Tensor Neyman-Pearson Classification: Theory, Algorithms, and Error Control

Fuente: arXiv
Enregistré dans:
Détails bibliographiques
Auteurs principaux: Liu, Lingchong, Chen, Elynn, Han, Yuefeng, Xia, Lucy
Format: Preprint
Publié: 2025
Sujets:
Accès en ligne:
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
_version_ 1866914179728801792
author Liu, Lingchong
Chen, Elynn
Han, Yuefeng
Xia, Lucy
author_facet Liu, Lingchong
Chen, Elynn
Han, Yuefeng
Xia, Lucy
contents Biochemical discovery increasingly relies on classifying molecular structures when the consequences of different errors are highly asymmetric. In mutagenicity and carcinogenicity, misclassifying a harmful compound as benign can trigger substantial scientific, regulatory, and health risks, whereas false alarms primarily increase laboratory workload. Modern representations transform molecular graphs into persistence image tensors that preserve multiscale geometric and topological structure, yet existing tensor classifiers and deep tensor neural networks provide no finite-sample guarantees on type I error and often exhibit severe error inflation in practice. We develop the first Tensor Neyman-Pearson (Tensor-NP) classification framework that achieves finite-sample control of type I error while exploiting the multi-mode structure of tensor data. Under a tensor-normal mixture model, we derive the oracle NP discriminant, characterize its Tucker low-rank manifold geometry, and establish tensor-specific margin and conditional detection conditions enabling high-probability bounds on excess type II error. We further propose a Discriminant Tensor Iterative Projection estimator and a Tensor-NP Neural Classifier combining deep learning with Tensor-NP umbrella calibration, yielding the first distribution-free NP-valid methods for multiway data. Across four biochemical datasets, Tensor-NP classifiers maintain type I errors at prespecified levels while delivering competitive type II error performance, providing reliable tools for asymmetric-risk decisions with complex molecular tensors.
format Preprint
id arxiv_https___arxiv_org_abs_2512_04583
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Tensor Neyman-Pearson Classification: Theory, Algorithms, and Error Control
Liu, Lingchong
Chen, Elynn
Han, Yuefeng
Xia, Lucy
Methodology
62H30 (Primary) 15A69, 68T07, 62F12 (Secondary)
I.5.1; I.5.2
Biochemical discovery increasingly relies on classifying molecular structures when the consequences of different errors are highly asymmetric. In mutagenicity and carcinogenicity, misclassifying a harmful compound as benign can trigger substantial scientific, regulatory, and health risks, whereas false alarms primarily increase laboratory workload. Modern representations transform molecular graphs into persistence image tensors that preserve multiscale geometric and topological structure, yet existing tensor classifiers and deep tensor neural networks provide no finite-sample guarantees on type I error and often exhibit severe error inflation in practice. We develop the first Tensor Neyman-Pearson (Tensor-NP) classification framework that achieves finite-sample control of type I error while exploiting the multi-mode structure of tensor data. Under a tensor-normal mixture model, we derive the oracle NP discriminant, characterize its Tucker low-rank manifold geometry, and establish tensor-specific margin and conditional detection conditions enabling high-probability bounds on excess type II error. We further propose a Discriminant Tensor Iterative Projection estimator and a Tensor-NP Neural Classifier combining deep learning with Tensor-NP umbrella calibration, yielding the first distribution-free NP-valid methods for multiway data. Across four biochemical datasets, Tensor-NP classifiers maintain type I errors at prespecified levels while delivering competitive type II error performance, providing reliable tools for asymmetric-risk decisions with complex molecular tensors.
title Tensor Neyman-Pearson Classification: Theory, Algorithms, and Error Control
topic Methodology
62H30 (Primary) 15A69, 68T07, 62F12 (Secondary)
I.5.1; I.5.2
url https://arxiv.org/abs/2512.04583