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Research PaperResearchia:202610.28021

HELICS: Biobank-scale Conditional Synthetic Genome Generation via Latent Flow Matching

Ahmad Abdel-Azim

Abstract

Individual-level genotype data underpin genetic discovery, disease-risk modeling, and therapeutic development, yet many critical settings remain data-limited, including underrepresented ancestries, rare or imbalanced disease cohorts, and restricted-access biobanks. Conditional synthetic genome generation would support privacy-aware benchmarking, simulation, and data augmentation, but requires learning an ultra-high-dimensional discrete distribution over hundreds of thousands to tens of millions ...

Submitted: October 28, 2026Subjects: Biology; Biotechnology

Description / Details

Individual-level genotype data underpin genetic discovery, disease-risk modeling, and therapeutic development, yet many critical settings remain data-limited, including underrepresented ancestries, rare or imbalanced disease cohorts, and restricted-access biobanks. Conditional synthetic genome generation would support privacy-aware benchmarking, simulation, and data augmentation, but requires learning an ultra-high-dimensional discrete distribution over hundreds of thousands to tens of millions of correlated single-nucleotide polymorphisms (SNPs), or sites of DNA variation. We introduce HELICS: High-fidelity gEneration via Latent Interpolant Conditional Synthesis, a phasing-free latent flow matching framework for genome-wide SNP-level generation from biobank-scale genotype data. HELICS tokenizes chromosomes with convolutional autoencoders, reducing >600K SNPs to 4,096 continuous latent tokens, and trains a transformer parameterized conditional flow matching model over the concatenated multi-chromosome latent representation. Trained on over 417K genomes in the UK Biobank, HELICS generates genome-wide common-variant synthetic cohorts without haplotype phasing and achieves stronger fidelity to real genotypes than existing haplotype-based simulators, including high allele-frequency agreement in external evaluation and superior preservation of local and long-range SNP correlation structure. Conditioning on ancestry and genetic liability summaries enables targeted generation across genetic risk profiles; in perturbation analyses, by increasing the conditioned disease trait liability, HELICS induces SNP-level dosage changes in generated genomes that are highly correlated with published association weights. HELICS provides a scalable generative modeling framework for SNP-level genome data and a path toward conditional synthetic cohorts for data-limited genetic studies.


Source: arXiv:2610.36361v1 - http://arxiv.org/abs/2610.36361v1 PDF: https://arxiv.org/pdf/2610.36361v1 Original Link: http://arxiv.org/abs/2610.36361v1

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Submission Info
Date:
Oct 28, 2026
Topic:
Biotechnology
Area:
Biology
Comments:
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