Alan R. Lowe

Marjan Famili, Jola Mirecka, Camila Rangel Smith et al.

Learning compact and interpretable representations of data is a critical challenge in scientific image analysis. Here, we introduce Affinity-VAE, a generative model that enables us to impose our scientific intuition about the similarity of instances in the dataset on the learned representation during training. We demonstrate the utility of the approach in the scientific domain of cryo-electron tomography (cryo-ET) where a significant current challenge is to identify similar molecules within a noisy and low contrast tomographic image volume. This task is distinct from classification in that, at inference time, it is unknown whether an instance is part of the training set or not. We trained affinity-VAE using prior knowledge of protein structure to inform the latent space. Our model is able to create rotationally-invariant, morphologically homogeneous clusters in the latent representation, with improved cluster separation compared to other approaches. It achieves competitive performance on protein classification with the added benefit of disentangling object pose, structural similarity and an interpretable latent representation. In the context of cryo-ET data, affinity-VAE captures the orientation of identified proteins in 3D which can be used as a prior for subsequent scientific experiments. Extracting physical principles from a trained network is of significant importance in scientific imaging where a ground truth training set is not always feasible.

Christopher J. Soelistyo, Alan R. Lowe

How can we find interpretable, domain-appropriate models of natural phenomena given some complex, raw data such as images? Can we use such models to derive scientific insight from the data? In this paper, we propose some methods for achieving this. In particular, we implement disentangled representation learning, sparse deep neural network training and symbolic regression, and assess their usefulness in forming interpretable models of complex image data. We demonstrate their relevance to the field of bioimaging using a well-studied test problem of classifying cell states in microscopy data. We find that such methods can produce highly parsimonious models that achieve $\sim98\%$ of the accuracy of black-box benchmark models, with a tiny fraction of the complexity. We explore the utility of such interpretable models in producing scientific explanations of the underlying biological phenomenon.