用单倍体序列训练的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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