• Title/Summary/Keyword: Genetic influence

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Balancing of a Rigid Rotor using Genetic Algorithms (유전 알고리즘을 이용한 강성회전체의 평형잡이)

  • Yang, Bo Seok;Ju, Ho Jin
    • Journal of Advanced Marine Engineering and Technology
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    • v.20 no.2
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    • pp.108-108
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    • 1996
  • This paper describes a new approach to solve balancing of a rigid rotor. In this paper, the balancing of the rigid rotor using genetic algorithms, which are search algorithms based on the mechanics of natural selection and natural genetics is proposed. Under the assumption that the initial vibration values used to calculate correction masses contain errors, the influence coefficient method, the least squares method and a genetic algorithm are compared. The results show that the vibration amplitude obtained with the least squares method and the genetic algorithm is smaller than that obtained with the influence coefficient method.

Balancing of a Rigid Rotor using Genetic Algorithms (유전 알고리즘을 이용한 강성회전체의 평형잡이)

  • 양보석;주호진
    • Journal of Advanced Marine Engineering and Technology
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    • v.20 no.2
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    • pp.40-47
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    • 1996
  • This paper describes a new approach to solve balancing of a rigid rotor. In this paper, the balancing of the rigid rotor using genetic algorithms, which are search algorithms based on the mechanics of natural selection and natural genetics is proposed. Under the assumption that the initial vibration values used to calculate correction masses contain errors, the influence coefficient method, the least squares method and a genetic algorithm are compared. The results show that the vibration amplitude obtained with the least squares method and the genetic algorithm is smaller than that obtained with the influence coefficient method.

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Parameter Optimization of QUAL2K Using Influence Coefficient Algorithm and Genetic Algorithm (영향계수법과 유전알고리즘을 이용한 QUAL2K 모형의 매개변수 최적화)

  • Cho, Jae-Heon;Lee, Chang-Hun
    • Journal of Environmental Impact Assessment
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    • v.18 no.2
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    • pp.99-109
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    • 2009
  • In general, manual calibration is commonly used for the stream water quality modelling. Because the manual calibration depends upon the subjectivity and experience of the researcher, it has a problem with the objectivity of the modelling. Thus, the interest about the automatic calibration by the optimization technique is deeply increased. In this study, Influence coefficient algorithm and Genetic algorithm are introduced to develop an automatic calibration model for the QUAL2K that are the latest version of the QUAL2E. Genetic algorithm, used in this study, is very simple and easy to understand but also applicable to any complicated mathematical problem, and it can find out the global optimum solution effectively. The developed automatic calibration model is applied to the Gangneung Namdaecheon. The calibration results about the 11 water quality variables show the good correspondence between the calculated and observed water quality values.

Genomic Susceptibility Analysis for Atopy Disease Using Cord Blood DNA in a Small Cohort

  • Koh, Eun Jung;Kim, Seung Jun;Ahn, Jeong Jin;Yang, Jungeun;Oh, Moon Ju;Hwang, Seung Yong
    • BioChip Journal
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    • v.12 no.4
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    • pp.304-308
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    • 2018
  • Atopic disease is caused by a complex combination of environmental factors and genetic factors, and studies on influence of exposure to various environmental factors on atopic diseases are continuously reported. However, the exact cause of atopic dermatitis is not yet known. Our study was conducted to analyse the association of SNPs with the development of atopic disease in a small cohort. Samples were collected from the Mothers' and Children's Environmental Health (MOCEH) study and 192 cord blood DNA samples were used to identify incidence of atopy due to influence of exposure to environmental factors. Genetic elements were analysed using a precision medicine research (PMR) array designed with various SNPs for personalized medicine. Case-control analysis of atopy disease revealed 253 significant variants (p<0.0001) and SNPs on five genes (CARD11, ZNF365, KIF3A, DMRTA1, and SFMBT1) were variants identified in previous atopic studies. These results are important to confirm the genetic mutation that may lead to the onset of foetal atopy due to maternal exposure to harmful environmental factors. Our results also suggest that a small-scale genome-wide association analysis is beneficial to confirm specific variants as direct factors in the development of atopy.

Bitter Taste Receptor TAS2R38 Genetic Variation (rs10246939), Dietary Nutrient Intake, and Bio-Clinical Parameters in Koreans

  • Benish;Jeong-Hwa Choi
    • Clinical Nutrition Research
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    • v.12 no.1
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    • pp.40-53
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    • 2023
  • Differential bitterness perception associated with genetic polymorphism in the bitter taste receptor gene taste 2 receptor member 38 (TAS2R38) may influence an individual's food preferences, nutrition consumption, and eventually chronic nutrition-related disorders including cardiovascular disease. Therefore, the effect of genetic variations on nutritional intake and clinical markers needs to be elaborated for health and disease prevention. In this study, we conducted sex-stratified analysis to examine the association between genetic variant TAS2R38 rs10246939 A > G with daily nutritional intake, blood pressure, and lipid parameters in Korean adults (males = 1,311 and females = 2,191). We used the data from the Multi Rural Communities Cohort, Korean Genome and Epidemiology Study. Findings suggested that the genetic variant TAS2R38 rs10246939 was associated with dietary intake of micronutrients including calcium (adjusted p = 0.007), phosphorous (adjusted p = 0.016), potassium (adjusted p = 0.022), vitamin C (adjusted p = 0.009), and vitamin E (adjusted p = 0.005) in females. However, this genetic variant did not influence blood glucose, lipid profile parameters, and other blood pressure markers. These may suggest that this genetic variation is associated with nutritional intake, but its clinical effect was not found. More studies are needed to explore whether TAS2R38 genotype may be a potential predictive marker for the risk of metabolic diseases via modulation of dietary intake.

Estimates of Genetic Parameters and Genetic Trends for Production Traits of Inner Mongolian White Cashmere Goat

  • Bai, Junyan;Zhang, Qin;Li, Jinquan;Dao, Er-Ji;Jia, Xiaoping
    • Asian-Australasian Journal of Animal Sciences
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    • v.19 no.1
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    • pp.13-18
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    • 2006
  • Two different animal models, which differ in whether or not taking maternal genetic effect into account, for estimating genetic parameters of cashmere weight, live body weight, cashmere thickness, staple length, fiber diameter, and fiber length in Inner Mongolia White Cashmere Goat were compared via likelihood ratio test. The results indicate that maternal genetic effect has significant influence on live body weight and cashmere thickness, but no significant influence on the other traits. Using models suitable for each trait, both genetic parameters and trends were analyzed with the MTDFREML program. Heritability estimates from single trait models for cashmere weight, live body weight, cashmere thickness, staple length, fiber diameter and fiber length were found to be 0.30, 0.07, 0.21, 0.29, 0.28 and 0.21, respectively. Genetic correlation estimates from two-trait models between live body weight and all other traits (-0.06~0.07) was negligible, as were those between fiber diameter and all other traits (-0.01~0.03) except cashmere thickness (0.19). Cashmere weight and staple length had moderate to low genetic correlations with other traits (-0.24~0.39 and -0.24~0.34, respectively) except for live body weight and fiber diameter. Cashmere thickness had a strong genetic correlation with fiber length (0.81), and low genetic correlation with other traits (0.19~0.34) except live body weight. Genetic trend analysis suggests that selection for cashmere weight was very effective, which has led to the slow genetic progress of cashmere thickness and fiber length due to their genetic correlations with cashmere weight. The selection for live body weight was not effective, which was consistent with its low inheritability.

Optimum Field Balancing of Ratating Machinery Using Genetic Algorithm (유전 알고리즘을 이용한 회전기계의 최적 현장평형잡이)

  • Choi, Won-Ho;Yang, Bo-Suk;Joo, Ho-Jin
    • Transactions of the Korean Society of Mechanical Engineers A
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    • v.20 no.6
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    • pp.1819-1826
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    • 1996
  • This paper present the claculating method of optimum correction mass within permissible vibration linits for ratating machinery in two-plane field balancing. Basic technique of this method is based on influence coefficient method, and grphic vector composition that the resultant of two influence vectors obtained by trial mass have to be equilibrium with initial vibration vector in the each correction plane. Genetic algorithm which is a search algorithm based on the mechanism of natural selection and natural genetics is sued for vector composition, and SUMT method is used to objective function which seeks optimum correction mass for balancing a rotor.

Optimum Balancing of Rotating Machinery Using Genetic Algorithm (유전 알고리즘을 이용한 회전기계의 최적 평형잡이)

  • 주호진;최원호;양보석
    • Proceedings of the Korean Institute of Intelligent Systems Conference
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    • 1995.10b
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    • pp.195-202
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    • 1995
  • This paper presents the calculating method of optimum correction mass within permissible vibration limits for rotating machinery in two-plane field balancing. Basic technique of this method based on influence coefficient method, is graphic vector composition that the resultant of two influence vectors obtained by trial mass have to be equilibrium with initial vibration vector in the each correction plane. Genetic algorithm which is a search algorithm based on the mechanics of natural selection and natural genetics is used for vector composition, and SUMT method is used to objective function which seeks optimum correction mass for balancing a rotor.

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Association Between Genetic Polymorphism of XRCC1 Gene and Risk of Glioma in а Chinese Population

  • Wang, Ying-Xin;Fan, Kai;Tao, Ding-Bo;Dong, Xiang
    • Asian Pacific Journal of Cancer Prevention
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    • v.14 no.10
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    • pp.5957-5960
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    • 2013
  • Background: Gliomas are the most common type of primary brain tumor in adults, and the X-ray repair complementing group 1 gene (XRCC1) is an important candidate gene influencing its risk. The objective of this study was to detect the influence of XRCC1 genetic polymorphisms on glioma risk. Materials and Methods: A total of 629 glioma patients and 641 cancer-free subjects were enrolled in this case-control study. The genotypes of the c.1471G>A genetic polymorphism were determined by created restriction site-polymerase chain reaction (CRS-PCR) and DNA sequencing methods. The influence of the XRCC1 genetic polymorphism on glioma risk was evaluated by association analysis. Results: Our data indicated that the alleles/genotype of this genetic variant was statistically associated with glioma risk. The AA genotype was statistically associated with the increased risk of glioma compared to the GG wild genotype (odds ratios (OR) = 1.89, 95% CI 1.25-2.87, P = 0.003). The allele-A may contribute to increased the susceptibility to glioma (OR = 1.23, 95% CI 1.04-1.46, P = 0.017). Conclusions: These preliminary findings indicate that the c.1471G>A genetic polymorphism of XRCC1 has the potential to influence glioma susceptibility, and might be used as molecular marker for assessing glioma risk.

Social Determinants of Smoking Behavior: The Healthy Twin Study, Korea

  • Kim, Youn-Sik;Ko, Han-Soo;Yoon, Chang-Gyo;Lee, Dong-Hun;Sung, Joo-Hon
    • Journal of Preventive Medicine and Public Health
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    • v.45 no.1
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    • pp.29-36
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    • 2012
  • Objectives: The purpose of this study was to identify any influence of socioeconomic status on smoking and smoking cessation in a situation where genetic factors are controlled. Methods: The sample for this study was 2502 members of the twins and families cohort who participated in the Korean Healthy Twins Study from 2005 to 2009. Groups of brothers or sisters, including twins and fraternal twins, were compared in terms of smoking and smoking cessation behaviors according to differences in socioeconomic status and gender. Results: In a situation with complete control of genetic factors, results showed that the daily smoking amount, cumulative smoking amount, and dependence on nicotine decreased with higher-status occupations, and the rate of smoking and amount of cumulative smoking decreased with higher levels of education. Regarding smoking cessation behavior, a higher level of education was associated with a lower smoking cessation rate, and no significant gender differences were found. Conclusions: Environmental factors had a stronger influence on smoking behavior than did genetic factors. Genetic factors had greater influence on smoking cessation than did environmental factors; however, this requires verification in further studies.