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Ramnarine, T. J. S.

Publications and source records attributed to Ramnarine, T. J. S..

2 recordsLinked to original sources

scDynOmics: An Optimized Transformer Model for Representation Learning from Single-Cell Multiomics

As foundation models have become increasingly prevalent in several fields for multiple purposes, pretraining models with single-cell transcriptomic data has gained significant interest. Although existing single-cell foundation models have demonstrated that transformer-based designs can be applied to various biological tasks, they do not show consistently competitive performance compared to much simpler approaches while requiring much more resources in terms of data and compute. Here, we introduce scDynOmics, a pretrainable multiomics-capable transformer for representation learning from single-cell data. The model is motivated by gene regulatory networks without excluding unknown interactions between genes and adopts a Linformer-style attention mechanism to scale to coding-genome wide multimodal inputs. Pretraining on paired single-cell transcriptomic and chromatin accessibility profiles yields compact high-fidelity embeddings that represent cellular states and developmental dynamics. For versatile application, scDynOmics employs low-rank adaptation modules, enabling parameter-efficient fine-tuning for downstream tasks. We demonstrate that scDynOmics outperforms existing single-cell foundation models by a large margin and achieves or surpasses state-of-the-art performance compared to simpler approaches, while revealing interpretable factors driving developmental trajectories and perturbation responses that simpler approaches cannot provide. Overall, scDynOmics is an efficient, scalable, flexible, and interpretable framework for cellular representation learning and deciphering cellular heterogeneity and dynamics.

bioinformatics↗

Sample-multiplexed FACS-preprocessing of PBMCs enables scalable scRNA-seq without compromising transcriptomic or cellular integrity

Efficient preprocessing of peripheral blood mononuclear cells (PBMCs) for single-cell RNA-Sequencing (scRNA-seq) is crucial to ensure high sample throughput while maintaining sample integrity. In particular, when enrichment of rare immune cell populations is necessary to enable their representative profiling among more common PBMCs, sample preprocessing may become a detrimental bottleneck. Here, we present an optimized fluorescence-activated cell sorting (FACS)-based preprocessing workflow designed to enrich rare immune cells while conserving overall PBMC composition. The protocol integrates dead cell removal, targeted rare cell enrichment, channel splitting, and hash-based sample multiplexing together with a new powerful yet lightweight demultiplexing tool (YAHD), improving throughput and cell yield, reducing batch effects, and preserving biological context. Validation across cryopreserved human PBMCs obtained from different scientifically relevant sources (clinical routine and laboratory setting) demonstrated improved sample viability and representation of rare subsets in the final scRNA-seq data. Thorough transcriptomic assessment confirmed non-concerning levels of stress induction and T cell activation as well as low technical variability, removing concerns around FACS-processing, cross-donor multiplexing and channel splitting. The presented approach enables scalable and biologically faithful PBMC preprocessing for scRNA-seq, advancing the study of immune heterogeneity in health and disease.

genomics↗