ArticlebioRxiv : the preprint server for biology2026
scDesignPop generates realistic population-scale single-cell RNA-seq for power analysis, benchmarking, and privacy protection.
Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Single-cell RNA sequencing (scRNA-seq) combined with genotyping in large cohorts has enabled the discovery of genetic associations with molecular traits (e.g., eQTLs) at cell-type resolution. However, generating population-scale data remains cost-prohibitive, selecting appropriate analysis methods lacks consensus, and sharing eQTL results alongside scRNA-seq data raises privacy risks. To address these challenges, we introduce scDesignPop, a flexible statistical simulator for generating realistic population-scale scRNA-seq data with genetic effects. scDesignPop models cell- and individual-level covariates, putative cell-type-specific eQTLs (cts-eQTLs), and either real or synthetic genotypes. We validated scDesignPop using the OneK1K and CLUES cohorts across 4 qualitative and 16 quantitative metrics. Unlike splatPop, the only existing population-scale simulator, scDesignPop better preserves eQTL effects and gene-gene dependencies within cell types, closely recapitulating characteristics of the reference data. Leveraging its generative framework, scDesignPop enables power analysis in cell types under multiple eQTL model specifications to guide experimental design; facilitates benchmarking of single-cell eQTL mapping methods through user-defined ground truths; and mitigates re-identification risk using synthetic data while retaining cts-eQTL effects.
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