GenoBERT: A Language Model for Accurate Genotype Imputation

Fuente: arXiv
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Autores principales: Huang, Lei, Qiu, Chuan, Su, Kuan-Jui, Liu, Anqi, Gong, Yun, Lin, Weiqiang, Jiang, Lindong, Zhao, Chen, Song, Meng, Deng, Jeffrey, Tian, Qing, Luo, Zhe, Gong, Ping, Shen, Hui, Zhang, Chaoyang, Deng, Hong-Wen
Formato: Preprint
Publicado: 2026
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author Huang, Lei
Qiu, Chuan
Su, Kuan-Jui
Liu, Anqi
Gong, Yun
Lin, Weiqiang
Jiang, Lindong
Zhao, Chen
Song, Meng
Deng, Jeffrey
Tian, Qing
Luo, Zhe
Gong, Ping
Shen, Hui
Zhang, Chaoyang
Deng, Hong-Wen
author_facet Huang, Lei
Qiu, Chuan
Su, Kuan-Jui
Liu, Anqi
Gong, Yun
Lin, Weiqiang
Jiang, Lindong
Zhao, Chen
Song, Meng
Deng, Jeffrey
Tian, Qing
Luo, Zhe
Gong, Ping
Shen, Hui
Zhang, Chaoyang
Deng, Hong-Wen
contents Genotype imputation enables dense variant coverage for genome-wide association and risk-prediction studies, yet conventional reference-panel methods remain limited by ancestry bias and reduced rare-variant accuracy. We present Genotype Bidirectional Encoder Representations from Transformers (GenoBERT), a transformer-based, reference-free framework that tokenizes phased genotypes and uses a self-attention mechanism to capture both short- and long-range linkage disequilibrium (LD) dependencies. Benchmarking on two independent datasets including the Louisiana Osteoporosis Study (LOS) and the 1000 Genomes Project (1KGP) across ancestry groups and multiple genotype missingness levels (5-50%) shows that GenoBERT achieves the highest overall accuracy compared to four baseline methods (Beagle5.4, SCDA, BiU-Net, and STICI). At practical sparsity levels (up to 25% missing), GenoBERT attains high overall imputation accuracy ($r^2 approx 0.98$) across datasets, and maintains robust performance ($r^2 > 0.90$) even at 50% missingness. Experimental results across different ancestries confirm consistent gains across datasets, with resilience to small sample sizes and weak LD. A 128-SNP (single-nucleotide polymorphism) context window (approximately 100 Kb) is validated through LD-decay analyses as sufficient to capture local correlation structures. By eliminating reference-panel dependence while preserving high accuracy, GenoBERT provides a scalable and robust solution for genotype imputation and a foundation for downstream genomic modeling.
format Preprint
id arxiv_https___arxiv_org_abs_2604_00058
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle GenoBERT: A Language Model for Accurate Genotype Imputation
Huang, Lei
Qiu, Chuan
Su, Kuan-Jui
Liu, Anqi
Gong, Yun
Lin, Weiqiang
Jiang, Lindong
Zhao, Chen
Song, Meng
Deng, Jeffrey
Tian, Qing
Luo, Zhe
Gong, Ping
Shen, Hui
Zhang, Chaoyang
Deng, Hong-Wen
Genomics
Artificial Intelligence
Machine Learning
Genotype imputation enables dense variant coverage for genome-wide association and risk-prediction studies, yet conventional reference-panel methods remain limited by ancestry bias and reduced rare-variant accuracy. We present Genotype Bidirectional Encoder Representations from Transformers (GenoBERT), a transformer-based, reference-free framework that tokenizes phased genotypes and uses a self-attention mechanism to capture both short- and long-range linkage disequilibrium (LD) dependencies. Benchmarking on two independent datasets including the Louisiana Osteoporosis Study (LOS) and the 1000 Genomes Project (1KGP) across ancestry groups and multiple genotype missingness levels (5-50%) shows that GenoBERT achieves the highest overall accuracy compared to four baseline methods (Beagle5.4, SCDA, BiU-Net, and STICI). At practical sparsity levels (up to 25% missing), GenoBERT attains high overall imputation accuracy ($r^2 approx 0.98$) across datasets, and maintains robust performance ($r^2 > 0.90$) even at 50% missingness. Experimental results across different ancestries confirm consistent gains across datasets, with resilience to small sample sizes and weak LD. A 128-SNP (single-nucleotide polymorphism) context window (approximately 100 Kb) is validated through LD-decay analyses as sufficient to capture local correlation structures. By eliminating reference-panel dependence while preserving high accuracy, GenoBERT provides a scalable and robust solution for genotype imputation and a foundation for downstream genomic modeling.
title GenoBERT: A Language Model for Accurate Genotype Imputation
topic Genomics
Artificial Intelligence
Machine Learning
url https://arxiv.org/abs/2604.00058