Adjusting for Confounding in Unsupervised Latent Representations of Images

Biological imaging data are often partially confounded or contain unwanted variability. Examples of such phenomena include variable lighting across microscopy image captures, stain intensity variation in histological slides, and batch effects for high throughput drug screening assays. Therefore, to develop "fair" models which generalise well to unseen examples, it is crucial to learn data representations that are insensitive to nuisance factors of variation. In this paper, we present a strategy based on adversarial training, capable of learning unsupervised representations invariant to confounders. As an empirical validation of our method, we use deep convolutional autoencoders to learn unbiased cellular representations from microscopy imaging.

Towards Deep Cellular Phenotyping in Placental Histology

The placenta is a complex organ, playing multiple roles during fetal development. Very little is known about the association between placental morphological abnormalities and fetal physiology. In this work, we present an open sourced, computationally tractable deep learning pipeline to analyse placenta histology at the level of the cell. By utilising two deep Convolutional Neural Network architectures and transfer learning, we can robustly localise and classify placental cells within five classes with an accuracy of 89%. Furthermore, we learn deep embeddings encoding phenotypic knowledge that is capable of both stratifying five distinct cell populations and learn intraclass phenotypic variance. We envisage that the automation of this pipeline to population scale studies of placenta histology has the potential to improve our understanding of basic cellular placental biology and its variations, particularly its role in predicting adverse birth outcomes.