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Alif Tahmid Priyom

Publications and source records attributed to Alif Tahmid Priyom.

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Spatial Neighboring Scattering Transform: A Cross-Channel Amplitude Coupling Measure for EEG Connectivity

The functional organization of the brain relies on coordinated activity across spatially distributed regions, making the analysis of inter-regional dependencies fundamental. Existing connectivity measures address this predominantly through phase synchronization, which is vulnerable to volume conduction artifacts and discards amplitude-domain coupling. This study introduces the Spatial Neighboring Scattering Transform, which extends the wavelet scattering transform to the multichannel setting, yielding two descriptors that jointly capture amplitude-envelope coupling between channels and its modulation across frequency scales. SNST was evaluated on the BCI Competition IV-2a motor imagery dataset using a bias-corrected, false-discovery-rate-controlled statistical pipeline, with the validation criterion defined as spatial consistency of significant coupling across subjects. The first-order descriptor identified statistically significant amplitude coupling within a central-parietal electrode neighborhood, reproduced consistently across all subjects and both imagery conditions. The second-order descriptor revealed that this coupling is periodically gated by slow rhythms, indicating a cross-frequency amplitude-modulation structure absent from single-frequency connectivity measures. Phase lag index and weighted phase lag index, computed under an identical correction procedure and verified robust to volume conduction, identified negligible significant coupling with zero overlap with SNST findings, demonstrating that amplitude envelope coupling constitutes a largely distinct connectivity signal. These results establish SNST as a cross-channel scattering-based connectivity descriptor that recovers amplitude-envelope and cross-frequency coupling structure systematically, applicable to any multichannel EEG analysis where amplitude-domain inter-regional dependence is of interest.

q-bio.NC

Wavelet Scattering Transform for Interpretable Schizophrenia Biomarker Discovery and Classification from Resting-State EEG

Schizophrenia is a debilitating neuropsychiatric disorder characterized by profound cortical network dysregulation, for which objective, clinically translatable EEG based biomarkers remain underdeveloped. Existing automated classification pipelines rely predominantly on static power spectral density features inherently blind to amplitude modulation dynamics and cross-frequency coupling, phenomena central to schizophrenia pathophysiology, while adopting epoch level cross validation strategies that introduce temporal data leakage, artificially inflate reported performance. This study introduces a mathematically principled diagnostic framework integrating the multi-order Wavelet Scattering Transform(WST), strict Leave One Subject Out (LOSO) cross-validation, and SHAP explainability for simultaneous EEG classification and biomarker discovery. Hierarchical WST coefficients capturing multi-scale amplitude modulation structure were extracted from resting state multichannel EEG. Subject-level ANOVA with Benjamini Hochberg false discovery rate correction identified significant biomarkers, with Random Forest and SVM classifiers evaluated under strict LOSO cross validation and subject-level majority voting. Second-order scattering coefficients encoding cross frequency coupling dominated the discriminative biomarker set, with gamma-band features most prevalent, demonstrating that temporal amplitude modulation constitutes the primary electrophysiological signature of schizophrenia. Electrode P3 was identified as the single most discriminative site. Under rigorous subject independent evaluation, the Random Forest achieved 90.48% accuracy (AUC = 0.9339; sensitivity = 95.56%). The proposed WST framework establishes a rigorous, interpretable standard for EEG-driven psychiatric biomarker discovery that can also be applicable in the detection of schizophrenia subtypes in the future.

eess.SP