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Biology subjects

Ameen, F.

Publications and source records attributed to Ameen, F..

2 recordsLinked to original sources

Kontextual: Reframing analysis of spatial omics data reveals consistent cell relationships across images

State-of-the-art spatial proteomic and transcriptomic technologies can deeply pheno-type cells in their native tissue environment, providing a high throughput means to effectively quantify spatial relationships between diverse cell populations. However, the experimental design choice of which regions of a tissue will be imaged can greatly impact the interpretation of spatial quantifications. That is, spatial relationships identified in one region of interest may not be interpreted consistently across other regions. To address this challenge, we introduce Kontextual, a method which considers alternative frames of reference for contextualising spatial relationships. These contexts may represent landmarks, spatial domains, or groups of functionally similar cells which are consistent across regions. By modelling spatial relationships between cells relative to these contexts, Kontextual produces robust spatial quantifications that are not confounded by the region selected. We demonstrate in spatial proteomics and spatial transcriptomics datasets that modelling spatial relationships this way is biologically meaningful. We also demonstrate how this approach can be used in a classification setting to improve prediction of patient prognosis.

bioinformatics↗

Biologically-informed self-supervised learning for segmentation of subcellular spatial transcriptomics data

Recent advances in subcellular imaging transcriptomics platforms have enabled high-resolution spatial mapping of gene expression, while also introducing significant analytical challenges in accurately identifying cells and assigning transcripts. Existing methods grapple with cell segmentation, frequently leading to fragmented cells or oversized cells that capture contaminated expression. To this end, we present BIDCell, a self-supervised deep learning-based framework with biologically-informed loss functions that learn relationships between spatially resolved gene expression and cell morphology. BIDCell incorporates cell-type data, including single-cell transcriptomics data from public repositories, with cell morphology information. Using a comprehensive evaluation framework consisting of metrics in five complementary categories for cell segmentation performance, we demonstrate that BIDCell outperforms other state-of-the-art methods according to many metrics across a variety of tissue types and technology platforms. Our findings underscore the potential of BIDCell to significantly enhance single-cell spatial expression analyses, including cell-cell interactions, enabling great potential in biological discovery.

bioinformatics↗