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A novel hybrid model integrating MFCC and acoustic parameters for voice disorder detection. | LitMetric

A novel hybrid model integrating MFCC and acoustic parameters for voice disorder detection.

Sci Rep

Department of Electronic Engineering and Computer Science, School of Science and Technology, Hong Kong Metropolitan University (HKMU), Kowloon, Hong Kong.

Published: December 2023

AI Article Synopsis

  • Voice is crucial for human communication, and disruptions in vocal fold vibrations can lead to serious voice disorders that impact social interactions.
  • Early detection of these disorders is essential for improving overall voice health and quality of life.
  • The proposed method, VDDMFS, utilizes a combination of artificial neural networks and LSTM models for accurate detection of voice disorders, achieving high performance with an accuracy of 95.67% and outperforming current techniques.

Article Abstract

Voice is an essential component of human communication, serving as a fundamental medium for expressing thoughts, emotions, and ideas. Disruptions in vocal fold vibratory patterns can lead to voice disorders, which can have a profound impact on interpersonal interactions. Early detection of voice disorders is crucial for improving voice health and quality of life. This research proposes a novel methodology called VDDMFS [voice disorder detection using MFCC (Mel-frequency cepstral coefficients), fundamental frequency and spectral centroid] which combines an artificial neural network (ANN) trained on acoustic attributes and a long short-term memory (LSTM) model trained on MFCC attributes. Subsequently, the probabilities generated by both the ANN and LSTM models are stacked and used as input for XGBoost, which detects whether a voice is disordered or not, resulting in more accurate voice disorder detection. This approach achieved promising results, with an accuracy of 95.67%, sensitivity of 95.36%, specificity of 96.49% and f1 score of 96.9%, outperforming existing techniques.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10733415PMC
http://dx.doi.org/10.1038/s41598-023-49869-6DOI Listing

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