Kieran Campbell

MohammadReza Ebrahimi, Navona Calarco, Kieran Campbell et al.

Multi-subject fMRI studies are challenging due to the high variability of both brain anatomy and functional brain topographies across participants. An effective way of aggregating multi-subject fMRI data is to extract a shared representation that filters out unwanted variability among subjects. Some recent work has implemented probabilistic models to extract a shared representation in task fMRI. In the present work, we improve upon these models by incorporating temporal information in the common latent structures. We introduce a new model, Shared Gaussian Process Factor Analysis (S-GPFA), that discovers shared latent trajectories and subject-specific functional topographies, while modelling temporal correlation in fMRI data. We demonstrate the efficacy of our model in revealing ground truth latent structures using simulated data, and replicate experimental performance of time-segment matching and inter-subject similarity on the publicly available Raider and Sherlock datasets. We further test the utility of our model by analyzing its learned model parameters in the large multi-site SPINS dataset, on a social cognition task from participants with and without schizophrenia.

Sana Tonekaboni, Shalmali Joshi, Kieran Campbell et al.

Explanations of time series models are useful for high stakes applications like healthcare but have received little attention in machine learning literature. We propose FIT, a framework that evaluates the importance of observations for a multivariate time-series black-box model by quantifying the shift in the predictive distribution over time. FIT defines the importance of an observation based on its contribution to the distributional shift under a KL-divergence that contrasts the predictive distribution against a counterfactual where the rest of the features are unobserved. We also demonstrate the need to control for time-dependent distribution shifts. We compare with state-of-the-art baselines on simulated and real-world clinical data and demonstrate that our approach is superior in identifying important time points and observations throughout the time series.