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Bangera, S. C.

Publications and source records attributed to Bangera, S. C..

2 recordsLinked to original sources

MORPH2DIAG: Automated Structural MRI Preprocessing and Tissue Segmentation for Interpretable Machine and Deep Learning-Based Neuroanatomical Classification

Structural MRI provides a noninvasive window into brain morphology, yet the reproducibility and interpretability of morphometric analyses remain limited by inconsistent preprocessing, variable spatial alignment, and heterogeneous feature construction. We introduce MORPH2DIAG, a fully automated, atlas-free morphometric pipeline that integrates standardized preprocessing, tissue segmentation, spatial normalization, data-driven subtyping, and machine- and deep-learning classification within a single, modular framework. The pipeline performs intensity normalization, morphological cleanup, PCA-informed affine alignment, isotropic rescaling, and Gaussian Mixture Model (GMM) segmentation to generate quantitative gray-matter (GM), white-matter (WM), and cerebrospinal-fluid (CSF) maps. Global tissue fractions were used to derive latent neuroanatomical subtypes via unsupervised K-means clustering, revealing progressive GM-CSF gradients consistent with patterns commonly observed along normative-to-atrophic structural continua observed in neurodegeneration. To capture finer-grained spatial heterogeneity, a voxel-wise K-means parcellation yielded parcel-level intensity means and variances that served as regional morphometric descriptors. These global and parcel-level features were integrated into a unified evaluation suite comparing classical machine learning models (Random Forests, Logistic Regression, XGBoost) with lean, deep, and hybrid multilayer perceptrons (MLPs) trained using focal loss, label smoothing, stochastic weight averaging, and nested cross-validation with PCA-based dimensionality reduction. Across methods, the hybrid MLP achieved the highest macro-F1 and balanced accuracy, demonstrating strong discriminative performance for the discovered morphometric subtypes. Collectively, MORPH2DIAG establishes a fully automated, atlas-free framework that unites unsupervised structural subtype discovery with interpretable machine and deep learning, providing a reproducible foundation for MRI-based morphometric profiling and automated detection of neurodegenerative-like patterns.

neuroscience↗

Decoding hidden goal-directed navigational states and their neuronal representations using a novel labyrinth paradigm and probabilistic modeling framework

Goal-directed navigation involves a sequence of planned actions aimed at achieving long-term goals through reinforcement, but detecting hidden states that support this process and their neuronal substrates remains a fundamental challenge. To address this, we developed a complex labyrinth test that mimics naturalistic foraging and implemented a novel hierarchical probabilistic modeling framework, Cognitive Mapping of Planned Actions with State Spaces (CoMPASS). This framework infers a nested state structure, comprising short-term surveillance-ambulation states (Level 1) and long-term goal-oriented navigational states (Level 2). Using CoMPASS, we show that successful navigation in wild-type mice is marked by increased recruitment of both surveillance and goal-oriented states specifically at decision nodes, revealing how sequential behavioral decisions culminate in long-term goals. In contrast, the humanized AppSAA mouse model of Alzheimers disease (AD) exhibited navigational impairments marked by diminished surveillance during decisions, reduced goal-directed states, and increased navigation stochasticity. Importantly, we show that gamma oscillations in the posterior parietal cortex (PPC), a region involved in spatial navigation planning, encode these CoMPASS behavioral states and their dynamic operating modes linking spatial locations to long-term goals. Our findings provide a novel paradigm for assessing hidden goal-directed navigational states and identify gamma oscillations in the PPC as their neural substrates.

neuroscience↗