Masterarbeit, 2014
76 Seiten
CHAPTER-1 Background
1.1 Introduction
1.2 Diagnosis of Allergic Diseases
1.3 Research Status
1.4 In-vitro Allergy Test Products
CHAPTER 2 In-Vitro Allergen Testing Device
2.1 Preparation of Reagent
2.2 Experimental Device
2.3 System Assembly
Chapter 3 Verification of System Stability and Grayscale Image Analysis
3.1 Introduction
3.2 Color calibration of the imaging system by intensity ratio analysis
3.3 Gray Value Analysis of Colored Reaction Product
CHAPTER 4 COLOR MODELS AND IMAGE ANALYSIS
4.1 Introduction
4.2 Color Models
5. Polynomial Regression
5.1 Background
5.2 Null hypothesis
5.3 Experiment Motive
5.4 Procedure Details
6. Summary and Future Work
7. References
This thesis aims to develop an automatic and quantitative IgE concentration detection algorithm for use in a self-designed allergen disease diagnosis system. By utilizing image processing techniques on ELISA reagent strips, the research seeks to create a cost-effective, sensitive, and reproducible method for allergy diagnosis that overcomes the limitations of manual qualitative assessments.
3.3.4.5 Color Difference Signal
Considering the color of the reagent strip is green and blue in white light then the green-blue color of the allergen card tends to be higher with high IgE concentration. Higher the concentration of IgE, greater will be the contribution of the green and blue channel. So at the higher IgE concentration, scanning of the allergen block at single wavelength may be difficult to separate different color products from one another. Hence, it is expected to use B and G signal channel and the difference signal channel. For the analysis of the cat allergen data, G channel wavelength is around 530-550 nm and the B channel wavelength is around 430-450 nm. The G channel is set to value a, and the B channel to value b.
The color difference at the characteristic signal value, denoted by T is given by the formula T = b*X*a, where X is the color coefficient. Color difference results in a high concentration (21.09 ~ 60.27IU/ml) is monotonically increasing with highest sensitivity, expressed as the maximum slope. Then b*x*a formula is extracted. Experimental results show that, x = 5.5, a is 430nm, b is the maximum slope of the color difference signal 550nm. Inversely, for the low concentration IgE sample light wavelength 610 nm is sensitive. So for the low IgE concentration sample, characteristic signal value is estimated at 610 nm wavelength light.
CHAPTER-1 Background: This chapter provides an overview of allergic diseases, their global prevalence, and current diagnostic methodologies including Skin Prick Tests and ELISA.
CHAPTER 2 In-Vitro Allergen Testing Device: This section details the experimental design, including the preparation of reagent strips and the assembly of the imaging system.
Chapter 3 Verification of System Stability and Grayscale Image Analysis: This chapter covers the calibration of the imaging setup to ensure system stability and introduces the processing of grayscale images for data collection.
CHAPTER 4 COLOR MODELS AND IMAGE ANALYSIS: This chapter investigates various color models such as RGB, YUV, and YCbCr to identify optimal features for quantifying IgE concentration.
5. Polynomial Regression: This chapter discusses the use of polynomial regression models to establish a reliable relationship between independent IgE concentration variables and dependent image feature responses.
6. Summary and Future Work: This chapter concludes the research by summarizing the developed methods and proposing directions for future improvements in automated allergy diagnostics.
Allergic disease, Automatic Diagnosis, IgE, ELISA, Quantitative Detection, Image Processing, Color Models, Polynomial Regression, Reagent Strip, Allergen, Multispectral Imaging, G Channel, Machine Vision, Sensitivity, Immunoassay.
The research focuses on developing an automatic and quantitative tool for measuring IgE concentration to improve the diagnosis of allergic diseases using image processing.
The study utilizes the Enzyme-linked Immuno-Sorbent Assay (ELISA) technique performed on paper reagent strips as the basis for color-based detection.
The objective is to replace manual qualitative observation with an accurate, quantitative, and reproducible automated system for analyzing IgE-induced color intensity.
The research employs multispectral imaging, image feature extraction from various color models, and polynomial regression to map image features to IgE concentration levels.
It covers the experimental hardware setup, calibration procedures, the evaluation of different color spaces, and the development of regression curves to quantify serum IgE.
Key terms include Allergic disease, Automatic Diagnosis, IgE, ELISA, Quantitative Detection, Image Processing, and Polynomial Regression.
The study investigates the impact of wet versus dry conditions on color intensity and explores image features and algorithms to compensate for these environmental differences.
Different color models are analyzed to find an image feature that is monotonic, sensitive, and stable across various environmental conditions to ensure reliable quantification.
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