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Biology subjects

Lo, M. C. K.

Publications and source records attributed to Lo, M. C. K..

3 recordsLinked to original sources

Generalizable Morphological Profiling of Cells by Interpretable Unsupervised Learning

The intersection of advanced microscopy and machine learning is revolutionizing cell biology into a quantitative, data-driven science. While traditional morphological profiling of cells relies on labor-intensive manual feature extraction susceptible to biases, deep learning offers promising alternatives but struggles with the interpretability of its black-box operation and dependency on extensive labeled data. We introduce MorphoGenie, an unsupervised deep-learning framework designed to address these challenges in single-cell morphological profiling. Enabling disentangled representation learning integrated with high-fidelity image reconstructions, MorphoGenie possesses a critical attribute to learn a compact, generalizable and interpretable latent space. This facilitates the extraction of biologically meaningful features without human annotation, additionally overcoming the "curse of dimensionality" inherent in manual methods. Unlike prior models, MorphoGenie introduces a systematic approach to mapping disentangled latent representations to fundamental hierarchical morphological attributes, ensuring both semantic and biological interpretability. Moreover, it adheres to the concept of combinatorial generalization--a core principle of human intelligence-- which greatly enhances the models capacity to generalize across a broad spectrum of imaging modalities (e.g., quantitative phase imaging and fluorescence imaging) and experimental conditions (ranging from discrete cell type/state classification to continuous trajectory inference). The framework offers a new, generalized strategy for unbiased and comprehensive morphological profiling, potentially revealing insights into cellular behavior in health and disease that might be overlooked by expert visual examination.

bioinformatics↗

Information-Distilled Generative Label-Free Morphological Profiling Encodes Cellular Heterogeneity

Image-based cytometry faces constant challenges due to technical variations arising from different experimental batches and conditions, such as differences in instrument configurations or image acquisition protocols, impeding genuine biological interpretation of cell morphology. Existing solutions, often necessitating extensive pre-existing data knowledge or control samples across batches, have proved limited, especially with complex cell image data. To overcome this, we introduce Cyto-Morphology Adversarial Distillation (CytoMAD), a self-supervised multi-task learning strategy that distills biologically relevant cellular morphological information from batch variations, enabling integrated analysis across multiple data batches without complex data assumptions or extensive manual annotation. Unique to CytoMAD is its "morphology distillation", symbiotically paired with deep-learning image-contrast translation - offering additional interpretable insights into the label-free morphological profiles. We demonstrate the versatile efficacy of CytoMAD in augmenting the power of biophysical imaging cytometry. It allows integrated label-free classification of different human lung cancer cell types and accurately recapitulates their progressive drug responses, even when trained without the drug concentration information. We also applied CytoMAD to jointly analyze tumor biopsies across different non-small-cell lung cancer patients and reveal previously unexplored biophysical cellular heterogeneity, linked to epithelial-mesenchymal plasticity, that standard fluorescence markers overlook. CytoMAD holds promises to substantiate the wide adoption of biophysical cytometry for cost-effective diagnostic and screening applications.

bioengineering↗

starmapVR: immersive visualisation of single cell spatial omic data

MotivationAdvances in high throughput single-cell and spatial omic technologies have enabled the profiling of molecular expression and phenotypic properties of hundreds of thousands of individual cells in the context of their two dimensional (2D) or three dimensional (3D) spatial endogenous arrangement. However, current visualisation techniques do not allow for effective display and exploration of the single cell data in their spatial context. With the widespread availability of low-cost virtual reality (VR) gadgets, such as Google Cardboard, we propose that an immersive visualisation strategy is useful. ResultsWe present starmapVR, a light-weight, cross-platform, web-based tool for visualising single-cell and spatial omic data. starmapVR supports a number of interaction methods, such as keyboard, mouse, wireless controller and voice control. The tool visualises single cells in a 3D space and each cell can be represented by a star plot (for molecular expression, phenotypic properties) or image (for single cell imaging). For spatial transcriptomic data, the 2D single cell expression data can be visualised alongside the histological image in a 2.5D format. The application of starmapVR is demonstrated through a series of case studies. Its scalability has been carefully evaluated across different platforms. Availability and implementationstarmapVR is freely accessible at https://holab-hku.github.io/starmapVR, with the corresponding source code available at https://github.com/holab-hku/starmapVR under the open source MIT license. Supplementary InformationSupplementary data are available at Bioinformatics online.

bioinformatics↗