This framework employs Fast Fourier Transform for dimensionality reduction in single-cell RNA sequencing, suggesting enhanced visualization capabilities.
Abstract Single-cell RNA sequencing (scRNA-seq) enables high-resolution profiling of cellular heterogeneity, yet its high dimensionality and sparsity remain major challenges for downstream analysis and visualization. This study introduces a framework that applies the Fast Fourier Transform (FFT) to scRNA-seq expression profiles, converting gene-level signals into frequency-domain representations. By selectively retaining low-frequency components, the method reduces dimensionality while preserving biologically meaningful structure and suppressing technical noise. The approach facilitates clustering, visualization, and annotation tasks. Applied to the PBMC10k dataset, FFT-based compression achieved performance comparable to conventional methods while offering modularity, transparency, and computational efficiency. This framework provides an interpretable and biologically grounded preprocessing strategy for scalable single-cell analysis across transcriptomic and other omics modalities
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Solomon Tessega (2025) studied this question.
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