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Using Fast Weights to Attend to the Recent Past

Neural Information Processing Systems

Until recently, research on artificial neural networks was largely restricted to systems with only two types of variable: Neural activities that represent the current or recent input and weights that learn to capture regularities among inputs, outputs and payoffs. There is no good reason for this restriction. Synapses have dynamics at many different time-scales and this suggests that artificial neural networks might benefit from variables that change slower than activities but much faster than the standard weights. These "fast weights" can be used to store temporary memories of the recent past and they provide a neurally plausible way of implementing the type of attention to the past that has recently proved very helpful in sequence-to-sequence models. By using fast weights we can avoid the need to store copies of neural activity patterns.


A state-space model of cross-region dynamic connectivity in MEG/EEG

Neural Information Processing Systems

Cross-region dynamic connectivity, which describes the spatio-temporal dependence of neural activity among multiple brain regions of interest (ROIs), can provide important information for understanding cognition. For estimating such connectivity, magnetoencephalography (MEG) and electroencephalography (EEG) are well-suited tools because of their millisecond temporal resolution. However, localizing source activity in the brain requires solving an under-determined linear problem. In typical two-step approaches, researchers first solve the linear problem with generic priors assuming independence across ROIs, and secondly quantify cross-region connectivity. In this work, we propose a one-step state-space model to improve estimation of dynamic connectivity. The model treats the mean activity in individual ROIs as the state variable and describes non-stationary dynamic dependence across ROIs using time-varying auto-regression. Compared with a two-step method, which first obtains the commonly used minimum-norm estimates of source activity, and then fits the auto-regressive model, our state-space model yielded smaller estimation errors on simulated data where the model assumptions held. When applied on empirical MEG data from one participant in a scene-processing experiment, our state-space model also demonstrated intriguing preliminary results, indicating leading and lagged linear dependence between the early visual cortex and a higher-level scene-sensitive region, which could reflect feedforward and feedback information flow within the visual cortex during scene processing.






Distributed Flexible Nonlinear Tensor Factorization

Neural Information Processing Systems

Tensor factorization is a powerful tool to analyse multi-way data. Recently proposed nonlinear factorization methods, although capable of capturing complex relationships, are computationally quite expensive and may suffer a severe learning bias in case of extreme data sparsity. Therefore, we propose a distributed, flexible nonlinear tensor factorization model, which avoids the expensive computations and structural restrictions of the Kronecker-product in the existing TGP formulations, allowing an arbitrary subset of tensorial entries to be selected for training. Meanwhile, we derive a tractable and tight variational evidence lower bound (ELBO) that enables highly decoupled, parallel computations and high-quality inference. Based on the new bound, we develop a distributed, key-value-free inference algorithm in the MAPREDUCE framework, which can fully exploit the memory cache mechanism in fast MAPREDUCE systems such as SPARK. Experiments demonstrate the advantages of our method over several state-of-the-art approaches, in terms of both predictive performance and computational efficiency.


Hypothesis Testing in Unsupervised Domain Adaptation with Applications in Alzheimer's Disease

Neural Information Processing Systems

We only observe their transformed versions h(xis) and g(xit), for some known function class h() and g(). Our goal is to perform a statistical test checking if Psource = Ptarget while removing the distortions induced by the transformations. This problem is closely related to domain adaptation, and in our case, is motivated by the need to combine clinical and imaging based biomarkers from multiple sites and/or batches - a fairly common impediment in conducting analyses with much larger sample sizes. We address this problem using ideas from hypothesis testing on the transformed measurements, wherein the distortions need to be estimated in tandem with the testing. We derive a simple algorithm and study its convergence and consistency properties in detail, and provide lower-bound strategies based on recent work in continuous optimization. On a dataset of individuals at risk for Alzheimer's disease, our framework is competitive with alternative procedures that are twice as expensive and in some cases operationally infeasible to implement.