Within a single sniff, the mammalian olfactory system can decode the identity and concentration of odorants wafted on turbulent plumes of air. Yet, it must do so given access only to the noisy, dimensionally-reduced representation of the odor world provided by olfactory receptor neurons. As a result, the olfactory system must solve a compressed sensing problem, relying on the fact that only a handful of the millions of possible odorants are present in a given scene. Inspired by this principle, past works have proposed normative compressed sensing models for olfactory decoding. However, these models have not captured the unique anatomy and physiology of the olfactory bulb, nor have they shown that sensing can be achieved within the 100-millisecond timescale of a single sniff. Here, we propose a rate-based Poisson compressed sensing circuit model for the olfactory bulb.

Here we briefly consider why introducing a prior over the factor matrix enables automatic relevance determination. These ideas reflect results by Bishop [1] and our experiments in Section 3.1. For simplicity, we will first consider the case of factor analysis where p(X) = Q d,tN(xdt; 0,1).

Subjects watched on average 2.6 Hollywood movies, for

Note that this is the case in the present work sinceT 30 minutes is much larger than the longest timescales learned by bGPFA(τ 2s).

Providing a timely intervention before the onset of a critical event, such as a system failure, is of importance in many industrial settings. Before the onset of the critical event, systems typically exhibit behavioral changes which often manifest as stochastic co-variate observations which may be leveraged to trigger intervention. In this paper, for the first time, we formulate the problem of finding an optimally timed intervention (OTI) policy as minimizing the expected residual time to event, subject to a constraint on the probability of missing the event. Existing machine learning approaches to intervention on critical events focus on predicting event occurrence within a pre-defined window (a classification problem) or predicting time-to-event (a regression problem). Interventions are then triggered by setting model thresholds.

Latent variable models are ubiquitous in the exploratory analysis of neural population recordings, where they allow researchers to summarize the activity of large populations of neurons in lower dimensional'latent' spaces. Existing methods can generally be categorized into (i) Bayesian methods that facilitate flexible incorporation of prior knowledge and uncertainty estimation, but which typically do not scale to large datasets; and (ii) highly parameterized methods without explicit priors that scale better but often struggle in the low-data regime. Here, we bridge this gap by developing a fully Bayesian yet scalable version of Gaussian process factor analysis (bGPFA), which models neural data as arising from a set of inferred latent processes with a prior that encourages smoothness over time. Additionally, bGPFA uses automatic relevance determination to infer the dimensionality of neural activity directly from the training data during optimization. To enable the analysis of continuous recordings without trial structure, we introduce a novel variational inference strategy that scales near-linearly in time and also allows for non-Gaussian noise models appropriate for electrophysiological recordings.

Following an instruction involves distinct sub-processes, such as reading content, reading the instruction, executing it, and producing an answer. We ask where, along the layer stack, instruction following begins, the point where reading gives way to doing. We introduce three simple datasets (Key-Value, Quote Attribution, Letter Selection) and two hop compositions of these tasks. Using activation patching on minimal-contrast prompt pairs, we measure a layer-wise flip rate that indicates when substituting selected residual activations changes the predicted answer. Across models in the Llama family, we observe an inflection point, which we term onset, where interventions that change predictions before this point become largely ineffective afterward. Multi-hop compositions show a similar onset location. These results provide a simple, replicable way to locate where instruction following begins and to compare this location across tasks and model sizes.

Thermocouples are in widespread use in industry, but they are particularly susceptible to calibration drift in harsh environments. Self-validating thermocouples aim to address this issue by using a miniature phase-change cell (fixed-point) in close proximity to the measurement junction (tip) of the thermocouple. The fixed point is a crucible containing an ingot of metal with a known melting temperature. When the process temperature being monitored passes through the melting temperature of the ingot, the thermocouple output exhibits a "plateau" during melting. Since the melting temperature of the ingot is known, the thermocouple can be recalibrated in situ. Identifying the melting plateau to determine the onset of melting is reasonably well established but requires manual intervention involving zooming in on the region around the actual melting temperature, a process which can depend on the shape of the melting plateau. For the first time, we present a novel machine learning approach to recognize and identify the characteristic shape of the melting plateau and once identified, to quantity the point at which melting begins, along with its associated uncertainty. This removes the need for human intervention in locating and characterizing the melting point. Results from test data provided by CCPI Europe show 100% accuracy of melting plateau detection. They also show a cross-validated R2 of 0.99 on predictions of calibration drift.

In this study, we present a deep learning framework that learns complex spatio-temporal correlation structures of EEG signals through a Spatio-Temporal Attention Network (ST AN) for accurate predictions of onset of seizures for Epilepsy patients. Unlike existing methods, which rely on feature engineering and/or assume fixed preictal durations, our approach simultaneously models spatio-temporal correlations through ST AN and employs an adversarial discriminator to distinguish preictal from interictal attention patterns, enabling patient-specific learning. Evaluation on CHB-MIT and MSSM datasets demonstrates 96.6% sensitivity with 0.011/h false detection rate on CHB-MIT, and 94.2% sensitivity with 0.063/h FDR on MSSM, significantly outperforming state-of-the-art methods.