scMix: learning temporal dynamics of gene expression under irregular time intervals.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41692970.
- Also identified by DOI 10.1093/bioinformatics/btag080 and PMC identifier 12970592.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Understanding temporal gene expression is fundamental in the study of cellular development and differentiation. In practice, temporal single-cell datasets tend to contain only a limited number of measured time points, which are often unevenly spaced, resulting in irregular intervals between observations due to experimental constraints. Existing methods typically address these intervals by sequentially predicting one time point after another, yet lack mechanisms to explicitly model time intervals, leading to error accumulation. In this work, we introduce scMix, a language-model-based framework for predicting single-cell gene expression, which enables prediction from multiple historical time points. We build scMix on the Receptance Weighted Key Value architecture and use its time decay mechanism to model temporal dependencies over time. Moreover, scMix proposes a delta-time mechanism that allows the model to bypass unmeasured time points, reducing error accumulation and improving robustness. In addition, we incorporate a trend regularization strategy to enhance the temporal coherence of predicted gene expression trajectories. scMix demonstrates state-of-the-art performance in predicting gene expression at unmeasured time points, surpassing existing methods, and also achieves outstanding results on downstream tasks. The code used for this study is available at https://doi.org/10.5281/zenodo.18287184.
Medical subject headings
- Single-Cell Analysis
- Software
- Gene Expression Profiling
- Computational Biology
- Gene Expression