Biosignal Quality Evaluation Using Frequency-Domain Spectral Morphology

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Solution Overview

Problem

Existing methods for evaluating biosignal quality, such as signal-to-noise ratio (SNR), are inadequate for biosignals due to difficulties in defining alternating current (AC) and direct current (DC) components, making it challenging to assess biosignal quality accurately in real-world environments.

Innovation Solution

A device and method that normalize biosignals, convert them into the frequency domain, and extract morphological features to evaluate quality by dividing the spectrum into regions and using morphological features like maximum, minimum, skewness, and frequency band ratios.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If signal-to-noise ratio (SNR) is used to evaluate biosignal quality, then evaluation can be performed using conventional methods, but accurate quality assessment becomes difficult due to inability to define AC and DC components in biosignals

Engineering Contradiction:
Improveease of quality evaluationVSAvoidquality assessment accuracy
Core Design Contradiction:
Ease of manufactureVSMeasurement precision

Solution Approach 1:

The patent transforms the quality evaluation from time domain parameters (AC/DC ratio) to frequency domain parameters (spectral morphology features). By converting biosignals to frequency domain and analyzing spectral characteristics such as peak frequency, bandwidth, and spectral entropy, the method enables accurate quality assessment without needing to define ambiguous AC/DC components in biosignals.

Inventive Principle:
Principle #35Parameter changes

2Object-affected harmful factors

If filtering techniques are applied to remove noise from biosignals, then noise reduction can be achieved, but signal quality evaluation remains challenging due to lack of appropriate metrics

Engineering Contradiction:
Improvenoise levelVSAvoidquality evaluation accuracy
Core Design Contradiction:
Object-affected harmful factorsVSMeasurement precision

Solution Approach 1:

The patent implements a feedback mechanism where spectral morphology features are extracted from filtered biosignals to evaluate the effectiveness of noise removal. By continuously monitoring frequency domain characteristics such as spectral power distribution and morphological features, the system provides feedback on signal quality, enabling adaptive filtering and accurate quality assessment.

Inventive Principle:
Principle #23Feedback

3Device complexity

If conventional SNR calculation methods are used, then evaluation process is simple, but the method is inappropriate for actual biosignal measurement environments

Engineering Contradiction:
Improveevaluation process complexityVSAvoidevaluation reliability
Core Design Contradiction:
Device complexityVSReliability

Solution Approach 1:

The patent moves the evaluation from one-dimensional time domain analysis to two-dimensional frequency domain analysis. By examining spectral morphology across different frequency components and extracting multiple features (peak frequency, bandwidth, spectral entropy), the method provides more reliable quality assessment that accounts for the complex characteristics of biosignals in actual measurement environments.

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

Data Source

PatentUS20250366790A1Device and method for evaluating quality of biosignal
Publication Date: 2025.12.04 ELECTRONICS & TELECOMM RES INST
  • US20250366790A1 patent drawing
  • US20250366790A1 patent drawing
  • US20250366790A1 patent drawing

AI summary

Provided are a device and method for evaluating quality of a biosignal. The device includes a processor and a memory which stores instructions executed by the processor. The processor normalizes a biosignal and converts the normalized biosignal into a frequency domain, extracts a morphological feature of a spectrum in the frequency domain, and evaluates quality of the biosignal on the basis of the morphological feature.