<p>The early identification of Autism Spectrum Disorder (ASD) remains a critical challenge in neurodevelopmental research, with current diagnostic processes often delayed by subjective assessments and limited clinical resources. This paper presents a memory-efficient Neural Architecture Search framework that autonomously identifies optimum neural network structures for ASD classification. Unlike existing genetic algorithm-based NAS approaches requiring over 16GB GPU memory, our framework achieves 76% memory reduction while maintaining superior performance. Our approach presents three key innovations: (1) a novel search space integrating simple, residual, and bottleneck operations with <InlineEquation ID="IEq1"> <EquationSource Format="TEX">\({\mathcal {O}}(3^L)\)</EquationSource> </InlineEquation> complexity for <i>L</i> layers; (2) a memory-efficient genetic algorithm that decreases GPU memory consumption by <InlineEquation ID="IEq2"> <EquationSource Format="TEX">\(76\%\)</EquationSource> </InlineEquation> relative to current methodologies while preserving search efficacy; and (3) an adaptive fitness function that equilibrates model performance with computational complexity. Through comprehensive experiments utilizing a substantial dataset (<InlineEquation ID="IEq3"> <EquationSource Format="TEX">\(N = 1,262,856\)</EquationSource> </InlineEquation>; <InlineEquation ID="IEq4"> <EquationSource Format="TEX">\(n_{ASD} = 501,733\)</EquationSource> </InlineEquation>, <InlineEquation ID="IEq5"> <EquationSource Format="TEX">\(n_{TD} = 502,541\)</EquationSource> </InlineEquation>), our methodology attained a classification accuracy of <InlineEquation ID="IEq6"> <EquationSource Format="TEX">\(95.23\%\)</EquationSource> </InlineEquation> (<InlineEquation ID="IEq7"> <EquationSource Format="TEX">\(95\%\)</EquationSource> </InlineEquation> CI: 94.89-<InlineEquation ID="IEq8"> <EquationSource Format="TEX">\(95.57\%\)</EquationSource> </InlineEquation>) and area under the Receiver Operating Characteristic (ROC) curve of 0.986, which markedly surpassed existing state-of-the-art techniques (traditional CNN: 92.3%, ResNet-based: 94.1%, LSTM: 93.7%). The framework achieves this performance with 2.8M parameters and 15ms processing time per sample, demonstrating practical viability for clinical deployment in resource-constrained settings where current diagnostic procedures extend 4-5 years after symptom onset.</p>

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GeneticNAS: a novel self-evolving neural architecture for advanced ASD screening

  • Abdullah R. Alzahrani,
  • Dabiah Alboaneen,
  • Ibrahim R. Alzahrani

摘要

The early identification of Autism Spectrum Disorder (ASD) remains a critical challenge in neurodevelopmental research, with current diagnostic processes often delayed by subjective assessments and limited clinical resources. This paper presents a memory-efficient Neural Architecture Search framework that autonomously identifies optimum neural network structures for ASD classification. Unlike existing genetic algorithm-based NAS approaches requiring over 16GB GPU memory, our framework achieves 76% memory reduction while maintaining superior performance. Our approach presents three key innovations: (1) a novel search space integrating simple, residual, and bottleneck operations with \({\mathcal {O}}(3^L)\) complexity for L layers; (2) a memory-efficient genetic algorithm that decreases GPU memory consumption by \(76\%\) relative to current methodologies while preserving search efficacy; and (3) an adaptive fitness function that equilibrates model performance with computational complexity. Through comprehensive experiments utilizing a substantial dataset ( \(N = 1,262,856\) ; \(n_{ASD} = 501,733\) , \(n_{TD} = 502,541\) ), our methodology attained a classification accuracy of \(95.23\%\) ( \(95\%\) CI: 94.89- \(95.57\%\) ) and area under the Receiver Operating Characteristic (ROC) curve of 0.986, which markedly surpassed existing state-of-the-art techniques (traditional CNN: 92.3%, ResNet-based: 94.1%, LSTM: 93.7%). The framework achieves this performance with 2.8M parameters and 15ms processing time per sample, demonstrating practical viability for clinical deployment in resource-constrained settings where current diagnostic procedures extend 4-5 years after symptom onset.