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Peters, D. J. M.

Publications and source records attributed to Peters, D. J. M..

2 recordsLinked to original sources

Integrative learning of disentangled representations from single-cell RNA-sequencing datasets

AO_SCPLOWBSTRACTC_SCPLOWSingle-cell RNA-sequencing is instrumental in studying cellular diversity in biological systems. Using batch correction methods, cell identities are often jointly defined across multiple conditions, individuals, or modalities. These approaches overlook group-specific information and require either paired data or matching features across datasets. Here we present shared-private Variational Inference via Product of Experts with Supervision (spVIPES), a framework to analyze the shared and private components of unpaired groups of cells with non-matching features. spVIPES represents the cells from the different groups as a composite of private and shared factors of variation using a probabilistic latent variable model. We evaluate the performance of spVIPES with a simulated dataset and apply our model in three different scenarios: (i) cross-species comparisons, (ii) regeneration following long and short acute kidney injury, and (iii) IFN-{beta} stimulation of PMBCs. In our study, we demonstrate that spVIPES accurately disentangles distinct sources of variation into private and shared representations while matching current state-of-the-art methods for batch correction. Furthermore, spVIPES shared space outperforms alternatives models at learning cell identities across datasets with non-matching features. We implemented spVIPES using the scvi-tools framework and release it as an open-source software at https://github.com/nrclaudio/spVIPES.

bioinformatics↗

A comprehensive mouse kidney atlas enables rare cell population characterization and robust marker discovery

The cellular diversity and complexity of the kidney are on par with its physiological intricacy. Although our anatomical understanding of the different segments and their functions is supported by a plethora of research, the identification of distinct and rare cell populations and their markers remains elusive. Here, we leverage the large number of cells and nuclei profiles using single-cell (scRNA-seq) and single-nuclei (snRNA-seq) RNA-sequencing to build a comprehensive atlas of the adult mouse kidney. We created MKA (Mouse Kidney Atlas) by integrating 59 publicly available single-cell and single-nuclei transcriptomic datasets from eight independent studies. The atlas contains more than 140.000 cells and nuclei covering different single-cell technologies, age, and tissue sections. To harmonize annotations across datasets, we constructed a hierarchical model of the cell populations present in our atlas. Using this hierarchy, we trained a model to automatically identify cells in unannotated datasets and evaluated its performance against well-established methods and annotation references. Our learnt model is dynamic, allowing the incorporation of novel cell populations and refinement of known profiles as more datasets become available. Using MKA and the learned model of cellular hierarchies, we predicted previously missing cell annotations from several studies and characterized well-studied and rare cell populations. This allowed us to identify reproducible markers across studies for poorly understood cell types and transitional states.

bioinformatics↗