FLASH-MM: fast and scalable single-cell differential expression analysis using linear mixed-effects models
Single-cell RNA sequencing (scRNA-seq) enables detailed comparisons of gene expression across cells and conditions. Single-cell differential expression analysis faces challenges like sample correlation, individual variation, and scalability. We develop a fast and scalable linear mixed-effects model (LMM) estimation algorithm, FLASH-MM, to address these issues. We reformulate aspects of the linear mixed model estimation procedure to make it faster, by reducing computational complexity and memory usage. Simulation studies with scRNA-seq data show that FLASH-MM is accurate, computationally efficient, effectively controls false positive rates, and maintains high statistical power in differential expression analysis. Tests on tuberculosis immune and kidney single cell data demonstrate FLASH-MM's utility in accelerating single-cell differential expression analysis across diverse biological contexts.
Authors
- Hamed Heydari (ORCID: https://orcid.org/0000-0001-6708-9116)
- Véronique Voisin (ORCID: https://orcid.org/0000-0002-3405-9532)
- Delaram Pouyabahar (ORCID: https://orcid.org/0000-0002-8686-8067)
- Changjiang Xu
- Gary D. Bader
Institutions
- University Health Network (CA)
- Toronto Public Health (CA)
- University of Toronto (CA)
- Lunenfeld-Tanenbaum Research Institute (CA)
- Princess Margaret Cancer Centre (CA)
Publication Details
- Journal
- Nature Communications
- Published
- 2026-02-05
- DOI
- https://doi.org/10.1038/s41467-026-69063-2
- Primary Topic
- Single-cell and spatial transcriptomics
- Type
- article
- Field-Weighted Citation Impact
- 0.00