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Elmalam, N.

Publications and source records attributed to Elmalam, N..

2 recordsLinked to original sources

Trustworthy in silico labeling via semantic visual interpretability of image-to-image translation

Cross-modality image translation promises to provide multiple layers of biological information from a single image input, yet its practical application is stalled by a lack of interpretability and the inability to account for model imperfections. In silico labeling, the inference of organelle localization from label-free images, is a primary example where this black-box nature limits adoption. We present Mask Interpreter, a generalized method for semantic visual interpretability of image-to-image translation models. By uncovering organelle-specific "explanation signatures", Mask Interpreter validates that models rely on authentic biological structures rather than spurious artifacts. Beyond biological validation, it outperforms traditional explainable AI (xAI) approaches, identifies batch effects and localizes prediction errors when ground-truth fluorescence is unavailable. Semantic confidence modeling further provides fine-grained reliability assessment at single-cell resolution, enabling the automated exclusion of artifacts from downstream analyses. By bridging the gap between computational inference and meaningful biological features, Mask Interpreter transforms in silico labeling into a reliable tool for scientific discovery across diverse biomedical imaging modalities.

cell biology↗

Cell-context dependent in silico organelle localization in label-free microscopy images

In silico labeling prediction of organelle fluorescence from label-free microscopy images has the potential to revolutionize our understanding of cells as integrated complex systems. However, out-of-distribution data caused by changes in the intracellular organization across cell types, cellular processes or perturbations, can lead to altered label-free images and impaired in silico labeling. We demonstrated that incorporating biological meaningful cell contexts, via a context-dependent model that we call CELTIC, enhanced in silico labeling prediction and enabled downstream analysis of out-of-distribution data such as cells undergoing mitosis, and cells located at the edge of the colony. These results suggest a link between cell context and intracellular organization. Using CELTIC to generate single cell images transitioning between different contexts enabled us to overcome inter-cell variability toward integrated characterization of organelles alterations in cellular organization. The explicit inclusion of context has the potential to harmonize multiple datasets, paving the way for generalized in silico labeling foundation models.

cell biology↗