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Jaewon Chung

Publications and source records attributed to Jaewon Chung.

6 recordsLinked to original sources

Multiscale Comparative Connectomics

The connectome, a map of the structural and/or functional connections in the brain, provides a complex representation of the neurobiological phenotypes on which it supervenes. This information-rich data modality has the potential to transform our understanding of the relationship between patterns in brain connectivity and neurological processes, disorders, and diseases. However, existing computational techniques used to analyze connectomes are oftentimes insufficient for interrogating multi-subject connectomics datasets: many current methods are either solely designed to analyze single connectomes or leverage heuristic graph statistics that are unable to capture the complete topology of multiscale connections between brain regions. To enable more rigorous connectomics analysis, we introduce a set of robust and interpretable effect size measures motivated by recent theoretical advances in random graph models. These measures facilitate simultaneous analysis of multiple connectomes across different scales of network topology, enabling the robust and reproducible discovery of hierarchical brain structures that vary in relation to phenotypic profiles. In addition to explaining the theoretical foundations and guarantees of our algorithms, we demonstrate their superiority over current state-of-the-art connectomics methods through extensive simulation studies and real-data experiments. Using a set of high-resolution connectomes obtained from genetically distinct mouse strains (including the BTBR mouse -- a standard model of autism -- and three behavioral wild-types), we illustrate how our methods successfully uncover latent information in multi-subject connectomics data and yield valuable insights into the connective correlates of neurological phenotypes that other methods do not capture. The data and code necessary to reproduce our analyses are available at https://github.com/neurodata/MCC.

q-bio.NC

Independence Testing for Temporal Data

Temporal data are increasingly prevalent in modern data science. A fundamental question is whether two time series are related or not. Existing approaches often have limitations, such as relying on parametric assumptions, detecting only linear associations, and requiring multiple tests and corrections. While many non-parametric and universally consistent dependence measures have recently been proposed, directly applying them to temporal data can inflate the p-value and result in an invalid test. To address these challenges, this paper introduces the temporal dependence statistic with block permutation to test independence between temporal data. Under proper assumptions, the proposed procedure is asymptotically valid and universally consistent for testing independence between stationary time series, and capable of estimating the optimal dependence lag that maximizes the dependence. Moreover, it is compatible with a rich family of distance and kernel based dependence measures, eliminates the need for multiple testing, and exhibits excellent testing power in various simulation settings.

stat.ML

Learning sources of variability from high-dimensional observational studies

Causal inference studies whether the presence of a variable influences an observed outcome. As measured by quantities such as the "average treatment effect," this paradigm is employed across numerous biological fields, from vaccine and drug development to policy interventions. Unfortunately, the majority of these methods are often limited to univariate outcomes. Our work generalizes causal estimands to outcomes with any number of dimensions or any measurable space, and formulates traditional causal estimands for nominal variables as causal discrepancy tests. We propose a simple technique for adjusting universally consistent conditional independence tests and prove that these tests are universally consistent causal discrepancy tests. Numerical experiments illustrate that our method, Causal CDcorr, leads to improvements in both finite sample validity and power when compared to existing strategies. Our methods are all open source and available at github.com/ebridge2/cdcorr.

stat.ME

Valid Two-Sample Graph Testing via Optimal Transport Procrustes and Multiscale Graph Correlation with Applications in Connectomics

Testing whether two graphs come from the same distribution is of interest in many real world scenarios, including brain network analysis. Under the random dot product graph model, the nonparametric hypothesis testing frame-work consists of embedding the graphs using the adjacency spectral embedding (ASE), followed by aligning the embeddings using the median flip heuristic, and finally applying the nonparametric maximum mean discrepancy(MMD) test to obtain a p-value. Using synthetic data generated from Drosophila brain networks, we show that the median flip heuristic results in an invalid test, and demonstrate that optimal transport Procrustes (OTP) for alignment resolves the invalidity. We further demonstrate that substituting the MMD test with multiscale graph correlation(MGC) test leads to a more powerful test both in synthetic and in simulated data. Lastly, we apply this powerful test to the right and left hemispheres of the larval Drosophila mushroom body brain networks, and conclude that there is not sufficient evidence to reject the null hypothesis that the two hemispheres are equally distributed.

stat.ME

Sparse Projection Oblique Randomer Forests

Decision forests, including Random Forests and Gradient Boosting Trees, have recently demonstrated state-of-the-art performance in a variety of machine learning settings. Decision forests are typically ensembles of axis-aligned decision trees; that is, trees that split only along feature dimensions. In contrast, many recent extensions to decision forests are based on axis-oblique splits. Unfortunately, these extensions forfeit one or more of the favorable properties of decision forests based on axis-aligned splits, such as robustness to many noise dimensions, interpretability, or computational efficiency. We introduce yet another decision forest, called "Sparse Projection Oblique Randomer Forests" (SPORF). SPORF uses very sparse random projections, i.e., linear combinations of a small subset of features. SPORF significantly improves accuracy over existing state-of-the-art algorithms on a standard benchmark suite for classification with >100 problems of varying dimension, sample size, and number of classes. To illustrate how SPORF addresses the limitations of both axis-aligned and existing oblique decision forest methods, we conduct extensive simulated experiments. SPORF typically yields improved performance over existing decision forests, while mitigating computational efficiency and scalability and maintaining interpretability. SPORF can easily be incorporated into other ensemble methods such as boosting to obtain potentially similar gains.

stat.ML

GraSPy: Graph Statistics in Python

We introduce GraSPy, a Python library devoted to statistical inference, machine learning, and visualization of random graphs and graph populations. This package provides flexible and easy-to-use algorithms for analyzing and understanding graphs with a scikit-learn compliant API. GraSPy can be downloaded from Python Package Index (PyPi), and is released under the Apache 2.0 open-source license. The documentation and all releases are available at https://neurodata.io/graspy.

cs.SI