SearcharxivSearch

arXiv subjects

Matthew A. Smith

Publications and source records attributed to Matthew A. Smith.

5 recordsLinked to original sources

OMiSO: Adaptive optimization of state-dependent brain stimulation to shape neural population states

The coordinated activity of neural populations underlies myriad brain functions. Manipulating this activity using brain stimulation techniques has great potential for scientific and clinical applications, as it provides a tool to causally influence brain function. The state of the brain affects how neural populations respond to incoming sensory stimuli. Thus, taking into account pre-stimulation neural population activity may be crucial to achieve a desired causal manipulation using stimulation. In this work, we propose Online MicroStimulation Optimization (OMiSO), a brain stimulation framework that leverages brain state information to find stimulation parameters that can drive neural population activity toward specified states. OMiSO includes two key advances: i) it leverages the pre-stimulation brain state to choose optimal stimulation parameters, and ii) it adaptively refines the choice of those parameters by considering newly-observed stimulation responses. We tested OMiSO by applying intracortical electrical microstimulation in a monkey and found that it outperformed competing methods that do not incorporate these advances. Taken together, OMiSO provides greater accuracy in achieving specified activity states, thereby advancing neuromodulation technologies for understanding the brain and for treating brain disorders.

q-bio.NC

Simultaneous Inference in Multiple Matrix-Variate Graphs for High-Dimensional Neural Recordings

We study simultaneous inference for multiple matrix-variate Gaussian graphical models in high-dimensional settings. Such models arise when spatiotemporal data are collected across multiple sample groups or experimental sessions, where each group is characterized by its own graphical structure but shares common sparsity patterns. A central challenge is to conduct valid inference on collections of graph edges while efficiently borrowing strength across groups under both high-dimensionality and temporal dependence. We propose a unified framework that combines joint estimation via group penalized regression with a high-dimensional Gaussian approximation bootstrap to enable global testing of edge subsets of arbitrary size. The proposed procedure accommodates temporally dependent observations and avoids naive pooling across heterogeneous groups. We establish theoretical guarantees for the validity of the simultaneous tests under mild conditions on sample size, dimensionality, and non-stationary autoregressive temporal dependence, and show that the resulting tests are nearly optimal in terms of the testable region boundary. The method relies only on convex optimization and parametric bootstrap, making it computationally tractable. Simulation studies and a neural recording example illustrate the efficacy of the proposed approach.

stat.ME

Cross-Population Amplitude Coupling in High-Dimensional Oscillatory Neural Time Series

Neural oscillations have long been considered important markers of interaction across brain regions, yet identifying coordinated oscillatory activity from high-dimensional multiple-electrode recordings remains challenging. We sought to quantify time-varying covariation of oscillatory amplitudes across two brain regions, during a memory task, based on local field potentials recorded from 96 electrodes in each region. We extended Canonical Correlation Analysis (CCA) to multiple time series through the cross-correlation of latent time series. This, however, introduces a large number of possible lead-lag cross-correlations across the two regions. To manage that high dimensionality we developed rigorous statistical procedures aimed at finding a small number of dominant lead-lag effects. The method correctly identified ground truth structure in realistic simulation-based settings. When we used it to analyze local field potentials recorded from prefrontal cortex and visual area V4 we obtained highly plausible results. The new statistical methodology could also be applied to other slowly-varying high-dimensional time series.

stat.ME

False discovery rate regression: an application to neural synchrony detection in primary visual cortex

Many approaches for multiple testing begin with the assumption that all tests in a given study should be combined into a global false-discovery-rate analysis. But this may be inappropriate for many of today's large-scale screening problems, where auxiliary information about each test is often available, and where a combined analysis can lead to poorly calibrated error rates within different subsets of the experiment. To address this issue, we introduce an approach called false-discovery-rate regression that directly uses this auxiliary information to inform the outcome of each test. The method can be motivated by a two-groups model in which covariates are allowed to influence the local false discovery rate, or equivalently, the posterior probability that a given observation is a signal. This poses many subtle issues at the interface between inference and computation, and we investigate several variations of the overall approach. Simulation evidence suggests that: (1) when covariate effects are present, FDR regression improves power for a fixed false-discovery rate; and (2) when covariate effects are absent, the method is robust, in the sense that it does not lead to inflated error rates. We apply the method to neural recordings from primary visual cortex. The goal is to detect pairs of neurons that exhibit fine-time-scale interactions, in the sense that they fire together more often than expected due to chance. Our method detects roughly 50% more synchronous pairs versus a standard FDR-controlling analysis. The companion R package FDRreg implements all methods described in the paper.

stat.ME

The effect of scale-free topology on the robustness and evolvability of genetic regulatory networks

We investigate how scale-free (SF) and Erdos-Renyi (ER) topologies affect the interplay between evolvability and robustness of model gene regulatory networks with Boolean threshold dynamics. In agreement with Oikonomou and Cluzel (2006) we find that networks with SFin topologies, that is SF topology for incoming nodes and ER topology for outgoing nodes, are significantly more evolvable towards specific oscillatory targets than networks with ER topology for both incoming and outgoing nodes. Similar results are found for networks with SFboth and SFout topologies. The functionality of the SFout topology, which most closely resembles the structure of biological gene networks (Babu et al., 2004), is compared to the ER topology in further detail through an extension to multiple target outputs, with either an oscillatory or a non-oscillatory nature. For multiple oscillatory targets of the same length, the differences between SFout and ER networks are enhanced, but for non-oscillatory targets both types of networks show fairly similar evolvability. We find that SF networks generate oscillations much more easily than ER networks do, and this may explain why SF networks are more evolvable than ER networks are for oscillatory phenotypes. In spite of their greater evolvability, we find that networks with SFout topologies are also more robust to mutations than ER networks. Furthermore, the SFout topologies are more robust to changes in initial conditions (environmental robustness). For both topologies, we find that once a population of networks has reached the target state, further neutral evolution can lead to an increase in both the mutational robustness and the environmental robustness to changes in initial conditions.

q-bio.PE