Method for screening hepatic disease marker from body fluid metabolic profile using chain multi-population genetic algorithm

A genetic algorithm and body fluid metabolism technology, applied in the field of screening small molecule metabolic markers of liver disease, can solve the problems of reduced population diversity and easy to fall into local optimum, and achieve accurate feature importance measurement, short sample analysis time and high reliability Effect

Inactive Publication Date: 2010-12-01
DALIAN UNIV OF TECH
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Problems solved by technology

[0006] The genetic algorithm has a strong dependence on the initial population. In the iterative process, with the con

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  • Method for screening hepatic disease marker from body fluid metabolic profile using chain multi-population genetic algorithm
  • Method for screening hepatic disease marker from body fluid metabolic profile using chain multi-population genetic algorithm
  • Method for screening hepatic disease marker from body fluid metabolic profile using chain multi-population genetic algorithm

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[0037] Embodiments of the present invention will be described in detail below in conjunction with the accompanying drawings. The present embodiment is implemented under the guidance of the technical solution of the present invention, but the protection scope of the present invention is not limited to the following embodiments, and the following embodiments are only used as examples of the present invention rather than limitation. Without violating the gist and scope of the present invention, various changes and improvements can be made to the present invention, but all these changes and improvements should be within the protection scope of the present invention. Example: Screening of liver disease markers based on plasma metabolic profile.

[0038] (1) Collection and pretreatment of human plasma samples.

[0039] Blood samples from 99 patients with liver disease. Among them, there were 26 cases of hepatitis, 28 cases of liver cirrhosis, and 45 cases of liver cancer. The coll...

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Abstract

The invention provides a method for screening a hepatic disease marker from a body fluid metabolic profile using a chain multi-population genetic algorithm, belonging to the data mining and metabonimics technical field. The method is characterized by comprising the following steps: firstly, analyzing body fluid metabolites using a liquid chromatograph-mass spectrometer (LC-MS) to obtain the metabolic profile, carrying out multi-population parallel evolution to obtain a plurality of feature subsets with strong discrimination capability, and measuring significance of features according to the frequency that the features appear in the subsets; secondly, searching from front to back according to the significance of the features sequentially to screen out the marker showing three-stage specificity of hepatic disease; and finally carrying out information interaction between adjacent populations during the evolution to avoid a premature defect of the genetic algorithm. Meanwhile, the invention further provides a new crossover operation to ensure that any chromosome does not contain the same feature. The method can help efficiently and accurately screen out the relevant markers in three stages of hepatic disease, thus achieving high precision and good stability; and 10-fold cross validation for a SVM model constructed by the screened features can achieve up to 97.9% in high precision.

Description

technical field [0001] The invention belongs to the technical fields of data mining and metabolomics, and is a new method for screening small molecular metabolic markers of liver disease by analyzing the metabolic profile of body fluids based on the data mining method and metabolomics technology. Background technique [0002] Liver disease has increasingly become one of the diseases that seriously endanger human health. According to the statistics of the World Health Organization, there are about 350 million people with chronic hepatitis infection in the world. In the course of the disease, chronic hepatitis can develop into liver cirrhosis, which is one of the main causes of hepatocellular carcinoma (HCC). Chronic hepatitis, liver cirrhosis, and liver cancer caused by HBV infection cause 500,000 to 1,200,000 deaths per year. Worldwide, the mortality rate of liver cancer patients ranks fourth among malignant tumors. In China, since the 1990s, the mortality rate of liver can...

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Application Information

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IPC IPC(8): G06F19/00
Inventor 林晓惠李红尹佩源许国旺
Owner DALIAN UNIV OF TECH
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