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Yordan P. Raykov

Publications and source records attributed to Yordan P. Raykov.

12 recordsLinked to original sources

Shrinkage priors for Bayesian Substitute Confounders

Multi-cause observational studies contain information about unmeasured confounding through the dependence structure among causes. However, literal imputation of the unobserved confounder is often more complex than learning a lower-dimensional substitute score that preserves the shared assignment variation needed for stable causal adjustment. The deconfounder (Wang and Blei, 2019) and related substitute confounder methods exploit this idea, but flexible assignment models can fit the joint distribution of the causes while producing scores that over-encode the treatment vector, collapse overlap, or capture single-cause variation. We develop a Bayesian factor assignment framework for learning sparse substitute confounders that retain coarse multi-cause dependence with shrinkage priors. The theory is stated at the level of posterior concentration, factor score contraction, and overlap-preserving assignment geometry and therefore does not rely on a particular shrinkage prior. Under these conditions, the proposed regression-adjusted estimators are consistent for mean potential outcomes when the corresponding latent variable identification assumptions hold. Shrinkage priors provide a natural tool for latent structural learning: they favour low-dimensional factors supported by multiple causes, discourage effectively single-cause factors, and induce an ordering of the latent factors through progressive shrinkage. Synthetic experiments illustrate the roles of signal strength, outcome validity, and geometry-aware regularization. In an Alzheimer's Disease Neuroimaging Initiative (ADNI) baseline analysis, sparse substitute scores recover much of the adjustment obtained by directly conditioning on invasive cerebrospinal-fluid biomarkers, while collapse diagnostics identify when fitted factors reduce to individual observed measurements.

stat.ME

Kernel-based estimators for functional causal effects

We propose causal effect estimators based on empirical Fr\'{e}chet means and operator-valued kernels, tailored to functional data spaces. These methods address the challenges of high-dimensionality, sequential ordering, and model complexity while preserving robustness to treatment misspecification. Using structural assumptions, we obtain compact representations of potential outcomes, enabling scalable estimation of causal effects over time and across covariates. We provide both theoretical, regarding the consistency of functional causal effects, as well as empirical comparison of a range of proposed causal effect estimators. Applications to binary treatment settings with functional outcomes illustrate the framework's utility in biomedical monitoring, where outcomes exhibit complex temporal dynamics. Our estimators accommodate scenarios with registered covariates and outcomes, aligning them to the Fr\'{e}chet means, as well as cases requiring higher-order representations to capture intricate covariate-outcome interactions. These advancements extend causal inference to dynamic and non-linear domains, offering new tools for understanding complex treatment effects in functional data settings.

stat.ME

Analysis of Evolving Cortical Neuronal Networks Using Visual Informatics

Understanding how neuronal population activity changes during development and after stimulation is essential for studying neuronal network dynamics. This work examines how visual informatics can summarize high-dimensional spiking activity while retaining information that is biologically interpretable. We develop a framework based on Minimum-Distortion Embedding (MDE), and compare it with Principal Component Analysis (PCA) and t-distributed Stochastic Neighbor Embedding (t-SNE). In addition to evaluating the embeddings by visual separation, we quantify whether they preserve the cosine-shape radius within each condition and the pairwise distances between condition centroids. Our \emph{in silico} experiments show that MDE with a cosine metric captures the trajectory of simulated network maturation and preserves the contraction of the activity cloud as connectivity increases. Complementary \emph{in vitro} experiments on human cortical cultures show a coherent developmental trajectory from Day In VITRO 23 (DIV23) to DIV64. We also study weak and strong stimulation in simulation, and long-term potentiation stimulation in primary cortical cultures. In the stimulation experiments, MDE separates activity phases more clearly than PCA and preserves transient changes in within-phase variability that are missed by PCA. These results show that metric selection is central to dimensionality reduction of neuronal data. In particular, cosine distance between population activity vectors provides embeddings that better reflect changes in population activity patterns than Euclidean distance. The proposed framework provides a quantitative way to visualize network development and stimulation-induced changes in neuronal activity.

q-bio.NC

TSDF: A simple yet comprehensive, unified data storage and exchange format standard for digital biosensor data in health applications

Digital sensors are increasingly being used to monitor the change over time of physiological processes in biological health and disease, often using wearable devices. This generates very large amounts of digital sensor data, for which, a consensus on a common storage, exchange and archival data format standard, has yet to be reached. To address this gap, we propose Time Series Data Format (TSDF): a unified, standardized format for storing all types of physiological sensor data, across diverse disease areas. We pose a series of format design criteria and review in detail current storage and exchange formats. When judged against these criteria, we find these current formats lacking, and propose a very simple, intuitive standard for both numerical sensor data and metadata, based on raw binary data and JSON-format text files, for sensor measurements/timestamps and metadata, respectively. By focusing on the common characteristics of diverse biosensor data, we define a set of necessary and sufficient metadata fields for storing, processing, exchanging, archiving and reliably interpreting, multi-channel biological time series data. Our aim is for this standardized format to increase the interpretability and exchangeability of data, thereby contributing to scientific reproducibility in studies where digital biosensor data forms a key evidence base.

cs.DB

Few-shot time series segmentation using prototype-defined infinite hidden Markov models

We propose a robust framework for interpretable, few-shot analysis of non-stationary sequential data based on flexible graphical models to express the structured distribution of sequential events, using prototype radial basis function (RBF) neural network emissions. A motivational link is demonstrated between prototypical neural network architectures for few-shot learning and the proposed RBF network infinite hidden Markov model (RBF-iHMM). We show that RBF networks can be efficiently specified via prototypes allowing us to express complex nonstationary patterns, while hidden Markov models are used to infer principled high-level Markov dynamics. The utility of the framework is demonstrated on biomedical signal processing applications such as automated seizure detection from EEG data where RBF networks achieve state-of-the-art performance using a fraction of the data needed to train long-short-term memory variational autoencoders.

cs.LG

Controlling for sparsity in sparse factor analysis models: adaptive latent feature sharing for piecewise linear dimensionality reduction

Ubiquitous linear Gaussian exploratory tools such as principle component analysis (PCA) and factor analysis (FA) remain widely used as tools for: exploratory analysis, pre-processing, data visualization and related tasks. However, due to their rigid assumptions including crowding of high dimensional data, they have been replaced in many settings by more flexible and still interpretable latent feature models. The Feature allocation is usually modelled using discrete latent variables assumed to follow either parametric Beta-Bernoulli distribution or Bayesian nonparametric prior. In this work we propose a simple and tractable parametric feature allocation model which can address key limitations of current latent feature decomposition techniques. The new framework allows for explicit control over the number of features used to express each point and enables a more flexible set of allocation distributions including feature allocations with different sparsity levels. This approach is used to derive a novel adaptive Factor analysis (aFA), as well as, an adaptive probabilistic principle component analysis (aPPCA) capable of flexible structure discovery and dimensionality reduction in a wide case of scenarios. We derive both standard Gibbs sampler, as well as, an expectation-maximization inference algorithms that converge orders of magnitude faster to a reasonable point estimate solution. The utility of the proposed aPPCA model is demonstrated for standard PCA tasks such as feature learning, data visualization and data whitening. We show that aPPCA and aFA can infer interpretable high level features both when applied on raw MNIST and when applied for interpreting autoencoder features. We also demonstrate an application of the aPPCA to more robust blind source separation for functional magnetic resonance imaging (fMRI).

cs.LG

Probabilistic modelling of gait for robust passive monitoring in daily life

Passive monitoring in daily life may provide invaluable insights about a person's health throughout the day. Wearable sensor devices are likely to play a key role in enabling such monitoring in a non-obtrusive fashion. However, sensor data collected in daily life reflects multiple health and behavior related factors together. This creates the need for structured principled analysis to produce reliable and interpretable predictions that can be used to support clinical diagnosis and treatment. In this work we develop a principled modelling approach for free-living gait (walking) analysis. Gait is a promising target for non-obtrusive monitoring because it is common and indicative of various movement disorders such as Parkinson's disease (PD), yet its analysis has largely been limited to experimentally controlled lab settings. To locate and characterize stationary gait segments in free living using accelerometers, we present an unsupervised statistical framework designed to segment signals into differing gait and non-gait patterns. Our flexible probabilistic framework combines empirical assumptions about gait into a principled graphical model with all of its merits. We demonstrate the approach on a new video-referenced dataset including unscripted daily living activities of 25 PD patients and 25 controls, in and around their own houses. We evaluate our ability to detect gait and predict medication induced fluctuations in PD patients based on modelled gait. Our evaluation includes a comparison between sensors attached at multiple body locations including wrist, ankle, trouser pocket and lower back.

cs.HC

Automatic Quality Control and Enhancement for Voice-Based Remote Parkinson's Disease Detection

The performance of voice-based Parkinson's disease (PD) detection systems degrades when there is an acoustic mismatch between training and operating conditions caused mainly by degradation in test signals. In this paper, we address this mismatch by considering three types of degradation commonly encountered in remote voice analysis, namely background noise, reverberation and nonlinear distortion, and investigate how these degradations influence the performance of a PD detection system. Given that the specific degradation is known, we explore the effectiveness of a variety of enhancement algorithms in compensating this mismatch and improving the PD detection accuracy. Then, we propose two approaches to automatically control the quality of recordings by identifying the presence and type of short-term and long-term degradations and protocol violations in voice signals. Finally, we experiment with using the proposed quality control methods to inform the choice of enhancement algorithm. Experimental results using the voice recordings of the mPower mobile PD data set under different degradation conditions show the effectiveness of the quality control approaches in selecting an appropriate enhancement method and, consequently, in improving the PD detection accuracy. This study is a step towards the development of a remote PD detection system capable of operating in unseen acoustic environments.

eess.AS

Adaptive probabilistic principal component analysis

Using the linear Gaussian latent variable model as a starting point we relax some of the constraints it imposes by deriving a nonparametric latent feature Gaussian variable model. This model introduces additional discrete latent variables to the original structure. The Bayesian nonparametric nature of this new model allows it to adapt complexity as more data is observed and project each data point onto a varying number of subspaces. The linear relationship between the continuous latent and observed variables make the proposed model straightforward to interpret, resembling a locally adaptive probabilistic PCA (A-PPCA). We propose two alternative Gibbs sampling procedures for inference in the new model and demonstrate its applicability on sensor data for passive health monitoring.

stat.ML

Probabilistic modelling of gait for remote passive monitoring applications

Passive and non-obtrusive health monitoring using wearables can potentially bring new insights into the user's health status throughout the day and may support clinical diagnosis and treatment. However, identifying segments of free-living data that sufficiently reflect the user's health is challenging. In this work we have studied the problem of modelling real-life gait which is a very indicative behaviour for multiple movement disorders including Parkinson's disease (PD). We have developed a probabilistic framework for unsupervised analysis of the gait, clustering it into different types, which can be used to evaluate gait abnormalities occurring in daily life. Using a unique dataset which contains sensor and video recordings of people with and without PD in their own living environment, we show that our model driven approach achieves high accuracy gait detection and can capture clinical improvement after medication intake.

eess.SP

A unified algorithm framework for quality control of sensor data for behavioural clinimetric testing

The use of smartphone and wearable sensing technology for objective, non-invasive and remote clinimetric testing of symptoms has considerable potential. However, the clinimetric accuracy achievable with such technology is highly reliant on separating the useful from irrelevant or confounded sensor data. Monitoring patient symptoms using digital sensors outside of controlled, clinical lab settings creates a variety of practical challenges, such as unavoidable and unexpected user behaviours. These behaviours often violate the assumptions of clinimetric testing protocols, where these protocols are designed to probe for specific symptoms. Such violations are frequent outside the lab, and can affect the accuracy of the subsequent data analysis and scientific conclusions. At the same time, curating sensor data by hand after the collection process is inherently subjective, laborious and error-prone. To address these problems, we report on a unified algorithmic framework for automated sensor data quality control, which can identify those parts of the sensor data which are sufficiently reliable for further analysis. Algorithms which are special cases of this framework for different sensor data types (e.g. accelerometer, digital audio) detect the extent to which the sensor data adheres to the assumptions of the test protocol for a variety of clinimetric tests. The approach is general enough to be applied to a large set of clinimetric tests and we demonstrate its performance on walking, balance and voice smartphone-based tests, designed to monitor the symptoms of Parkinson's disease.

eess.SP

Simple approximate MAP Inference for Dirichlet processes

The Dirichlet process mixture (DPM) is a ubiquitous, flexible Bayesian nonparametric statistical model. However, full probabilistic inference in this model is analytically intractable, so that computationally intensive techniques such as Gibb's sampling are required. As a result, DPM-based methods, which have considerable potential, are restricted to applications in which computational resources and time for inference is plentiful. For example, they would not be practical for digital signal processing on embedded hardware, where computational resources are at a serious premium. Here, we develop simplified yet statistically rigorous approximate maximum a-posteriori (MAP) inference algorithms for DPMs. This algorithm is as simple as K-means clustering, performs in experiments as well as Gibb's sampling, while requiring only a fraction of the computational effort. Unlike related small variance asymptotics, our algorithm is non-degenerate and so inherits the "rich get richer" property of the Dirichlet process. It also retains a non-degenerate closed-form likelihood which enables standard tools such as cross-validation to be used. This is a well-posed approximation to the MAP solution of the probabilistic DPM model.

stat.ML