SearcharxivSearch

arXiv subjects

Nicholas J. Tustison

Publications and source records attributed to Nicholas J. Tustison.

4 recordsLinked to original sources

Non-Negative Stiefel Approximating Flow: Orthogonalish Matrix Optimization for Interpretable Embeddings

Interpretable representation learning is a central challenge in modern machine learning, particularly in high-dimensional settings such as neuroimaging, genomics, and text analysis. Current methods often struggle to balance the competing demands of interpretability and model flexibility, limiting their effectiveness in extracting meaningful insights from complex data. We introduce Non-negative Stiefel Approximating Flow (NSA-Flow), a general-purpose matrix estimation framework that unifies ideas from sparse matrix factorization, orthogonalization, and constrained manifold learning. NSA-Flow enforces structured sparsity through a continuous balance between reconstruction fidelity and column-wise decorrelation, parameterized by a single tunable weight. The method operates as a smooth flow near the Stiefel manifold with proximal updates for non-negativity and adaptive gradient control, yielding representations that are simultaneously sparse, stable, and interpretable. Unlike classical regularization schemes, NSA-Flow provides an intuitive geometric mechanism for manipulating sparsity at the level of global structure while simplifying latent features. We demonstrate that the NSA-Flow objective can be optimized smoothly and integrates seamlessly with existing pipelines for dimensionality reduction while improving interpretability and generalization in both simulated and real biomedical data. Empirical validation on the Golub leukemia dataset and in Alzheimer's disease demonstrate that the NSA-Flow constraints can maintain or improve performance over related methods with little additional methodological effort. NSA-Flow offers a scalable, general-purpose tool for interpretable ML, applicable across data science domains.

stat.ML

The Brain Tumor Sequence Registration (BraTS-Reg) Challenge: Establishing Correspondence Between Pre-Operative and Follow-up MRI Scans of Diffuse Glioma Patients

Registration of longitudinal brain MRI scans containing pathologies is challenging due to dramatic changes in tissue appearance. Although there has been progress in developing general-purpose medical image registration techniques, they have not yet attained the requisite precision and reliability for this task, highlighting its inherent complexity. Here we describe the Brain Tumor Sequence Registration (BraTS-Reg) challenge, as the first public benchmark environment for deformable registration algorithms focusing on estimating correspondences between pre-operative and follow-up scans of the same patient diagnosed with a diffuse brain glioma. The BraTS-Reg data comprise de-identified multi-institutional multi-parametric MRI (mpMRI) scans, curated for size and resolution according to a canonical anatomical template, and divided into training, validation, and testing sets. Clinical experts annotated ground truth (GT) landmark points of anatomical locations distinct across the temporal domain. Quantitative evaluation and ranking were based on the Median Euclidean Error (MEE), Robustness, and the determinant of the Jacobian of the displacement field. The top-ranked methodologies yielded similar performance across all evaluation metrics and shared several methodological commonalities, including pre-alignment, deep neural networks, inverse consistency analysis, and test-time instance optimization per-case basis as a post-processing step. The top-ranked method attained the MEE at or below that of the inter-rater variability for approximately 60% of the evaluated landmarks, underscoring the scope for further accuracy and robustness improvements, especially relative to human experts. The aim of BraTS-Reg is to continue to serve as an active resource for research, with the data and online evaluation tools accessible at https://bratsreg.github.io/.

eess.IV

Synthesizing longitudinal cortical thickness estimates with a flexible and hierarchical multivariate measurement-error model

MRI-based entorhinal cortical thickness (eCT) measurements predict cognitive decline in Alzheimer's disease (AD) with low cost and minimal invasiveness. Two prominent imaging paradigms, FreeSurfer (FS) and Advanced Normalization Tools (ANTs), feature multiple pipelines for extracting region-specific eCT measurements from raw MRI, but the sheer complexity of these pipelines makes it difficult to choose between pipelines, compare results between pipelines, and characterize uncertainty in pipeline estimates. Worse yet, the EC is particularly difficult to image, leading to variations in thickness estimates between pipelines that overwhelm physiologicl variations predictive of AD. We examine the eCT outputs of seven different pipelines on MRIs from the Alzheimer's Disease Neuroimaging Initiative. Because of both theoretical and practical limitations, we have no gold standard by which to evaluate them. Instead, we use a Bayesian hierarchical model to combine the estimates. The resulting posterior distribution yields high-probability idealized eCT values that account for inherent uncertainty through a flexible multivariate error model that supports different constant offsets, standard deviations, tailedness, and correlation structures between pipelines. Our hierarchical model directly relates idealized eCTs to clinical outcomes in a way that propagates eCT estimation uncertainty to clinical estimates while accounting for longitudinal structure in the data. Surprisingly, even though it incorporates greater uncertainty in the predictor and regularization provided by the prior, the combined model reveals a stronger association between eCT and cognitive capacity than do nonhierarchical models based on data from single pipelines alone.

stat.AP

Interpretable, similarity-driven multi-view embeddings from high-dimensional biomedical data

Similarity-driven multi-view linear reconstruction (SiMLR) is an algorithm that exploits inter-modality relationships to transform large scientific datasets into smaller, more well-powered and interpretable low-dimensional spaces. SiMLR contributes a novel objective function for identifying joint signal, regularization based on sparse matrices representing prior within-modality relationships and an implementation that permits application to joint reduction of large data matrices, each of which may have millions of entries. We demonstrate that SiMLR outperforms closely related methods on supervised learning problems in simulation data, a multi-omics cancer survival prediction dataset and multiple modality neuroimaging datasets. Taken together, this collection of results shows that SiMLR may be applied with default parameters to joint signal estimation from disparate modalities and may yield practically useful results in a variety of application domains.

stat.ML