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Soelistyo, C. J.

Publications and source records attributed to Soelistyo, C. J..

2 recordsLinked to original sources

Virtual perturbations to assess explainability of deep-learning based cell fate predictors

Explainable deep learning holds significant promise in extracting scientific insights from experimental observations. This is especially so in the field of bio-imaging, where the raw data is often voluminous, yet extremely variable and difficult to study. However, one persistent challenge in deep learning assisted scientific discovery is that the workings of artificial neural networks are often difficult to interpret. Here we present a simple technique for investigating the behaviour of trained neural networks: virtual perturbation. By making precise and systematic alterations to input data or internal representations thereof, we are able to discover causal relationships in the outputs of a deep learning model, and by extension, in the underlying phenomenon itself. As an exemplar, we use our recently described deep-learning based cell fate prediction model. We trained the network to predict the fate of less fit cells in an experimental model of mechanical cell competition. By applying virtual perturbation to the trained network, we discover causal relationships between a cells environment and eventual fate. We compare these with known properties of the biological system under investigation to demonstrate that the model faithfully captures insights previously established by experimental research.

biophysics↗

Learning dynamic image representations for self-supervised cell cycle annotation

Time-based comparisons of single-cell trajectories are challenging due to their intrinsic heterogeneity, autonomous decisions, dynamic transitions and unequal lengths. In this paper, we present a self-supervised framework combining an image autoencoder with dynamic time series analysis of latent feature space to represent, compare and annotate cell cycle phases across singlecell trajectories. In our fully data-driven approach, we map similarities between heterogeneous cell tracks and generate statistical representations of single-cell trajectory phase durations, onset and transitions. This work is a first effort to transform a sequence of learned image representations from cell cycle-specific reporters into an unsupervised sequence annotation.

cell biology↗