Based on results of chaos characteristics comparing one-dimensional iterative chaotic self-map x = sin（2/x） with infinite collapses within the finite region[-1, 1] to some representative iterative chaotic maps with ...Based on results of chaos characteristics comparing one-dimensional iterative chaotic self-map x = sin（2/x） with infinite collapses within the finite region[-1, 1] to some representative iterative chaotic maps with finite collapses （e.g., Logistic map, Tent map, and Chebyshev map）, a new adaptive mutative scale chaos optimization algorithm （AMSCOA） is proposed by using the chaos model x = sin（2/x）. In the optimization algorithm, in order to ensure its advantage of speed convergence and high precision in the seeking optimization process, some measures are taken： 1） the searching space of optimized variables is reduced continuously due to adaptive mutative scale method and the searching precision is enhanced accordingly; 2） the most circle time is regarded as its control guideline. The calculation examples about three testing functions reveal that the adaptive mutative scale chaos optimization algorithm has both high searching speed and precision.展开更多
In order to avoid such problems as low convergent speed and local optimalsolution in simple genetic algorithms, a new hybrid genetic algorithm is proposed. In thisalgorithm, a mutative scale chaos optimization strateg...In order to avoid such problems as low convergent speed and local optimalsolution in simple genetic algorithms, a new hybrid genetic algorithm is proposed. In thisalgorithm, a mutative scale chaos optimization strategy is operated on the population after agenetic operation. And according to the searching process, the searching space of the optimalvariables is gradually diminished and the regulating coefficient of the secondary searching processis gradually changed which will lead to the quick evolution of the population. The algorithm hassuch advantages as fast search, precise results and convenient using etc. The simulation resultsshow that the performance of the method is better than that of simple genetic algorithms.展开更多
Methylmalonic aciduria（MMA） is a common inherited autosomal recessive disorder resulting from defects in the enzyme methylmalonyl CoA mutase（MCM,mut complementation group） or in the synthesis of the MCM cofactor a...Methylmalonic aciduria（MMA） is a common inherited autosomal recessive disorder resulting from defects in the enzyme methylmalonyl CoA mutase（MCM,mut complementation group） or in the synthesis of the MCM cofactor adenosylcobalamin（cbl complementation groups）.The defects in the mut complementation group accounts for the largest number of patients with isolated MMA.At least 200 mutations in the MUT gene on chromosome 6p12 have been identified in MMA patients until now.This study aimed to investigate the clinical characteristics of MMA and genomic variations in the MUT gene of Chinese patients.Genomic DNA was extracted from 18 patients who were diagnosed as having isolated MMA by gas chromatography/mass spectrometry（GC-MS）,and from some of their parents as well.Amplification and direct sequencing of the MUT coding regions（exon 2-13） and their adjacent intronic consensus splice sites were performed in order to identify the disease causing mutations.In this group,six novel mutations in the MUT gene,c.424AG（p.T142A）,c.786TG（p.S262R）,c.808GC（p.G270R）,c.1323_1324insA,c.1445-1GA and c.1676＋77AC were identified.p.T142A and p.G270R were respectively detected at a heterozygous level in one patient.Two previously reported mutations,c.682CT（p.R228X） and c.323GA（p.R108H） were also found in this study.In addition,six previously described single nucleotide polymorphism（SNP）,c.636AG（p.K212K）,c.1495GA（p.A499T）,c.1595AG（p.H532R）,c.1992GA（p.A664A）,c.2011GA（p.V671I） and c.1677-53AG were identified.In this study,we updated the spectrum of MUT mutations and identified the main MMA-causing mutations in Chinese MMA patients.展开更多
基金Hunan Provincial Natural Science Foundation of China (No. 06JJ50103)the National Natural Science Foundationof China (No. 60375001)
文摘Based on results of chaos characteristics comparing one-dimensional iterative chaotic self-map x = sin（2/x） with infinite collapses within the finite region[-1, 1] to some representative iterative chaotic maps with finite collapses （e.g., Logistic map, Tent map, and Chebyshev map）, a new adaptive mutative scale chaos optimization algorithm （AMSCOA） is proposed by using the chaos model x = sin（2/x）. In the optimization algorithm, in order to ensure its advantage of speed convergence and high precision in the seeking optimization process, some measures are taken： 1） the searching space of optimized variables is reduced continuously due to adaptive mutative scale method and the searching precision is enhanced accordingly; 2） the most circle time is regarded as its control guideline. The calculation examples about three testing functions reveal that the adaptive mutative scale chaos optimization algorithm has both high searching speed and precision.
文摘In order to avoid such problems as low convergent speed and local optimalsolution in simple genetic algorithms, a new hybrid genetic algorithm is proposed. In thisalgorithm, a mutative scale chaos optimization strategy is operated on the population after agenetic operation. And according to the searching process, the searching space of the optimalvariables is gradually diminished and the regulating coefficient of the secondary searching processis gradually changed which will lead to the quick evolution of the population. The algorithm hassuch advantages as fast search, precise results and convenient using etc. The simulation resultsshow that the performance of the method is better than that of simple genetic algorithms.
基金supported by grants from the National Basic Research Program of China(2005CB522507)the 11th Five-year Plan of National Science & Technology(2006BAI05A07)
文摘Methylmalonic aciduria（MMA） is a common inherited autosomal recessive disorder resulting from defects in the enzyme methylmalonyl CoA mutase（MCM,mut complementation group） or in the synthesis of the MCM cofactor adenosylcobalamin（cbl complementation groups）.The defects in the mut complementation group accounts for the largest number of patients with isolated MMA.At least 200 mutations in the MUT gene on chromosome 6p12 have been identified in MMA patients until now.This study aimed to investigate the clinical characteristics of MMA and genomic variations in the MUT gene of Chinese patients.Genomic DNA was extracted from 18 patients who were diagnosed as having isolated MMA by gas chromatography/mass spectrometry（GC-MS）,and from some of their parents as well.Amplification and direct sequencing of the MUT coding regions（exon 2-13） and their adjacent intronic consensus splice sites were performed in order to identify the disease causing mutations.In this group,six novel mutations in the MUT gene,c.424AG（p.T142A）,c.786TG（p.S262R）,c.808GC（p.G270R）,c.1323_1324insA,c.1445-1GA and c.1676＋77AC were identified.p.T142A and p.G270R were respectively detected at a heterozygous level in one patient.Two previously reported mutations,c.682CT（p.R228X） and c.323GA（p.R108H） were also found in this study.In addition,six previously described single nucleotide polymorphism（SNP）,c.636AG（p.K212K）,c.1495GA（p.A499T）,c.1595AG（p.H532R）,c.1992GA（p.A664A）,c.2011GA（p.V671I） and c.1677-53AG were identified.In this study,we updated the spectrum of MUT mutations and identified the main MMA-causing mutations in Chinese MMA patients.
